Palladium Oxidative Addition Complexes for Peptide and Protein Cross-linking
journal contributionposted on 06.02.2018, 00:00 by Koji Kubota, Peng Dai, Bradley L. Pentelute, Stephen L. Buchwald
A new method for cysteine–lysine cross-linking in peptides and proteins using palladium oxidative addition complexes is presented. First, a biarylphosphine-supported palladium reagent is used to transfer an aryl group bearing an O-phenyl carbamate substituent to a cysteine residue. Next, this carbamate undergoes chemoselective acyl substitution by a proximal lysine to form a cross-link. The linkage so formed is stable toward acid, base, oxygen, and external thiol nucleophiles. This method was applied to cross-link cysteine with nearby lysines in sortase A*. Furthermore, we used this method for the intermolecular cross-linking between a peptide and a protein based on the p53-MDM2 interaction. These studies demonstrate the potential for palladium-mediated methods to serve as a platform for the development of future cross-linking techniques for peptides and proteins with natural amino acid residues.
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p 53-MDM interactionaryl groupphenyl carbamate substituentacid residuescross-link cysteineproteinbiarylphosphine-supported palladium reagentProtein Cross-linkinglysinepeptidechemoselective acyl substitutionPalladium Oxidative Addition Complexespalladium oxidative addition complexespalladium-mediated methodsthiol nucleophilesfuture cross-linking techniquescysteine residue