Peptide‐Metal Cation Coacervate Microdroplets as Membrane‐free Protocells with Enhanced Light‐Induced Catalysis
Source abstract
Abstract
ABSTRACT Membrane‐free coacervates, typically formed through electrostatic interactions between oppositely charged polyelectrolytes, have been extensively utilized as artificial life‐like systems in protocell research, providing valuable insights into the origin of life. However, considering that inorganic metal ions may have been more abundant under early Earth conditions, it is plausible that these metal ions played a significant role in prebiotic compartmentalization. In this study, we present a novel coacervate protocell formed via liquid‐liquid phase separation (LLPS) of simple anionic polypeptides, induced by electrostatic and coordination interactions with inorganic metal cations, using divalent zinc ions as a specific example due to their prebiotic availability and biological relevance. The peptide‐zinc ion coacervate microdroplet exhibits liquid‐like properties, client partitioning, and enhanced catalysis comparable to those of typical polyelectrolyte coacervates. By integrating experimental results and theoretical simulations, we identify two kinetic pathways to phase separation mediated by the coordination mode at varying zinc ion concentrations, resulting in the formation of nonequilibrium gel‐like condensates or droplets that further contribute to distinct light‐induced catalytic efficiency. Overall, our work highlights that peptide‐metal ion interaction‐driven compartmentalization, as prebiotic microreactors, could have facilitated primitive biochemical reactions on early Earth, thus offering a plausible and diverse pathway for the emergence of protocells.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Origins and Evolution of Life · Supramolecular Self-Assembly in Materials · Paleontology and Stratigraphy of Fossils
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry Chemical Engineering and Resource Utilization Northeast Forestry University Harbin Heilongjiang China
State Key Laboratory of Advanced Inorganic Fibers and Composites School of Chemistry and Chemical Engineering Harbin Institute of Technology Harbin Heilongjiang China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Heilongjiang Province
References (55)
Show source-provided references
1. 10.1126/science.106848910.1126/science.1068489 ↗
2. 10.1021/ar200281t10.1021/ar200281t ↗
3. 10.1021/jacs.5c0995010.1021/jacs.5c09950 ↗
4. 10.1002/advs.20230583710.1002/advs.202305837 ↗
5. 10.1021/acs.biomac.4c0014310.1021/acs.biomac.4c00143 ↗
6. 10.1002/cbic.20250044810.1002/cbic.202500448 ↗
7. 10.1021/acs.biomac.3c0071110.1021/acs.biomac.3c00711 ↗
8. 10.1073/pnas.241950712210.1073/pnas.2419507122 ↗
9. 10.1038/s41557‐025‐01827‐710.1038/s41557‐025‐01827‐7 ↗
10. 10.1038/s41467‐025‐60541‐710.1038/s41467‐025‐60541‐7 ↗
11. 10.1021/jacs.5c0158110.1021/jacs.5c01581 ↗
12. 10.1038/s41467‐025‐57069‐110.1038/s41467‐025‐57069‐1 ↗
13. 10.1002/anie.20250531610.1002/anie.202505316 ↗
14. 10.1038/s41557‐025‐01800‐410.1038/s41557‐025‐01800‐4 ↗
15. 10.1038/s44160‐025‐00844‐110.1038/s44160‐025‐00844‐1 ↗
16. 10.1021/jacs.4c1705410.1021/jacs.4c17054 ↗
17. 10.1002/anie.20251226610.1002/anie.202512266 ↗
18. Oparin A. I. · 1938
19. 10.1002/smtd.20230049610.1002/smtd.202300496 ↗
20. 10.1002/smtd.20230004210.1002/smtd.202300042 ↗
21. 10.1016/j.jcis.2025.13748610.1016/j.jcis.2025.137486 ↗
22. 10.1021/accountsmr.2c0023910.1021/accountsmr.2c00239 ↗
23. 10.1002/anie.20242260110.1002/anie.202422601 ↗
24. 10.1039/d0cs00307g10.1039/d0cs00307g ↗
25. 10.1038/s41557‐021‐00788‐x10.1038/s41557‐021‐00788‐x ↗
26. 10.1038/s41578‐022‐00528‐810.1038/s41578‐022‐00528‐8 ↗
27. 10.1038/s41467‐023‐44278‐910.1038/s41467‐023‐44278‐9 ↗
28. 10.1038/s41467‐025‐57772‐z10.1038/s41467‐025‐57772‐z ↗
29. 10.1039/D5SC02170G10.1039/D5SC02170G ↗
30. 10.1038/s41929‐018‐0116‐310.1038/s41929‐018‐0116‐3 ↗
31. 10.1126/sciadv.adi734710.1126/sciadv.adi7347 ↗
32. 10.1038/s41467‐020‐19391‐810.1038/s41467‐020‐19391‐8 ↗
33. 10.1007/s10118‐022‐2763‐810.1007/s10118‐022‐2763‐8 ↗
34. 10.1016/j.cbpa.2023.10230810.1016/j.cbpa.2023.102308 ↗
35. 10.1038/s41467‐024‐54588‐110.1038/s41467‐024‐54588‐1 ↗
36. 10.1111/jnc.1575610.1111/jnc.15756 ↗
37. 10.1074/jbc.AC120.01316610.1074/jbc.AC120.013166 ↗
38. 10.1002/chem.20220141910.1002/chem.202201419 ↗
39. 10.1186/1759‐2208‐3‐210.1186/1759‐2208‐3‐2 ↗
40. 10.1073/pnas.96.16.883510.1073/pnas.96.16.8835 ↗
41. 10.1021/acs.chemrev.9b0066410.1021/acs.chemrev.9b00664 ↗
42. 10.1126/science.117.3046.510.1126/science.117.3046.5 ↗
43. 10.1016/j.cbpc.2006.12.01810.1016/j.cbpc.2006.12.018 ↗
44. 10.1021/acsomega.2c0763510.1021/acsomega.2c07635 ↗
45. 10.1039/C5RA11915D10.1039/C5RA11915D ↗
46. 10.1002/app.4712610.1002/app.47126 ↗
47. 10.1002/mabi.20210046210.1002/mabi.202100462 ↗
48. 10.1021/bi602596210.1021/bi6025962 ↗
49. 10.1021/acsnano.9b0344410.1021/acsnano.9b03444 ↗
50. 10.1186/1745‐6150‐4‐2710.1186/1745‐6150‐4‐27 ↗
51. 10.1002/cbdv.20079005710.1002/cbdv.200790057 ↗
52. 10.1073/pnas.69.3.76510.1073/pnas.69.3.765 ↗
53. 10.1038/s41467‐023‐43272‐510.1038/s41467‐023‐43272‐5 ↗
54. 10.1038/ngeo167910.1038/ngeo1679 ↗
55. 10.1073/pnas.11177741010.1073/pnas.111777410 ↗