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Maleimide-mediated methodologies are among the most used in bioconjugation. [5] [6] Due to fast reactions and high selectivity towards cysteine residues in proteins, a large variety of maleimide heterobifunctional reagents are used for the preparation of targeted therapeutics, assemblies for studying proteins in their biological context, protein-based microarrays, or proteins immobilisation. [7]
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This core structure includes a central maleimide group with two indole groups attached. Examples of bisindolylmaleimide derivatives include: Bisindolylmaleimide I
Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC) is a heterobifunctional amine-to-sulfhydryl crosslinker, which contains two reactive groups at opposite ends: N-hydroxysuccinimide-ester and maleimide, reactive with amines and thiols respectively.
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The MEROPS online database for peptidases and their inhibitors: NEM [permanent dead link ]; The bifunctional analogues such as p-NN′-phenylenebismaleimide can be used as cross-linking reagent for cystine residues.
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At neutral pH, protein thiol groups specifically react with the functional groups methanethiosulfonate, maleimide, and iodoacetamide, creating a covalent bond with the amino acid Cys. [4] Spin labels are a unique molecular reporter, in that they are paramagnetic (contain an unpaired electron).