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Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation

[Image: see text] Models of chemical evolution are central to advancing origins of life research. To design more lifelike systems, we must expand our understanding of molecular selection mechanisms. Here, we show two selection modes that produce evolving populations of self-reproducing species, form...

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Autores principales: Howlett, Michael G., Scanes, Robert J. H., Fletcher, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479773/
https://www.ncbi.nlm.nih.gov/pubmed/34604845
http://dx.doi.org/10.1021/jacsau.1c00138
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author Howlett, Michael G.
Scanes, Robert J. H.
Fletcher, Stephen P.
author_facet Howlett, Michael G.
Scanes, Robert J. H.
Fletcher, Stephen P.
author_sort Howlett, Michael G.
collection PubMed
description [Image: see text] Models of chemical evolution are central to advancing origins of life research. To design more lifelike systems, we must expand our understanding of molecular selection mechanisms. Here, we show two selection modes that produce evolving populations of self-reproducing species, formed through thiol–disulfide exchange. Competition between thiol precursors can give clear succession patterns based on steric factors, an intrinsic property. A separate, emergent selection mechanism—dynamic activating metathesis—was found when exploring competing disulfide precursors. These experiments reveal that additional species generated in the mixture open up alternative reaction pathways to form self-reproducing products. Thus, increased compositional complexity provides certain species with a unique competitive advantage at the expense of others.
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spelling pubmed-84797732021-09-30 Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation Howlett, Michael G. Scanes, Robert J. H. Fletcher, Stephen P. JACS Au [Image: see text] Models of chemical evolution are central to advancing origins of life research. To design more lifelike systems, we must expand our understanding of molecular selection mechanisms. Here, we show two selection modes that produce evolving populations of self-reproducing species, formed through thiol–disulfide exchange. Competition between thiol precursors can give clear succession patterns based on steric factors, an intrinsic property. A separate, emergent selection mechanism—dynamic activating metathesis—was found when exploring competing disulfide precursors. These experiments reveal that additional species generated in the mixture open up alternative reaction pathways to form self-reproducing products. Thus, increased compositional complexity provides certain species with a unique competitive advantage at the expense of others. American Chemical Society 2021-08-16 /pmc/articles/PMC8479773/ /pubmed/34604845 http://dx.doi.org/10.1021/jacsau.1c00138 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Howlett, Michael G.
Scanes, Robert J. H.
Fletcher, Stephen P.
Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation
title Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation
title_full Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation
title_fullStr Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation
title_full_unstemmed Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation
title_short Selection between Competing Self-Reproducing Lipids: Succession and Dynamic Activation
title_sort selection between competing self-reproducing lipids: succession and dynamic activation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479773/
https://www.ncbi.nlm.nih.gov/pubmed/34604845
http://dx.doi.org/10.1021/jacsau.1c00138
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