Ribonucleotides and RNA Promote Peptide Chain Growth

All known forms of life use RNA‐mediated polypeptide synthesis to produce the proteins encoded in their genes. Because the principal parts of the translational machinery consist of RNA, it is likely that peptide synthesis was achieved early in the prebiotic evolution of an RNA‐dominated molecular wo...

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Published inAngewandte Chemie International Edition Vol. 56; no. 5; pp. 1219 - 1223
Main Authors Griesser, Helmut, Tremmel, Peter, Kervio, Eric, Pfeffer, Camilla, Steiner, Ulrich E., Richert, Clemens
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 24.01.2017
Wiley Subscription Services, Inc
EditionInternational ed. in English
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Summary:All known forms of life use RNA‐mediated polypeptide synthesis to produce the proteins encoded in their genes. Because the principal parts of the translational machinery consist of RNA, it is likely that peptide synthesis was achieved early in the prebiotic evolution of an RNA‐dominated molecular world. How RNA attracted amino acids and then induced peptide formation in the absence of enzymes has been unclear. Herein, we show that covalent capture of an amino acid as a phosphoramidate favors peptide formation. Peptide coupling is a robust process that occurs with different condensation agents. Kinetics show that covalent capture can accelerate chain growth over oligomerization of the free amino acid by at least one order of magnitude, so that there is no need for enzymatic catalysis for peptide synthesis to begin. Peptide chain growth was also observed on phosphate‐terminated RNA strands. Peptide coupling promoted by ribonucleotides or ribonucleotide residues may have been an important transitional form of peptide synthesis that set in when amino acids were first captured by RNA. Capture accelerates coupling: When amino acids condense with ribonucleotides, they form phosphoramidates, which show faster chain growth than free amino acids, facilitating the transition to a “peptide‐RNA world”.
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201610650