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This page was generated using the FutureHouse Falcon deep search tool in response to the following query: "What are the various ways in which synthetic cells (also called artificial cells) can be supplied with energy, to allow operation of genetic circuits and/or protein expression to be carried out for longer period of time." The text was then rearranged and edited to provide more structure and context. | This page was originally generated using the [https://platform.futurehouse.org FutureHouse Falcon] deep search tool in response to the following query: "What are the various ways in which synthetic cells (also called artificial cells) can be supplied with energy, to allow operation of genetic circuits and/or protein expression to be carried out for longer period of time." The text was then rearranged and edited to provide more structure and context. The page was further modified based on the paper [[Engineering Biology at Scale Using Synthetic Cells: A Systems and Control Perspective]] (Murray, 2026), using Claude Code to assist with integration and formatting. This page was reviewed by the author on 27 Jun 2026. | ||
== Overview == | == Overview == | ||
The metabolic subsystem provides the energy required for a synthetic cell to operate. Even modest genetic circuits and actuation modules can rapidly exhaust the energy resources available in a closed cell-free system, causing shutdown on the timescale of hours<ref name="Jewett2004" />. As a result, energy supply should be viewed not as an auxiliary concern but as a core enabling service whose design strongly constrains achievable complexity, robustness, and duration of operation. | |||
Existing approaches to powering synthetic cells can be grouped into three broad classes, distinguished by where energy is generated and how it is coupled to the cellular load: | |||
* ''External feeding and renewal'' supplies ATP precursors, nucleotides, amino acids, and cofactors continuously from outside the synthetic cell via microfluidic exchange or permeable membranes. | |||
* ''Internal energy regeneration'' embeds enzymatic cascades, substrate-level phosphorylation pathways, or redox recycling systems within the synthetic cell to generate or recycle energy molecules in situ. | |||
* ''Membrane-coupled energy transduction'' reconstitutes proton pumps and ATP synthase in the synthetic cell membrane to convert light or chemical gradients into ATP, analogous to mitochondria or chloroplasts. | |||
The sections below describe each class in turn, followed by a discussion of how these approaches can be combined and regulated to meet the demands of a functioning synthetic cell. | |||
== External Feeding and Renewal == | |||
This section describes approaches in which energy substrates, nucleotides, and other consumables are supplied from outside the synthetic cell, either into open cell-free reaction mixtures or into encapsulated systems via permeable membranes or microfluidic exchange. | |||
=== Continuous External Feeding and Substrate Supply === | === Continuous External Feeding and Substrate Supply === | ||
One fundamental strategy involves continuously replenishing the synthetic cell's interior with fresh energy substrates and nutrients. In many cell‐free systems encapsulated in liposomes or giant unilamellar vesicles (GUVs), limited supply of substrates (e.g., ATP, nucleotides, amino acids) leads to eventual depletion that stops protein expression. To overcome this, external feeding protocols have been established such as microfluidic continuous exchange of reaction components. For example, microfluidic chemostats have been used to periodically replace part of the reaction volume with an energy solution that contains chemical substrates (e.g., creatine phosphate, nucleoside triphosphates) and replenishes lost amino acids and cofactors, thereby extending the time over which genetic circuits operate and proteins are synthesized <ref name="Lavickova2020"> | One fundamental strategy involves continuously replenishing the synthetic cell's interior with fresh energy substrates and nutrients. In many cell‐free systems encapsulated in liposomes or giant unilamellar vesicles (GUVs), limited supply of substrates (e.g., ATP, nucleotides, amino acids) leads to eventual depletion that stops protein expression. To overcome this, external feeding protocols have been established such as microfluidic continuous exchange of reaction components. For example, microfluidic chemostats have been used to periodically replace part of the reaction volume with an energy solution that contains chemical substrates (e.g., creatine phosphate, nucleoside triphosphates) and replenishes lost amino acids and cofactors, thereby extending the time over which genetic circuits operate and proteins are synthesized <ref name="Lavickova2020">B. Lavickova, N. Laohakunakorn, and S. J. Maerkl, [https://doi.org/10.1038/s41467-020-20180-6 A partially self-regenerating synthetic cell]. ''Nature Communications'' 11:6340, 2020. DOI: 10.1038/s41467-020-20180-6</ref>. In these systems, an external apparatus continuously feeds energy-rich substrates into synthetic compartments, offsetting the stoichiometric consumption that occurs during transcription and translation. This approach partially mimics the nutrient uptake and waste removal seen in living cells and is particularly useful in cell-free environments where metabolic regeneration is not intrinsic <ref name="Xu2016">C. Xu, S. Hu, and X. Chen, [https://doi.org/10.1016/j.mattod.2016.02.020 Artificial cells: from basic science to applications]. ''Materials Today'' 19(9):516–532, 2016. DOI: 10.1016/j.mattod.2016.02.020</ref>. | ||
=== Integration of Microfluidic Systems for Continuous Energy Renewal === | |||
Many synthetic cell platforms operate in a closed, batch-style environment, which limits the duration of protein expression because energy substrates are eventually depleted and inhibitory accumulations occur. Microfluidic platforms have been employed to overcome these limitations by creating a continuous exchange system, where fresh reaction solutions are fed into the synthetic cell environment at regular intervals <ref name="Lavickova2020" />. In these microfluidic chemostats, a portion of the reaction volume is periodically replaced with a nutrient-rich feed that contains all the necessary components for energy generation and gene expression. This approach not only sustains ATP levels but also buffers against waste accumulation, thereby extending the operational lifespan of the synthetic cells. The integration of such continuous-flow systems bridges the gap between static, closed-cell assays and the dynamic conditions that living cells experience, offering a promising route for long-term operation of artificial cells. | |||
=== Nucleotide Feeding and Waste Management === | |||
Beyond energy in the form of ATP, sustained operation of a synthetic cell requires a continuous supply of all four ribonucleoside triphosphates (NTPs: ATP, GTP, CTP, UTP) for transcription, as well as amino acids and other cofactors for translation. The PURE system, which reconstitutes cell-free transcription and translation from purified components, makes the full list of required inputs explicit<ref name="Shimizu2001">Y. Shimizu, A. Inoue, Y. Tomari, T. Suzuki, T. Yokogawa, K. Nishikawa, and T. Ueda, [https://doi.org/10.1038/90802 Cell-free translation reconstituted with purified components]. ''Nature Biotechnology'' 19:751–755, 2001. DOI: 10.1038/90802</ref>: in a closed batch system, all of these must be loaded at the start, and the system runs until whichever resource is first depleted. | |||
A particularly important waste product is inorganic phosphate (P<sub>i</sub>), the byproduct of NTP hydrolysis during transcription and translation. In a closed system, P<sub>i</sub> accumulates steadily over the course of a reaction and chelates free magnesium ions (Mg²⁺), which are an essential cofactor for ribosomes, RNA polymerase, and many other enzymes. The resulting drop in free Mg²⁺ concentration inhibits protein synthesis and can trigger ribosome degradation, and is a primary cause of the hours-long operational lifetime of batch cell-free systems<ref name="Jewett2004">M. C. Jewett and J. R. Swartz, [https://doi.org/10.1002/bit.20026 Mimicking the ''Escherichia coli'' cytoplasmic environment activates long-lived and efficient cell-free protein synthesis]. ''Biotechnology and Bioengineering'' 86(1):19–26, 2004. DOI: 10.1002/bit.20026</ref>. Strategies to mitigate phosphate accumulation include using phosphate-free energy sources such as pyruvate, which regenerates ATP without releasing inorganic phosphate as a net byproduct, and incorporating permeable membrane channels (such as α-hemolysin pores) or microfluidic exchange to allow continuous efflux of waste molecules into a surrounding buffer. | |||
More ambitious approaches aim to regenerate nucleotides and other consumables within the synthetic cell itself, rather than relying solely on external supply or dilution. Lavickova and colleagues demonstrated a partially self-regenerating synthetic cell in which key components of the transcription-translation machinery were replenished in situ, extending productive operation beyond what a simple batch system achieves<ref name="Lavickova2020" />. Achieving full nucleotide self-sufficiency remains an open challenge and is closely linked to progress on internal energy regeneration and membrane transport. | |||
== Internal Energy Regeneration == | |||
An alternative to external feeding is to embed the biochemical machinery for energy regeneration within the synthetic cell itself. The approaches described in this section generate or recycle ATP and cofactors in situ, using enzymatic cascades, substrate-level phosphorylation pathways, or redox recycling systems that operate inside the synthetic cell alongside the genetic circuits they power. | |||
=== Reconstituted ATP Regeneration Systems === | === Reconstituted ATP Regeneration Systems === | ||
Cell-free protein synthesis systems that traditionally rely on high-energy phosphate compounds such as phosphoenolpyruvate (PEP) or 3-phosphoglycerate (3-PGA) can be optimized by coupling with engineered metabolic enzymes to recycle phosphate and regenerate ATP <ref name="Gaut2021">Reconstituting Natural Cell Elements in Synthetic Cells. | Cell-free protein synthesis systems that traditionally rely on high-energy phosphate compounds such as phosphoenolpyruvate (PEP) or 3-phosphoglycerate (3-PGA) can be optimized by coupling with engineered metabolic enzymes to recycle phosphate and regenerate ATP <ref name="Gaut2021">N. J. Gaut and K. P. Adamala, [https://doi.org/10.1002/adbi.202000188 Reconstituting Natural Cell Elements in Synthetic Cells]. ''Advanced Biology'' (2021). DOI: 10.1002/adbi.202000188</ref>. These systems take advantage of enzymatic cascades in which one enzyme's product becomes the substrate for the next, effectively maintaining a pool of high-energy molecules to sustain protein synthesis. Although these methods can extend the duration of cell-free expression, challenges remain regarding phosphate bond instability and catalyst poisoning, which can lead to eventual cessation of activity. | ||
=== Enzymatic Cofactor and Metabolite Recycling === | === Enzymatic Cofactor and Metabolite Recycling === | ||
Efficient energy supply within synthetic cells not only depends on ATP regeneration but also on the reconstitution and continuous recycling of cofactors such as NADH and NADPH. Synthetic compartments have been developed that incorporate enzymatic cascades able to regenerate essential cofactors, thereby maintaining redox balance and sustaining metabolic reactions necessary for protein expression <ref name="Buddingh2017">Artificial Cells: Synthetic Compartments with Life-like Functionality and Adaptivity. | Efficient energy supply within synthetic cells not only depends on ATP regeneration but also on the reconstitution and continuous recycling of cofactors such as NADH and NADPH. Synthetic compartments have been developed that incorporate enzymatic cascades able to regenerate essential cofactors, thereby maintaining redox balance and sustaining metabolic reactions necessary for protein expression <ref name="Buddingh2017">B. C. Buddingh and J. C. M. van Hest, [https://doi.org/10.1021/acs.accounts.6b00512 Artificial Cells: Synthetic Compartments with Life-like Functionality and Adaptivity]. ''Accounts of Chemical Research'' (2017). DOI: 10.1021/acs.accounts.6b00512</ref>, <ref name="Otrin2019">L. Otrin, C. Kleineberg, L. Caire da Silva, K. Landfester, I. Ivanov, M. Wang, C. Bednarz, K. Sundmacher, and T. Vidaković‐Koch, [https://doi.org/10.1002/adbi.201800323 Artificial Organelles for Energy Regeneration]. ''Advanced Biosystems'' (2019). DOI: 10.1002/adbi.201800323</ref>. For instance, specific enzyme and electron donor systems have been demonstrated in polymersomes to continuously recycle NADPH, which in turn supports downstream biosynthetic reactions and energizes genetic circuits. These enzymatic recycling modules help sustain the out-of-equilibrium conditions required for extended operation of synthetic biological processes. | ||
=== Metabolic Pathway Engineering and Substrate-Level Phosphorylation === | |||
Beyond the reconstitution of classical energy modules involving ATP synthase, synthetic cells have been designed to include minimal metabolic pathways that directly generate ATP through substrate-level phosphorylation. One example is the arginine breakdown pathway, which has been reconstituted in liposomes to drive ATP production from energy-rich substrates <ref name="Sikkema2019">H. R. Sikkema, B. F. Gaastra, T. Pols, and B. Poolman, [https://doi.org/10.1002/cbic.201900398 Cell Fuelling and Metabolic Energy Conservation in Synthetic Cells]. ''ChemBioChem'' (2019). DOI: 10.1002/cbic.201900398</ref>. In such systems, the conversion of arginine to ornithine is coupled to ATP generation via carbamate kinase, and the process is facilitated by membrane transporters that exchange substrates and products. These pathways, although simpler than full respiratory chains, can provide a bona fide ATP supply to support energetically demanding processes such as translation and genetic circuit operation <ref name="Sikkema2019" />. By designing these pathways carefully, researchers can mimic the efficiency of natural mitochondrial ATP production in a much more simplified and controlled environment. | |||
=== Integration | === Integration with Native or Engineered Metabolic Systems === | ||
In some approaches, synthetic cells are designed to incorporate elements of natural metabolism, borrowing components from living cells to jumpstart robust energy production. For example, cell-free protein synthesis systems that reconstitute elements of the E. coli cytoplasm have been used to support long-term protein production. Such systems include not only the biochemical machinery for transcription and translation but also enzymes for ATP and cofactor regeneration <ref name="Gaut2021" />, <ref name="Buddingh2017" />. By adopting metabolic modules from natural organisms, synthetic cell designs can leverage billions of years of evolutionary optimization to maintain high energetic efficiency and resilience against metabolic imbalance. | |||
== | == Membrane-Coupled Energy Transduction == | ||
For use in synthetic cells, the energy regeneration and waste processing systems must operate in an encapsulated environment. | For use in synthetic cells, the energy regeneration and waste processing systems must operate in an encapsulated environment. Several approaches have been explored in the literature. | ||
=== Integration of Artificial Organelles === | === Integration of Artificial Organelles === | ||
Another promising approach is the design of modular artificial organelles—compartmentalized subunits embedded within synthetic cells that mimic the energy conversion functions of mitochondria or chloroplasts. Such artificial organelles typically integrate a photoconverter (e.g., bacteriorhodopsin or photosystem II), an ATP synthase, and a compartment that maintains the proton motive force | Another promising approach is the design of modular artificial organelles—compartmentalized subunits embedded within synthetic cells that mimic the energy conversion functions of mitochondria or chloroplasts. Such artificial organelles typically integrate a photoconverter (e.g., bacteriorhodopsin or photosystem II), an ATP synthase, and a compartment that maintains the proton motive force <ref name="Otrin2019" />. By partitioning the energy-generating reactions into discrete subcompartments, synthetic cells can achieve spatial organization similar to eukaryotic cells, which in turn helps protect sensitive reactions from interference and allows for regulated energy supply. These enzyme-coupled systems have been further optimized by modulating the membrane composition and protein orientation to maximize the efficiency of ATP synthesis and reduce leakiness <ref name="Buddingh2017" />. | ||
=== Light-Driven Energy Systems === | === Light-Driven Energy Systems === | ||
A common goal is to establish internal modules within synthetic cells that can cyclically regenerate ATP, the universal energy currency. One successful approach has been to incorporate membrane-bound ATP synthase together with proton pumps into vesicles, thereby recreating a minimal version of natural bioenergetics. Light-driven systems are a prominent example. In such systems, proteins such as bacteriorhodopsin or proteorhodopsin are co-reconstituted with ATP synthase in lipid bilayers or polymersomes; upon illumination, the light-sensitive proton pump establishes a proton gradient across the membrane, which the ATP synthase then harnesses to convert ADP into ATP <ref name="Jeong2020">Toward Artificial Cells: Novel Advances in Energy Conversion and Cellular Motility. | A common goal is to establish internal modules within synthetic cells that can cyclically regenerate ATP, the universal energy currency. One successful approach has been to incorporate membrane-bound ATP synthase together with proton pumps into vesicles, thereby recreating a minimal version of natural bioenergetics. Light-driven systems are a prominent example. In such systems, proteins such as bacteriorhodopsin or proteorhodopsin are co-reconstituted with ATP synthase in lipid bilayers or polymersomes; upon illumination, the light-sensitive proton pump establishes a proton gradient across the membrane, which the ATP synthase then harnesses to convert ADP into ATP <ref name="Jeong2020">S. Jeong, H. T. Nguyen, C. H. Kim, M. N. Ly, and K. Shin, [https://doi.org/10.1002/adfm.201907182 Toward Artificial Cells: Novel Advances in Energy Conversion and Cellular Motility]. ''Advanced Functional Materials'' (2020). DOI: 10.1002/adfm.201907182</ref>, <ref name="Otrin2019" />. This strategy has been validated by early work showing that light-induced proton gradients can drive ATP production, drawing analogies to natural photosynthesis, and it is now under active refinement to achieve higher synthesis rates and longer operation times <ref name="Berhanu2019">S. Berhanu, T. Ueda, and Y. Kuruma, [https://doi.org/10.1038/s41467-019-09147-4 Artificial photosynthetic cell producing energy for protein synthesis]. ''Nature Communications'' (2019). DOI: 10.1038/s41467-019-09147-4</ref>, <ref name="Schwille2018">P. Schwille, J. Spatz, K. Landfester, E. Bodenschatz, S. Herminghaus, V. Sourjik, T. J. Erb, P. Bastiaens, R. Lipowsky, A. Hyman, P. Dabrock, J.-C. Baret, T. Vidakovic‐Koch, P. Bieling, R. Dimova, H. Mutschler, T. Robinson, T.-Y. D. Tang, S. Wegner, and K. Sundmacher, [https://doi.org/10.1002/anie.201802288 MaxSynBio: Avenues Towards Creating Cells from the Bottom Up]. ''Angewandte Chemie International Edition'' (2018). DOI: 10.1002/anie.201802288</ref>. | ||
Light-driven energy generation stands out as one of the most attractive strategies for powering synthetic cells, primarily because it allows for energy input in a renewable and externally controllable manner. The reconstitution of light-activated proton pumps such as bacteriorhodopsin (or its variants) in combination with ATP synthase enables synthetic cells to utilize light as a free energy source. Not only is this strategy renewable, but it also allows for precise external control over energy production, which is advantageous in systems where timing and spatial regulation of genetic circuits are crucial. | Light-driven energy generation stands out as one of the most attractive strategies for powering synthetic cells, primarily because it allows for energy input in a renewable and externally controllable manner. The reconstitution of light-activated proton pumps such as bacteriorhodopsin (or its variants) in combination with ATP synthase enables synthetic cells to utilize light as a free energy source. Not only is this strategy renewable, but it also allows for precise external control over energy production, which is advantageous in systems where timing and spatial regulation of genetic circuits are crucial. | ||
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Another necessary element for long-term operation is ensuring that the synthetic cell membrane can both retain key biomacromolecules while allowing the controlled exchange of small energy substrates and waste products. Several approaches have been developed to modify vesicle permeability. One effective strategy is the incorporation of pore-forming proteins such as α-hemolysin into liposomal membranes, thereby permitting passive diffusion of small molecules including nutrients, ATP, and cofactors <ref name="Xu2016" />, <ref name="Jeong2020" />. The presence of these pores allows for a continuous supply of vital substrates and removal of inhibitory products from within the synthetic cell, enabling sustained protein expression and circuit operation. Importantly, the selective permeability of these membranes can be engineered by tuning the composition of lipid mixtures to favor the necessary pore formation while maintaining compartment integrity <ref name="Buddingh2017" />. | Another necessary element for long-term operation is ensuring that the synthetic cell membrane can both retain key biomacromolecules while allowing the controlled exchange of small energy substrates and waste products. Several approaches have been developed to modify vesicle permeability. One effective strategy is the incorporation of pore-forming proteins such as α-hemolysin into liposomal membranes, thereby permitting passive diffusion of small molecules including nutrients, ATP, and cofactors <ref name="Xu2016" />, <ref name="Jeong2020" />. The presence of these pores allows for a continuous supply of vital substrates and removal of inhibitory products from within the synthetic cell, enabling sustained protein expression and circuit operation. Importantly, the selective permeability of these membranes can be engineered by tuning the composition of lipid mixtures to favor the necessary pore formation while maintaining compartment integrity <ref name="Buddingh2017" />. | ||
=== Use of Synthetic Membrane Materials and Compartmentalization Strategies === | === Use of Synthetic Membrane Materials and Compartmentalization Strategies === | ||
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The choice of membrane material is critical not only for providing structural integrity but also for functional support of embedded energy-conversion modules. Synthetic cells have been constructed using lipid vesicles, polymersomes, or hybrid membranes that can be tailored to optimize both permeability and stability <ref name="Buddingh2017" />, <ref name="Xu2016" />. Hybrid membranes, particularly those incorporating block-copolymers with phospholipids, offer enhanced stability and controlled permeability, which is necessary when integrating sensitive proteins such as ATP synthase and proton pumps. In addition, compartmentalization via the creation of internal subcompartments (artificial organelles) enables spatial separation of incompatible reactions while concentrating key enzymes and substrates. This design mimics the organelle organization found in natural eukaryotic cells and facilitates higher local concentrations of metabolic components, thereby increasing ATP synthesis efficiency <ref name="Gaut2021" />, <ref name="Otrin2019" />. | The choice of membrane material is critical not only for providing structural integrity but also for functional support of embedded energy-conversion modules. Synthetic cells have been constructed using lipid vesicles, polymersomes, or hybrid membranes that can be tailored to optimize both permeability and stability <ref name="Buddingh2017" />, <ref name="Xu2016" />. Hybrid membranes, particularly those incorporating block-copolymers with phospholipids, offer enhanced stability and controlled permeability, which is necessary when integrating sensitive proteins such as ATP synthase and proton pumps. In addition, compartmentalization via the creation of internal subcompartments (artificial organelles) enables spatial separation of incompatible reactions while concentrating key enzymes and substrates. This design mimics the organelle organization found in natural eukaryotic cells and facilitates higher local concentrations of metabolic components, thereby increasing ATP synthesis efficiency <ref name="Gaut2021" />, <ref name="Otrin2019" />. | ||
== | == Metabolism as a Regulated Subsystem == | ||
Across all three classes, a common engineering challenge is matching energy generation to time-varying demand while maintaining internal homeostasis. For synthetic cells, this suggests treating the metabolic subsystem not as a static background process but as a regulated module with defined input–output characteristics — analogous to a power supply with a feedback-controlled output. Key open challenges include: | |||
* ''Energy sensing and feedback'': integrating sensors that monitor intracellular ATP levels, pH, or redox state and trigger compensatory responses when energy availability falls below threshold. Genetically encoded or chemically based sensors can provide real-time information and couple to feedback loops that adjust substrate uptake or enzyme activity. | |||
* ''Waste management'': inhibitory byproducts (inorganic phosphate, ADP, oxidized cofactors) accumulate in closed systems and progressively degrade performance. Strategies include permeable membranes for passive efflux, enzymatic scavenging pathways, and microfluidic exchange. | |||
* ''Standardized interfaces'': defining the energy output characteristics of a metabolic module (e.g., steady-state ATP concentration, regeneration rate, load tolerance) in a way that allows it to be composed with sensing, computation, and actuation subsystems developed independently. This is essential for the modular assembly of synthetic cells from interoperable components. | |||
Progress on these fronts is essential for extending operational lifetime and for realizing the vision of synthetic cells as interoperable, stackable building blocks. | |||
== Future Perspectives and Remaining Challenges == | == Future Perspectives and Remaining Challenges == | ||
Although significant progress has been made, several challenges remain in fully realizing autonomous energy supply within synthetic cells. One key challenge is matching the efficiency and dynamic range of natural metabolic networks. For long-term operation, the synthetic energy modules must not only produce sufficient ATP at high rates but also recycle all necessary cofactors and remove inhibitory byproducts. Ensuring membrane integrity while embedding multiple active proteins also remains a technical hurdle, as does the precise calibration of substrate and enzyme concentrations to avoid imbalances that could shut down energy production <ref name="Sikkema2019" / | Although significant progress has been made, several challenges remain in fully realizing autonomous energy supply within synthetic cells. One key challenge is matching the efficiency and dynamic range of natural metabolic networks. For long-term operation, the synthetic energy modules must not only produce sufficient ATP at high rates but also recycle all necessary cofactors and remove inhibitory byproducts. Ensuring membrane integrity while embedding multiple active proteins also remains a technical hurdle, as does the precise calibration of substrate and enzyme concentrations to avoid imbalances that could shut down energy production <ref name="Sikkema2019" />. | ||
Furthermore, while continuous feeding through microfluidic systems has shown promise in maintaining steady-state conditions, integration of such systems into fully autonomous or implantable synthetic cells is still in its infancy <ref name="Lavickova2020 | Furthermore, while continuous feeding through microfluidic systems has shown promise in maintaining steady-state conditions, integration of such systems into fully autonomous or implantable synthetic cells is still in its infancy <ref name="Lavickova2020" />. The eventual goal is to develop synthetic cells that are capable of self-sustained energy production over long periods without the need for external intervention—a milestone that will require further optimization of membrane materials, metabolic pathway integration, and feedback control mechanisms <ref name="Sikkema2019" />, <ref name="Xu2016" />. | ||
Consequently, continued research in reconstituting natural energy-converting enzyme complexes, designing modular artificial organelles, and optimizing microfluidic continuous replacement strategies is essential. Advances in synthetic biology techniques, combined with insights from natural cellular bioenergetics, will undoubtedly propel the field closer to creating fully autonomous synthetic cells. Future designs may also integrate environmentally responsive elements that allow synthetic cells to adaptively alter their energy regimes in response to changing external conditions <ref name="Gaut2021" />, <ref name="Schwille2018" />. | Consequently, continued research in reconstituting natural energy-converting enzyme complexes, designing modular artificial organelles, and optimizing microfluidic continuous replacement strategies is essential. Advances in synthetic biology techniques, combined with insights from natural cellular bioenergetics, will undoubtedly propel the field closer to creating fully autonomous synthetic cells. Future designs may also integrate environmentally responsive elements that allow synthetic cells to adaptively alter their energy regimes in response to changing external conditions <ref name="Gaut2021" />, <ref name="Schwille2018" />. | ||
In summary, the current approaches to supplying synthetic cells with energy include: continuous external supply of energy substrates via microfluidic feeding, reconstitution of ATP regeneration systems that harness light-driven or chemical energy, enzymatic recycling of cofactors such as NADPH and NADH, incorporation of artificial organelles that mimic natural bioenergetic organelles, and the development of membranes with tunable permeability to allow selective nutrient influx and waste efflux. These strategies are often combined in hybrid systems to maximize energy production efficiency, improve robustness, and enable extended operation of genetic circuits and protein expression. Advances in material science, enzyme reconstitution, and system integration are critical to overcoming current limitations and achieving self-sustaining synthetic cells that can operate for prolonged periods with minimal external intervention <ref name="Buddingh2017" />, <ref name="Jeong2020" />, <ref name="Otrin2019" />, <ref name="Sikkema2019" / | In summary, the current approaches to supplying synthetic cells with energy include: continuous external supply of energy substrates via microfluidic feeding, reconstitution of ATP regeneration systems that harness light-driven or chemical energy, enzymatic recycling of cofactors such as NADPH and NADH, incorporation of artificial organelles that mimic natural bioenergetic organelles, and the development of membranes with tunable permeability to allow selective nutrient influx and waste efflux. These strategies are often combined in hybrid systems to maximize energy production efficiency, improve robustness, and enable extended operation of genetic circuits and protein expression. Advances in material science, enzyme reconstitution, and system integration are critical to overcoming current limitations and achieving self-sustaining synthetic cells that can operate for prolonged periods with minimal external intervention <ref name="Buddingh2017" />, <ref name="Jeong2020" />, <ref name="Otrin2019" />, <ref name="Sikkema2019" />. | ||
This multi-pronged approach to energy supply is essential not only for sustaining protein synthesis and gene expression but also for enabling more complex cell-like behaviors such as growth, division, and response to environmental cues. As researchers continue to refine these techniques, the integration of energy regeneration modules will remain one of the central challenges and opportunities for the field of artificial cells. | This multi-pronged approach to energy supply is essential not only for sustaining protein synthesis and gene expression but also for enabling more complex cell-like behaviors such as growth, division, and response to environmental cues. As researchers continue to refine these techniques, the integration of energy regeneration modules will remain one of the central challenges and opportunities for the field of artificial cells. | ||
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Overall, the field has evolved from relying on simple, batch-fed cell-free protein expression systems to developing sophisticated, compartmentalized energy regeneration strategies that recapitulate natural metabolic and bioenergetic processes. This progress paves the way for the development of synthetic cells that can autonomously sustain complex genetic circuits and perform prolonged, life-like functions in both in vitro settings and, eventually, in vivo applications <ref name="Gaut2021" />, <ref name="Buddingh2017" />, <ref name="Xu2016" />. | Overall, the field has evolved from relying on simple, batch-fed cell-free protein expression systems to developing sophisticated, compartmentalized energy regeneration strategies that recapitulate natural metabolic and bioenergetic processes. This progress paves the way for the development of synthetic cells that can autonomously sustain complex genetic circuits and perform prolonged, life-like functions in both in vitro settings and, eventually, in vivo applications <ref name="Gaut2021" />, <ref name="Buddingh2017" />, <ref name="Xu2016" />. | ||
By combining continuous nutrient supply, in situ ATP and cofactor regeneration, selective membrane permeability via channel proteins, and integration of artificial organelles, researchers are steadily advancing toward the creation of a fully autonomous synthetic cell with robust energy management. Future research will need to address remaining challenges such as protein insertion efficiency, control of reaction byproducts, and fine-tuning biophysical properties of synthetic membranes to further bridge the gap between engineered systems and natural cells | By combining continuous nutrient supply, in situ ATP and cofactor regeneration, selective membrane permeability via channel proteins, and integration of artificial organelles, researchers are steadily advancing toward the creation of a fully autonomous synthetic cell with robust energy management. Future research will need to address remaining challenges such as protein insertion efficiency, control of reaction byproducts, and fine-tuning biophysical properties of synthetic membranes to further bridge the gap between engineered systems and natural cells <ref name="Sikkema2019" />. | ||
The cumulative progress in these areas represents a significant step forward in synthetic biology and brings us closer to the ultimate goal of constructing artificial cells that are capable of sustained, self-regulated operation, thereby providing a viable platform for applications ranging from drug delivery to biosensing and beyond <ref name="Jeong2020 | The cumulative progress in these areas represents a significant step forward in synthetic biology and brings us closer to the ultimate goal of constructing artificial cells that are capable of sustained, self-regulated operation, thereby providing a viable platform for applications ranging from drug delivery to biosensing and beyond <ref name="Jeong2020" />. | ||
== References == | == References == | ||
Latest revision as of 06:16, 27 June 2026
This page was originally generated using the FutureHouse Falcon deep search tool in response to the following query: "What are the various ways in which synthetic cells (also called artificial cells) can be supplied with energy, to allow operation of genetic circuits and/or protein expression to be carried out for longer period of time." The text was then rearranged and edited to provide more structure and context. The page was further modified based on the paper Engineering Biology at Scale Using Synthetic Cells: A Systems and Control Perspective (Murray, 2026), using Claude Code to assist with integration and formatting. This page was reviewed by the author on 27 Jun 2026.
Overview
The metabolic subsystem provides the energy required for a synthetic cell to operate. Even modest genetic circuits and actuation modules can rapidly exhaust the energy resources available in a closed cell-free system, causing shutdown on the timescale of hours[1]. As a result, energy supply should be viewed not as an auxiliary concern but as a core enabling service whose design strongly constrains achievable complexity, robustness, and duration of operation.
Existing approaches to powering synthetic cells can be grouped into three broad classes, distinguished by where energy is generated and how it is coupled to the cellular load:
- External feeding and renewal supplies ATP precursors, nucleotides, amino acids, and cofactors continuously from outside the synthetic cell via microfluidic exchange or permeable membranes.
- Internal energy regeneration embeds enzymatic cascades, substrate-level phosphorylation pathways, or redox recycling systems within the synthetic cell to generate or recycle energy molecules in situ.
- Membrane-coupled energy transduction reconstitutes proton pumps and ATP synthase in the synthetic cell membrane to convert light or chemical gradients into ATP, analogous to mitochondria or chloroplasts.
The sections below describe each class in turn, followed by a discussion of how these approaches can be combined and regulated to meet the demands of a functioning synthetic cell.
External Feeding and Renewal
This section describes approaches in which energy substrates, nucleotides, and other consumables are supplied from outside the synthetic cell, either into open cell-free reaction mixtures or into encapsulated systems via permeable membranes or microfluidic exchange.
Continuous External Feeding and Substrate Supply
One fundamental strategy involves continuously replenishing the synthetic cell's interior with fresh energy substrates and nutrients. In many cell‐free systems encapsulated in liposomes or giant unilamellar vesicles (GUVs), limited supply of substrates (e.g., ATP, nucleotides, amino acids) leads to eventual depletion that stops protein expression. To overcome this, external feeding protocols have been established such as microfluidic continuous exchange of reaction components. For example, microfluidic chemostats have been used to periodically replace part of the reaction volume with an energy solution that contains chemical substrates (e.g., creatine phosphate, nucleoside triphosphates) and replenishes lost amino acids and cofactors, thereby extending the time over which genetic circuits operate and proteins are synthesized [2]. In these systems, an external apparatus continuously feeds energy-rich substrates into synthetic compartments, offsetting the stoichiometric consumption that occurs during transcription and translation. This approach partially mimics the nutrient uptake and waste removal seen in living cells and is particularly useful in cell-free environments where metabolic regeneration is not intrinsic [3].
Integration of Microfluidic Systems for Continuous Energy Renewal
Many synthetic cell platforms operate in a closed, batch-style environment, which limits the duration of protein expression because energy substrates are eventually depleted and inhibitory accumulations occur. Microfluidic platforms have been employed to overcome these limitations by creating a continuous exchange system, where fresh reaction solutions are fed into the synthetic cell environment at regular intervals [2]. In these microfluidic chemostats, a portion of the reaction volume is periodically replaced with a nutrient-rich feed that contains all the necessary components for energy generation and gene expression. This approach not only sustains ATP levels but also buffers against waste accumulation, thereby extending the operational lifespan of the synthetic cells. The integration of such continuous-flow systems bridges the gap between static, closed-cell assays and the dynamic conditions that living cells experience, offering a promising route for long-term operation of artificial cells.
Nucleotide Feeding and Waste Management
Beyond energy in the form of ATP, sustained operation of a synthetic cell requires a continuous supply of all four ribonucleoside triphosphates (NTPs: ATP, GTP, CTP, UTP) for transcription, as well as amino acids and other cofactors for translation. The PURE system, which reconstitutes cell-free transcription and translation from purified components, makes the full list of required inputs explicit[4]: in a closed batch system, all of these must be loaded at the start, and the system runs until whichever resource is first depleted.
A particularly important waste product is inorganic phosphate (Pi), the byproduct of NTP hydrolysis during transcription and translation. In a closed system, Pi accumulates steadily over the course of a reaction and chelates free magnesium ions (Mg²⁺), which are an essential cofactor for ribosomes, RNA polymerase, and many other enzymes. The resulting drop in free Mg²⁺ concentration inhibits protein synthesis and can trigger ribosome degradation, and is a primary cause of the hours-long operational lifetime of batch cell-free systems[1]. Strategies to mitigate phosphate accumulation include using phosphate-free energy sources such as pyruvate, which regenerates ATP without releasing inorganic phosphate as a net byproduct, and incorporating permeable membrane channels (such as α-hemolysin pores) or microfluidic exchange to allow continuous efflux of waste molecules into a surrounding buffer.
More ambitious approaches aim to regenerate nucleotides and other consumables within the synthetic cell itself, rather than relying solely on external supply or dilution. Lavickova and colleagues demonstrated a partially self-regenerating synthetic cell in which key components of the transcription-translation machinery were replenished in situ, extending productive operation beyond what a simple batch system achieves[2]. Achieving full nucleotide self-sufficiency remains an open challenge and is closely linked to progress on internal energy regeneration and membrane transport.
Internal Energy Regeneration
An alternative to external feeding is to embed the biochemical machinery for energy regeneration within the synthetic cell itself. The approaches described in this section generate or recycle ATP and cofactors in situ, using enzymatic cascades, substrate-level phosphorylation pathways, or redox recycling systems that operate inside the synthetic cell alongside the genetic circuits they power.
Reconstituted ATP Regeneration Systems
Cell-free protein synthesis systems that traditionally rely on high-energy phosphate compounds such as phosphoenolpyruvate (PEP) or 3-phosphoglycerate (3-PGA) can be optimized by coupling with engineered metabolic enzymes to recycle phosphate and regenerate ATP [5]. These systems take advantage of enzymatic cascades in which one enzyme's product becomes the substrate for the next, effectively maintaining a pool of high-energy molecules to sustain protein synthesis. Although these methods can extend the duration of cell-free expression, challenges remain regarding phosphate bond instability and catalyst poisoning, which can lead to eventual cessation of activity.
Enzymatic Cofactor and Metabolite Recycling
Efficient energy supply within synthetic cells not only depends on ATP regeneration but also on the reconstitution and continuous recycling of cofactors such as NADH and NADPH. Synthetic compartments have been developed that incorporate enzymatic cascades able to regenerate essential cofactors, thereby maintaining redox balance and sustaining metabolic reactions necessary for protein expression [6], [7]. For instance, specific enzyme and electron donor systems have been demonstrated in polymersomes to continuously recycle NADPH, which in turn supports downstream biosynthetic reactions and energizes genetic circuits. These enzymatic recycling modules help sustain the out-of-equilibrium conditions required for extended operation of synthetic biological processes.
Metabolic Pathway Engineering and Substrate-Level Phosphorylation
Beyond the reconstitution of classical energy modules involving ATP synthase, synthetic cells have been designed to include minimal metabolic pathways that directly generate ATP through substrate-level phosphorylation. One example is the arginine breakdown pathway, which has been reconstituted in liposomes to drive ATP production from energy-rich substrates [8]. In such systems, the conversion of arginine to ornithine is coupled to ATP generation via carbamate kinase, and the process is facilitated by membrane transporters that exchange substrates and products. These pathways, although simpler than full respiratory chains, can provide a bona fide ATP supply to support energetically demanding processes such as translation and genetic circuit operation [8]. By designing these pathways carefully, researchers can mimic the efficiency of natural mitochondrial ATP production in a much more simplified and controlled environment.
Integration with Native or Engineered Metabolic Systems
In some approaches, synthetic cells are designed to incorporate elements of natural metabolism, borrowing components from living cells to jumpstart robust energy production. For example, cell-free protein synthesis systems that reconstitute elements of the E. coli cytoplasm have been used to support long-term protein production. Such systems include not only the biochemical machinery for transcription and translation but also enzymes for ATP and cofactor regeneration [5], [6]. By adopting metabolic modules from natural organisms, synthetic cell designs can leverage billions of years of evolutionary optimization to maintain high energetic efficiency and resilience against metabolic imbalance.
Membrane-Coupled Energy Transduction
For use in synthetic cells, the energy regeneration and waste processing systems must operate in an encapsulated environment. Several approaches have been explored in the literature.
Integration of Artificial Organelles
Another promising approach is the design of modular artificial organelles—compartmentalized subunits embedded within synthetic cells that mimic the energy conversion functions of mitochondria or chloroplasts. Such artificial organelles typically integrate a photoconverter (e.g., bacteriorhodopsin or photosystem II), an ATP synthase, and a compartment that maintains the proton motive force [7]. By partitioning the energy-generating reactions into discrete subcompartments, synthetic cells can achieve spatial organization similar to eukaryotic cells, which in turn helps protect sensitive reactions from interference and allows for regulated energy supply. These enzyme-coupled systems have been further optimized by modulating the membrane composition and protein orientation to maximize the efficiency of ATP synthesis and reduce leakiness [6].
Light-Driven Energy Systems
A common goal is to establish internal modules within synthetic cells that can cyclically regenerate ATP, the universal energy currency. One successful approach has been to incorporate membrane-bound ATP synthase together with proton pumps into vesicles, thereby recreating a minimal version of natural bioenergetics. Light-driven systems are a prominent example. In such systems, proteins such as bacteriorhodopsin or proteorhodopsin are co-reconstituted with ATP synthase in lipid bilayers or polymersomes; upon illumination, the light-sensitive proton pump establishes a proton gradient across the membrane, which the ATP synthase then harnesses to convert ADP into ATP [9], [7]. This strategy has been validated by early work showing that light-induced proton gradients can drive ATP production, drawing analogies to natural photosynthesis, and it is now under active refinement to achieve higher synthesis rates and longer operation times [10], [11].
Light-driven energy generation stands out as one of the most attractive strategies for powering synthetic cells, primarily because it allows for energy input in a renewable and externally controllable manner. The reconstitution of light-activated proton pumps such as bacteriorhodopsin (or its variants) in combination with ATP synthase enables synthetic cells to utilize light as a free energy source. Not only is this strategy renewable, but it also allows for precise external control over energy production, which is advantageous in systems where timing and spatial regulation of genetic circuits are crucial.
Membrane Permeabilization and Nutrient Uptake
Another necessary element for long-term operation is ensuring that the synthetic cell membrane can both retain key biomacromolecules while allowing the controlled exchange of small energy substrates and waste products. Several approaches have been developed to modify vesicle permeability. One effective strategy is the incorporation of pore-forming proteins such as α-hemolysin into liposomal membranes, thereby permitting passive diffusion of small molecules including nutrients, ATP, and cofactors [3], [9]. The presence of these pores allows for a continuous supply of vital substrates and removal of inhibitory products from within the synthetic cell, enabling sustained protein expression and circuit operation. Importantly, the selective permeability of these membranes can be engineered by tuning the composition of lipid mixtures to favor the necessary pore formation while maintaining compartment integrity [6].
Use of Synthetic Membrane Materials and Compartmentalization Strategies
The choice of membrane material is critical not only for providing structural integrity but also for functional support of embedded energy-conversion modules. Synthetic cells have been constructed using lipid vesicles, polymersomes, or hybrid membranes that can be tailored to optimize both permeability and stability [6], [3]. Hybrid membranes, particularly those incorporating block-copolymers with phospholipids, offer enhanced stability and controlled permeability, which is necessary when integrating sensitive proteins such as ATP synthase and proton pumps. In addition, compartmentalization via the creation of internal subcompartments (artificial organelles) enables spatial separation of incompatible reactions while concentrating key enzymes and substrates. This design mimics the organelle organization found in natural eukaryotic cells and facilitates higher local concentrations of metabolic components, thereby increasing ATP synthesis efficiency [5], [7].
Metabolism as a Regulated Subsystem
Across all three classes, a common engineering challenge is matching energy generation to time-varying demand while maintaining internal homeostasis. For synthetic cells, this suggests treating the metabolic subsystem not as a static background process but as a regulated module with defined input–output characteristics — analogous to a power supply with a feedback-controlled output. Key open challenges include:
- Energy sensing and feedback: integrating sensors that monitor intracellular ATP levels, pH, or redox state and trigger compensatory responses when energy availability falls below threshold. Genetically encoded or chemically based sensors can provide real-time information and couple to feedback loops that adjust substrate uptake or enzyme activity.
- Waste management: inhibitory byproducts (inorganic phosphate, ADP, oxidized cofactors) accumulate in closed systems and progressively degrade performance. Strategies include permeable membranes for passive efflux, enzymatic scavenging pathways, and microfluidic exchange.
- Standardized interfaces: defining the energy output characteristics of a metabolic module (e.g., steady-state ATP concentration, regeneration rate, load tolerance) in a way that allows it to be composed with sensing, computation, and actuation subsystems developed independently. This is essential for the modular assembly of synthetic cells from interoperable components.
Progress on these fronts is essential for extending operational lifetime and for realizing the vision of synthetic cells as interoperable, stackable building blocks.
Future Perspectives and Remaining Challenges
Although significant progress has been made, several challenges remain in fully realizing autonomous energy supply within synthetic cells. One key challenge is matching the efficiency and dynamic range of natural metabolic networks. For long-term operation, the synthetic energy modules must not only produce sufficient ATP at high rates but also recycle all necessary cofactors and remove inhibitory byproducts. Ensuring membrane integrity while embedding multiple active proteins also remains a technical hurdle, as does the precise calibration of substrate and enzyme concentrations to avoid imbalances that could shut down energy production [8].
Furthermore, while continuous feeding through microfluidic systems has shown promise in maintaining steady-state conditions, integration of such systems into fully autonomous or implantable synthetic cells is still in its infancy [2]. The eventual goal is to develop synthetic cells that are capable of self-sustained energy production over long periods without the need for external intervention—a milestone that will require further optimization of membrane materials, metabolic pathway integration, and feedback control mechanisms [8], [3].
Consequently, continued research in reconstituting natural energy-converting enzyme complexes, designing modular artificial organelles, and optimizing microfluidic continuous replacement strategies is essential. Advances in synthetic biology techniques, combined with insights from natural cellular bioenergetics, will undoubtedly propel the field closer to creating fully autonomous synthetic cells. Future designs may also integrate environmentally responsive elements that allow synthetic cells to adaptively alter their energy regimes in response to changing external conditions [5], [11].
In summary, the current approaches to supplying synthetic cells with energy include: continuous external supply of energy substrates via microfluidic feeding, reconstitution of ATP regeneration systems that harness light-driven or chemical energy, enzymatic recycling of cofactors such as NADPH and NADH, incorporation of artificial organelles that mimic natural bioenergetic organelles, and the development of membranes with tunable permeability to allow selective nutrient influx and waste efflux. These strategies are often combined in hybrid systems to maximize energy production efficiency, improve robustness, and enable extended operation of genetic circuits and protein expression. Advances in material science, enzyme reconstitution, and system integration are critical to overcoming current limitations and achieving self-sustaining synthetic cells that can operate for prolonged periods with minimal external intervention [6], [9], [7], [8].
This multi-pronged approach to energy supply is essential not only for sustaining protein synthesis and gene expression but also for enabling more complex cell-like behaviors such as growth, division, and response to environmental cues. As researchers continue to refine these techniques, the integration of energy regeneration modules will remain one of the central challenges and opportunities for the field of artificial cells.
Overall, the field has evolved from relying on simple, batch-fed cell-free protein expression systems to developing sophisticated, compartmentalized energy regeneration strategies that recapitulate natural metabolic and bioenergetic processes. This progress paves the way for the development of synthetic cells that can autonomously sustain complex genetic circuits and perform prolonged, life-like functions in both in vitro settings and, eventually, in vivo applications [5], [6], [3].
By combining continuous nutrient supply, in situ ATP and cofactor regeneration, selective membrane permeability via channel proteins, and integration of artificial organelles, researchers are steadily advancing toward the creation of a fully autonomous synthetic cell with robust energy management. Future research will need to address remaining challenges such as protein insertion efficiency, control of reaction byproducts, and fine-tuning biophysical properties of synthetic membranes to further bridge the gap between engineered systems and natural cells [8].
The cumulative progress in these areas represents a significant step forward in synthetic biology and brings us closer to the ultimate goal of constructing artificial cells that are capable of sustained, self-regulated operation, thereby providing a viable platform for applications ranging from drug delivery to biosensing and beyond [9].
References
- ↑ 1.0 1.1 M. C. Jewett and J. R. Swartz, Mimicking the Escherichia coli cytoplasmic environment activates long-lived and efficient cell-free protein synthesis. Biotechnology and Bioengineering 86(1):19–26, 2004. DOI: 10.1002/bit.20026
- ↑ 2.0 2.1 2.2 2.3 B. Lavickova, N. Laohakunakorn, and S. J. Maerkl, A partially self-regenerating synthetic cell. Nature Communications 11:6340, 2020. DOI: 10.1038/s41467-020-20180-6
- ↑ 3.0 3.1 3.2 3.3 3.4 C. Xu, S. Hu, and X. Chen, Artificial cells: from basic science to applications. Materials Today 19(9):516–532, 2016. DOI: 10.1016/j.mattod.2016.02.020
- ↑ Y. Shimizu, A. Inoue, Y. Tomari, T. Suzuki, T. Yokogawa, K. Nishikawa, and T. Ueda, Cell-free translation reconstituted with purified components. Nature Biotechnology 19:751–755, 2001. DOI: 10.1038/90802
- ↑ 5.0 5.1 5.2 5.3 5.4 N. J. Gaut and K. P. Adamala, Reconstituting Natural Cell Elements in Synthetic Cells. Advanced Biology (2021). DOI: 10.1002/adbi.202000188
- ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 B. C. Buddingh and J. C. M. van Hest, Artificial Cells: Synthetic Compartments with Life-like Functionality and Adaptivity. Accounts of Chemical Research (2017). DOI: 10.1021/acs.accounts.6b00512
- ↑ 7.0 7.1 7.2 7.3 7.4 L. Otrin, C. Kleineberg, L. Caire da Silva, K. Landfester, I. Ivanov, M. Wang, C. Bednarz, K. Sundmacher, and T. Vidaković‐Koch, Artificial Organelles for Energy Regeneration. Advanced Biosystems (2019). DOI: 10.1002/adbi.201800323
- ↑ 8.0 8.1 8.2 8.3 8.4 8.5 H. R. Sikkema, B. F. Gaastra, T. Pols, and B. Poolman, Cell Fuelling and Metabolic Energy Conservation in Synthetic Cells. ChemBioChem (2019). DOI: 10.1002/cbic.201900398
- ↑ 9.0 9.1 9.2 9.3 S. Jeong, H. T. Nguyen, C. H. Kim, M. N. Ly, and K. Shin, Toward Artificial Cells: Novel Advances in Energy Conversion and Cellular Motility. Advanced Functional Materials (2020). DOI: 10.1002/adfm.201907182
- ↑ S. Berhanu, T. Ueda, and Y. Kuruma, Artificial photosynthetic cell producing energy for protein synthesis. Nature Communications (2019). DOI: 10.1038/s41467-019-09147-4
- ↑ 11.0 11.1 P. Schwille, J. Spatz, K. Landfester, E. Bodenschatz, S. Herminghaus, V. Sourjik, T. J. Erb, P. Bastiaens, R. Lipowsky, A. Hyman, P. Dabrock, J.-C. Baret, T. Vidakovic‐Koch, P. Bieling, R. Dimova, H. Mutschler, T. Robinson, T.-Y. D. Tang, S. Wegner, and K. Sundmacher, MaxSynBio: Avenues Towards Creating Cells from the Bottom Up. Angewandte Chemie International Edition (2018). DOI: 10.1002/anie.201802288