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Reversible protein affinity-labelling using bromomaleimide-based reagents

Nathani, RI; Chudasama, V; Ryan, CP; Moody, PR; Morgan, RE; Fitzmaurice, RJ; Smith, ME; ... Caddick, S; + view all (2013) Reversible protein affinity-labelling using bromomaleimide-based reagents. Organic & Biomolecular Chemistry , 11 (15) 2408 -2411. 10.1039/c3ob40239h. Green open access

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Abstract

Reversible protein biotinylation is readily affected via conjugation with a bromomaleimide-based reagent followed by reductive cleavage. The intermediate biotinylated protein constructs are stable at physiological temperature and pH 8.0. Quantitative reversibility is elegantly delivered under mild conditions of using a stoichiometric amount of a bis-thiol, thus providing an approach that will be of general interest in chemical biology and proteomics.

Type: Article
Title: Reversible protein affinity-labelling using bromomaleimide-based reagents
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1039/c3ob40239h
Publisher version: http://dx.doi.org/10.1039/c3ob40239h
Language: English
Additional information: This work is licensed under the Creative Commons Attribution License, Attribution 3.0 Unported (CC BY 3.0) http://creativecommons.org/licenses/by/3.0/ which permits unrestricted use, distribution, and reproduction in any medium. However, you must attribute the work to the author (but not in any way that suggests that they endorse you or your use of the work).
UCL classification: UCL
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry
URI: https://discovery.ucl.ac.uk/id/eprint/1388302
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