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Thioesters provide a plausible prebiotic path to proto-peptides

Author

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  • Moran Frenkel-Pinter

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    Georgia Institute of Technology
    The Hebrew University of Jerusalem)

  • Marcos Bouza

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    Georgia Institute of Technology)

  • Facundo M. Fernández

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    Georgia Institute of Technology)

  • Luke J. Leman

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    The Scripps Research Institute)

  • Loren Dean Williams

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    Georgia Institute of Technology)

  • Nicholas V. Hud

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    Georgia Institute of Technology)

  • Aikomari Guzman-Martinez

    (NSF-NASA Center for Chemical Evolution, Georgia Institute of Technology
    University of Puerto Rico, Mayagüez)

Abstract

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.

Suggested Citation

  • Moran Frenkel-Pinter & Marcos Bouza & Facundo M. Fernández & Luke J. Leman & Loren Dean Williams & Nicholas V. Hud & Aikomari Guzman-Martinez, 2022. "Thioesters provide a plausible prebiotic path to proto-peptides," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30191-0
    DOI: 10.1038/s41467-022-30191-0
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    References listed on IDEAS

    as
    1. Pierre Canavelli & Saidul Islam & Matthew W. Powner, 2019. "Peptide ligation by chemoselective aminonitrile coupling in water," Nature, Nature, vol. 571(7766), pages 546-549, July.
    2. Jayanta Nanda & Boris Rubinov & Denis Ivnitski & Rakesh Mukherjee & Elina Shtelman & Yair Motro & Yifat Miller & Nathaniel Wagner & Rivka Cohen-Luria & Gonen Ashkenasy, 2017. "Emergence of native peptide sequences in prebiotic replication networks," Nature Communications, Nature, vol. 8(1), pages 1-9, December.
    3. Rihe Liu & Leslie E. Orgel, 1997. "Oxidative acylation using thioacids," Nature, Nature, vol. 389(6646), pages 52-54, September.
    Full references (including those not matched with items on IDEAS)

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