Controlling maleimide hydrolysis allows the modular construction of bromomaleimide-mediated bioconjugates which are either stable or cleavable in an aqueous, thiol-mediated reducing environment. The application of this methodology to reversible protein biotinylation, the irreversible labeling of peptide disulfide bonds and the assembly of stable, fluorescein-labelled glycoprotein mimics is described.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3381635PMC
http://dx.doi.org/10.1039/c1cc11114kDOI Listing

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