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

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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.

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Brewster, R. C., Gavins, G. C., Günthardt, B., Farr, S., Webb, K. M., Voigt, P., & Hulme, A. N. (2016). Chloromethyl-triazole: A new motif for site-selective pseudo-acylation of proteins. Chemical Communications, 52(82), 12230–12232. https://doi.org/10.1039/c6cc06801d

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