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Published September 16, 2011 | Published
Journal Article Open

Site-Specific Protein Modification with a Dirhodium Metallopeptide Catalyst

Abstract

A new method for chemical protein modification is presented utilizing a dirhodium metallopeptide catalyst. The combination of peptide-based molecular recognition and a dirhodium catalyst with broad side-chain scope enables site-specific protein functionalization. The scope and utility of dirhodium-catalyzed biomolecule modification is expanded to allow reaction at physiological pH and in biologically relevant buffer solutions. Specific protein modification is possible directly in E. coli lysate, demonstrating the remarkable activity and specificity of the designed metallopeptide catalyst. Furthermore, a new biotin-diazo conjugate 1b is presented that allows affinity tagging of target proteins.

Copyright and License

© 2011 American Chemical Society.

Acknowledgement

We thank J. Hartgerink and E. Bakota for assistance with peptide synthesis and J. Silberg, K. Matthews, and S. Liu for sharing expertise in recombinant expression. We thank S. Matsuda for helpful discussions, B. Bartel and S. Ratzel for assistance with Western blot techniques, and J. McNew for access to gel imaging instrumentation. B.V.P. acknowledges support from a J. Evans Attwell-Welch Post-doctoral Fellowship. This research is supported by a research grant from the John S. Dunn Gulf Coast Consortium for Chemical Genomics Robert A. Welch Collaborative Grant Program, the Robert A. Welch Foundation research grants C-1680 and L-C-0003, and an NSF CAREER award (CHE-1055569).

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January 29, 2024
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