journal article·2026-04

Electrogenic protein condensates as intracellular electrochemical reactors

Wen Yu, Yuefeng Ma, Leshan Yang, Yanrun Zhou, Xinrui Liu, Yifan Dai

Nature Materials· Volume 25· Issue 4
Publisher page

Abstract

Charged surfaces in aqueous solution establish electric double layers that modulate interfacial electron transfer and drive redox chemistry. However, the capability to engineer the interfacial electrochemical environments of soft biomaterials to enable electron generation for chemical reactions has not been realized. Here we show that genetically encoded biomaterials that can undergo self-assembly into protein condensates can be engineered to function as electrochemical reactors. We establish the fundamental principles that govern the sequence-electrochemical property relationship of protein condensates, thereby programming their electrogenic behaviours. We demonstrate the applications of protein condensates in various electrochemical reactions in vitro. We also deploy these condensates in biological cells as living materials for intracellular nanoparticle synthesis, pollutant degradation and antibiotic-free inhibition of bacteria through artificial ferroptosis. These intrinsic electrogenic materials offer a biomaterial platform that could be used as a clean and sustainable energy source for the development of next-generation bioelectrochemical devices.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Microbial Fuel Cells and Bioremediation · Molecular Junctions and Nanostructures · Metalloenzymes and iron-sulfur proteins

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (49)

Show source-provided references
1. McCarty, L. S. & Whitesides, G. M. Electrostatic charging due to separation of ions at interfaces: contact electrification of ionic electrets. Angew. Chem. Int. Ed. 47, 2188–2207 (2008).10.1002/anie.200701812 ↗
2. Lin, S., Chen, X. & Wang, Z. L. Contact electrification at the liquid–solid interface. Chem. Rev. 122, 5209–5232 (2022).10.1021/acs.chemrev.1c00176 ↗
3. Lacks, D. J. & Shinbrot, T. Long-standing and unresolved issues in triboelectric charging. Nat. Rev. Chem. 3, 465–476 (2019).10.1038/s41570-019-0115-1 ↗
4. Shi, L. et al. Water structure and electric fields at the interface of oil droplets. Nature 640, 87–93 (2025).10.1038/s41586-025-08702-y ↗
5. Lee, J. K. et al. Spontaneous generation of hydrogen peroxide from aqueous microdroplets. Proc. Natl Acad. Sci. USA 116, 19294–19298 (2019).10.1073/pnas.1911883116 ↗
6. Bredenbeck, J., Ghosh, A., Nienhuys, H.-K. & Bonn, M. Interface-specific ultrafast two-dimensional vibrational spectroscopy. Acc. Chem. Res. 42, 1332–1342 (2009).10.1021/ar900016c ↗
7. Galembeck, F., Santos, L. P., Burgo, T. A. L. & Galembeck, A. The emerging chemistry of self-electrified water interfaces. Chem. Soc. Rev. 53, 2578–2602 (2024).10.1039/D3CS00763D ↗
8. Liu, C. & Bard, A. J. Electrostatic electrochemistry at insulators. Nat. Mater. 7, 505–509 (2008).10.1038/nmat2160 ↗
9. Gonella, G. et al. Water at charged interfaces. Nat. Rev. Chem. 5, 466–485 (2021).10.1038/s41570-021-00293-2 ↗
10. Chen, B. et al. Water–solid contact electrification causes hydrogen peroxide production from hydroxyl radical recombination in sprayed microdroplets. Proc. Natl Acad. Sci. USA 119, e2209056119 (2022).10.1073/pnas.2209056119 ↗
11. Chen, H. et al. Microdroplet chemistry with unactivated droplets. J. Am. Chem. Soc. 147, 11399–11406 (2025).10.1021/jacs.5c01072 ↗
12. Colussi, A. J. Mechanism of hydrogen peroxide formation on sprayed water microdroplets. J. Am. Chem. Soc. 145, 16315–16317 (2023).10.1021/jacs.3c04643 ↗
13. Gan, T. et al. Unveiling Janus chemical processes in contact-electro-chemistry through oxygen reduction reactions. J. Am. Chem. Soc. 147, 25407–25416 (2025).10.1021/jacs.5c05124 ↗
14. Wang, Z. et al. Contact-electro-catalysis for the degradation of organic pollutants using pristine dielectric powders. Nat. Commun. 13, 130 (2022).10.1038/s41467-021-27789-1 ↗
15. Dai, Y., Wang, Z.-G. & Zare, R. N. Unlocking the electrochemical functions of biomolecular condensates. Nat. Chem. Biol. 20, 1420–1433 (2024).10.1038/s41589-024-01717-y ↗
16. Dai, Y. et al. Biomolecular condensates regulate cellular electrochemical equilibria. Cell 187, 5951–5966.e18 (2024).10.1016/j.cell.2024.08.018 ↗
17. Watson, J. L. et al. Macromolecular condensation buffers intracellular water potential. Nature 623, 842–852 (2023).10.1038/s41586-023-06626-z ↗
18. Dai, Y. et al. Interface of biomolecular condensates modulates redox reactions. Chem 9, 1594–1609 (2023).10.1016/j.chempr.2023.04.001 ↗
19. Zhang, P., Alsaifi, N. M., Wu, J. & Wang, Z.-G. Polyelectrolyte complex coacervation: effects of concentration asymmetry. J. Chem. Phys. https://doi.org/10.1063/1.5028524 (2018).10.1063/1.5028524 ↗
20. Yu, W. et al. Aging-dependent evolving electrochemical potentials of biomolecular condensates regulate their physicochemical activities. Nat. Chem. 17, 756–766 (2025).10.1038/s41557-025-01762-7 ↗
21. Faraday, M. Experimental researches in electricity: eighteenth series. Proc. R. Soc. Lond. https://doi.org/10.1098/rspl.1837.0215 (1843).10.1098/rspl.1837.0215 ↗
22. Welsh, T. J. et al. Surface electrostatics govern the emulsion stability of biomolecular condensates. Nano Lett. 22, 612–621 (2022).10.1021/acs.nanolett.1c03138 ↗
23. Chen, M. W. et al. Transition-state-dependent spontaneous generation of reactive oxygen species by Aβ assemblies encodes a self-regulated positive feedback loop for aggregate formation. J. Am. Chem. Soc. 147, 8267–8279 (2025).10.1021/jacs.4c15532 ↗
24. Chen, M. W. et al. Condenzymes: biomolecular condensates with inherent catalytic activities. Preprint at bioRxiv https://doi.org/10.1101/2024.07.06.602359 (2025).10.1101/2024.07.06.602359 ↗
25. Rowe, G. K. & Creager, S. E. Interfacial solvation and double-layer effects on redox reactions in organized assemblies. J. Phys. Chem. 98, 5500–5507 (1994).10.1021/j100072a017 ↗
26. Dai, Y. et al. Programmable synthetic biomolecular condensates for cellular control. Nat. Chem. Biol. 19, 518–528 (2023).10.1038/s41589-022-01252-8 ↗
27. Bard, A. J., Faulkner, L. R. & White, H. S. Electrochemical Methods: Fundamentals and Applications (Wiley, 2022).
28. Wang, Z. et al. A contact-electro-catalysis process for producing reactive oxygen species by ball milling of triboelectric materials. Nat. Commun. 15, 757 (2024).10.1038/s41467-024-45041-4 ↗
29. Liu, J. et al. Nonaqueous contact-electro-chemistry via triboelectric charge. J. Am. Chem. Soc. 146, 31574–31584 (2024).10.1021/jacs.4c09318 ↗
30. Li, L. & Cui, C. Bulk water redox chemistry enables radical-mediated C–C coupling in CO2 electroreduction. Nat. Chem. https://doi.org/10.1038/s41557-025-01948-z (2025).10.1038/s41557-025-01948-z ↗
31. Wang, L., Fu, Y., Li, Q. & Wang, Z. EPR evidence for mechanistic diversity of Cu(II)/peroxygen oxidation systems by tracing the origin of DMPO spin adducts. Environ. Sci. Technol. 56, 8796–8806 (2022).10.1021/acs.est.2c00459 ↗
32. Li, L., Abe, Y., Mashino, T., Mochizuki, M. & Miyata, N. Signal enhancement in ESR spin-trapping for hydroxyl radicals. Anal. Sci. 19, 1083–1084 (2003).10.2116/analsci.19.1083 ↗
33. Farag, M., Borcherds, W. M., Bremer, A., Mittag, T. & Pappu, R. V. Phase separation of protein mixtures is driven by the interplay of homotypic and heterotypic interactions. Nat. Commun. 14, 5527 (2023).10.1038/s41467-023-41274-x ↗
34. Berg, J. C. An Introduction to Interfaces & Colloids: The Bridge to Nanoscience (World Scientific, 2010).10.1142/7579 ↗
35. Lyklema, J. (ed) Fundamentals of Interface and Colloid Science: Soft Colloids Vol. 5 (Elsevier, 2005).
36. Gawande, M. B. et al. Cu and Cu-based nanoparticles: synthesis and applications in catalysis. Chem. Rev. 116, 3722–3811 (2016).10.1021/acs.chemrev.5b00482 ↗
37. Yang, X., Yang, M., Pang, B., Vara, M. & Xia, Y. Gold nanomaterials at work in biomedicine. Chem. Rev. 115, 10410–10488 (2015).10.1021/acs.chemrev.5b00193 ↗
38. Luty-Błocho, M., Wojnicki, M., Grzonka, J., Kurzydłowski, K. J. & Fitzner, K. Linking the gold nanoparticles formation kinetics with their morphology. Int. J. Chem. Kinet. 50, 204–214 (2018).10.1002/kin.21152 ↗
39. Zhang, H. et al. Bacteria photosensitized by intracellular gold nanoclusters for solar fuel production. Nat. Nanotechnol. 13, 900–905 (2018).10.1038/s41565-018-0267-z ↗
40. Lin, L. et al. Catalytic gold nanoparticles immobilized on yeast: from biosorption to bioreduction. Chem. Eng. J. 225, 857–864 (2013).10.1016/j.cej.2013.04.003 ↗
41. Chung, K.-T. & Stevens, S. E. Jr Degradation azo dyes by environmental microorganisms and helminths. Environ. Toxicol. Chem. 12, 2121–2132 (1993).
42. Jing, W. et al. Ferrous gluconate triggers ferroptosis in Escherichia coli: implications of lipid peroxidation and DNA damage. Microbiol. Res. 284, 127711 (2024).10.1016/j.micres.2024.127711 ↗
43. Kritsiligkou, P. et al. Proteome-wide tagging with an H2O2 biosensor reveals highly localized and dynamic redox microenvironments. Proc. Natl Acad. Sci. USA 120, e2314043120 (2023).10.1073/pnas.2314043120 ↗
44. Chao, Y. & Shum, H. C. Emerging aqueous two-phase systems: from fundamentals of interfaces to biomedical applications. Chem. Soc. Rev. 49, 114–142 (2020).10.1039/C9CS00466A ↗
45. Yang, L., Yu, W., Zeng, X. & Dai, Y. Asymmetry in hydrophobicity induces electric potential in non-charged protein condensates. Preprint at bioRxiv https://doi.org/10.1101/2025.10.15.682625 (2025).10.1101/2025.10.15.682625 ↗
46. Petek, H. & Zhao, J. Ultrafast interfacial proton-coupled electron transfer. Chem. Rev. 110, 7082–7099 (2010).10.1021/cr1001595 ↗
47. LaCour, R. A., Heindel, J. P., Zhao, R. & Head-Gordon, T. The role of interfaces and charge for chemical reactivity in microdroplets. J. Am. Chem. Soc. 147, 6299–6317 (2025).10.1021/jacs.4c15493 ↗
48. Quiroz, F. G. & Chilkoti, A. Sequence heuristics to encode phase behaviour in intrinsically disordered protein polymers. Nat. Mater. 14, 1164–1171 (2015).10.1038/nmat4418 ↗
49. Hassouneh, W., Christensen, T. & Chilkoti, A. Elastin-like polypeptides as a purification tag for recombinant proteins. Curr. Protoc. Protein Sci. 61, 6.11. 1–16.11.16 (2010).10.1002/0471140864.ps0611s61 ↗