Issue 82, 2016

Chloromethyl-triazole: a new motif for site-selective pseudo-acylation of proteins

Abstract

Rapid, site-selective modification of cysteine residues with chloromethyl-triazole derivatives generates pseudo-acyl sLys motifs, mimicking important post-translational modifications. Near-native biotinylation of peptide and protein substrates is shown to be site-selective and modified histone H4 retains functional activity.

Graphical abstract: Chloromethyl-triazole: a new motif for site-selective pseudo-acylation of proteins

Supplementary files

Article information

Article type
Communication
Submitted
18 Aug 2016
Accepted
13 Sep 2016
First published
13 Sep 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 12230-12232

Chloromethyl-triazole: a new motif for site-selective pseudo-acylation of proteins

R. C. Brewster, G. C. Gavins, B. Günthardt, S. Farr, K. M. Webb, P. Voigt and A. N. Hulme, Chem. Commun., 2016, 52, 12230 DOI: 10.1039/C6CC06801D

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