Abstract
Bromo- and thiomaleimides are shown to serve as highly effective quenchers of a covalently attached fluorophore. Reactions with thiols that lead to removal of the maleimide conjugation, or detachment of the fluorophore from the maleimide, result in 'turn-on' of the fluorescence. These reagents thus offer opportunities in thiol sensing and intracellular reporting. © The Royal Society of Chemistry.
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CITATION STYLE
Youziel, J., Akhbar, A. R., Aziz, Q., Smith, M. E. B., Caddick, S., Tinker, A., & Baker, J. R. (2014). Bromo- and thiomaleimides as a new class of thiol-mediated fluorescence “turn-on” reagents. Organic and Biomolecular Chemistry, 12(4), 557–560. https://doi.org/10.1039/c3ob42141d
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