display evolution of unnatural peptides spontaneously cyclized intramolecular nucleophilic aromatic substitutions.

Chem Commun (Camb)

Department of Life and Environmental Sciences, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Yamanashi 400-8510, Japan.

Published: April 2022

We report novel, ribosomally incorporatable, and intramolecularly cysteine-reactive fluorobenzoic acid-derived linkers for SELEX of mRNA-displayed unnatural peptides, which spontaneously cyclized intramolecular nucleophilic aromatic substitutions forming thioethers. With this strategy we identified several novel PCSK9-binding peptides.

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http://dx.doi.org/10.1039/d2cc00584kDOI Listing

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