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Thioesters provide a plausible prebiotic path to proto-peptides

It is widely assumed that the condensation of building blocks into oligomers and polymers was important in the origins of life. High activation energies, unfavorable thermodynamics and side reactions are bottlenecks for abiotic peptide formation. All abiotic reactions reported thus far for peptide b...

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Autores principales: Frenkel-Pinter, Moran, Bouza, Marcos, Fernández, Facundo M., Leman, Luke J., Williams, Loren Dean, Hud, Nicholas V., Guzman-Martinez, Aikomari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095695/
https://www.ncbi.nlm.nih.gov/pubmed/35562173
http://dx.doi.org/10.1038/s41467-022-30191-0
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author Frenkel-Pinter, Moran
Bouza, Marcos
Fernández, Facundo M.
Leman, Luke J.
Williams, Loren Dean
Hud, Nicholas V.
Guzman-Martinez, Aikomari
author_facet Frenkel-Pinter, Moran
Bouza, Marcos
Fernández, Facundo M.
Leman, Luke J.
Williams, Loren Dean
Hud, Nicholas V.
Guzman-Martinez, Aikomari
author_sort Frenkel-Pinter, Moran
collection PubMed
description It is widely assumed that the condensation of building blocks into oligomers and polymers was important in the origins of life. High activation energies, unfavorable thermodynamics and side reactions are bottlenecks for abiotic peptide formation. All abiotic reactions reported thus far for peptide bond formation via thioester intermediates have relied on high energy molecules, which usually suffer from short half-life in aqueous conditions and therefore require constant replenishment. Here we report plausible prebiotic reactions of mercaptoacids with amino acids that result in the formation of thiodepsipeptides, which contain both peptide and thioester bonds. Thiodepsipeptide formation was achieved under a wide range of pH and temperature by simply drying and heating mercaptoacids with amino acids. Our results offer a robust one-pot prebiotically-plausible pathway for proto-peptide formation. These results support the hypothesis that thiodepsipeptides and thiol-terminated peptides formed readily on prebiotic Earth and were possible contributors to early chemical evolution.
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spelling pubmed-90956952022-05-13 Thioesters provide a plausible prebiotic path to proto-peptides Frenkel-Pinter, Moran Bouza, Marcos Fernández, Facundo M. Leman, Luke J. Williams, Loren Dean Hud, Nicholas V. Guzman-Martinez, Aikomari Nat Commun Article It is widely assumed that the condensation of building blocks into oligomers and polymers was important in the origins of life. High activation energies, unfavorable thermodynamics and side reactions are bottlenecks for abiotic peptide formation. All abiotic reactions reported thus far for peptide bond formation via thioester intermediates have relied on high energy molecules, which usually suffer from short half-life in aqueous conditions and therefore require constant replenishment. Here we report plausible prebiotic reactions of mercaptoacids with amino acids that result in the formation of thiodepsipeptides, which contain both peptide and thioester bonds. Thiodepsipeptide formation was achieved under a wide range of pH and temperature by simply drying and heating mercaptoacids with amino acids. Our results offer a robust one-pot prebiotically-plausible pathway for proto-peptide formation. These results support the hypothesis that thiodepsipeptides and thiol-terminated peptides formed readily on prebiotic Earth and were possible contributors to early chemical evolution. Nature Publishing Group UK 2022-05-11 /pmc/articles/PMC9095695/ /pubmed/35562173 http://dx.doi.org/10.1038/s41467-022-30191-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Frenkel-Pinter, Moran
Bouza, Marcos
Fernández, Facundo M.
Leman, Luke J.
Williams, Loren Dean
Hud, Nicholas V.
Guzman-Martinez, Aikomari
Thioesters provide a plausible prebiotic path to proto-peptides
title Thioesters provide a plausible prebiotic path to proto-peptides
title_full Thioesters provide a plausible prebiotic path to proto-peptides
title_fullStr Thioesters provide a plausible prebiotic path to proto-peptides
title_full_unstemmed Thioesters provide a plausible prebiotic path to proto-peptides
title_short Thioesters provide a plausible prebiotic path to proto-peptides
title_sort thioesters provide a plausible prebiotic path to proto-peptides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095695/
https://www.ncbi.nlm.nih.gov/pubmed/35562173
http://dx.doi.org/10.1038/s41467-022-30191-0
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