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.
CITATION STYLE
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
Mendeley helps you to discover research relevant for your work.