Issue 36, 2022

Novel electrochemically-mediated peptide dethiylation in processes relevant to native chemical ligation

Abstract

Here we explore electrochemical dethiylation in processes relevant to Native Chemical Ligation (NCL). NCL's reliance on the redox active amino acid cysteine and β-mercaptamine derivatives suggests a potential role for electrochemistry. We show that the application of a 1 V potential to platinum electrodes in 0.15 M TCEP solution is sufficient to convert Cys to Ala in cyclic peptides, and to cleave the 2-mercapto-2-phenethyl class of acyl transfer auxiliary.

Graphical abstract: Novel electrochemically-mediated peptide dethiylation in processes relevant to native chemical ligation

Supplementary files

Article information

Article type
Paper
Submitted
19 Aug 2022
Accepted
30 Aug 2022
First published
30 Aug 2022
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2022,20, 7343-7350

Novel electrochemically-mediated peptide dethiylation in processes relevant to native chemical ligation

C. M. G. Lamb, J. Shi, J. D. Wilden and D. Macmillan, Org. Biomol. Chem., 2022, 20, 7343 DOI: 10.1039/D2OB01499H

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