Published August 10, 2023 | v1
Journal Article Open

Hybrid organic–inorganic structures trigger the formation of primitive cell-like compartments

Abstract

Alkaline hydrothermal vents have become a candidate setting for the origins of life on Earth and beyond. This is due to several key features including the presence of gradients of temperature, redox potential, pH, the availability of inorganic minerals, and the existence of a network of inorganic pore spaces that could have served as primitive compartments. Chemical gardens have long been used as experimental proxies for hydrothermal vents. This paper investigates a set of prebiotic interactions between such inorganic structures and fatty alcohols. The integration of a medium-chain fatty alcohol, decanol, within these inorganic minerals, produced a range of emergent 3 dimensions structures at both macroscopic and microscopic scales. Fatty alcohols can be considered plausible prebiotic amphiphiles that might have assisted the formation of protocellular structures such as vesicles. The experiments presented herein show that neither chemical gardens nor decanol alone promote vesicle formation, but chemical gardens grown in the presence of decanol, which is then integrated into inorganic mineral structures, support vesicle formation. These observations suggest that the interaction of fatty alcohols and inorganic mineral structures could have played an important role in the emergence of protocells, yielding support for the evolution of living cells.

Copyright and License

© 2023 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).

Acknowledgement

We would like to thank Michele Orlandi for the help on the analysis of Energy Dispersive X-ray Spectroscopy (EDXS) data, Nicola Bazzanella for the EDXS image acquisition, and Lucrezia Aversa and Roberto Verucchi for the X-ray Photoelectron Spectroscopy acquisition. We would also like to thank Giorgina Scarduelli for the help in imaging the fatty acid vesicles using the Nikon SIM AX, Graziano Guella for the help during revision, and Department of Cellular Computational and Integrative Biology High Throughput Screening facility for allowing us to use their Tecan plate reader. We would like to thank COST action Chemobrionics (CA17120) and DYNALIFE (CA21169) for giving us the opportunity to meet and conceive important ideas crucial for the manuscript preparation. We would also like to thank Department CIBIO Core Facilities which are supported by the European Regional Development Fund 2014 to 2020. This work was funded in part from the European Union's Horizon 2020 research and innovation programme under grant agreement No. 824060 (project ACDC).

Contributions

S.H., C.I.S.D., J.H.E.C., and M.M.H. designed research; S.H. and F.C. performed research; S.H. and R.J.G.L. analyzed data; and S.H. and S.B. wrote the paper.

Data Availability

All study data are included in the article and/or SI Appendix.

Conflict of Interest

The authors declare no competing interest.

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Additional details

Created:
September 11, 2023
Modified:
September 11, 2023