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

9Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

Lamb, C. M. G., Shi, J., Wilden, J. D., & Macmillan, D. (2022). Novel electrochemically-mediated peptide dethiylation in processes relevant to native chemical ligation. Organic and Biomolecular Chemistry, 20(36), 7343–7350. https://doi.org/10.1039/d2ob01499h

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free