Designing Selectivity in Dirhodium Metallopeptide Catalysts for Protein Modification

Bioconjug Chem. 2017 Feb 15;28(2):659-665. doi: 10.1021/acs.bioconjchem.6b00716. Epub 2017 Jan 17.

Abstract

The ability to chemically alter proteins is important for broad areas of chemical biology, biophysics, and medicine. Chemical catalysts for protein modification, and particularly rhodium(II) conjugates, represent an important new approach to protein modification that develops novel functionalization approaches while shedding light on the development of selective chemistries in complex environments. Here, we elucidate the reaction parameters that allow selective catalysis and even discrimination among highly similar proteins. Furthermore, we show that quantifying modification allows the measurement of competitive ligand affinity, permitting straightforward measurement of protein-peptide interactions and inhibitors thereof. Taken as a whole, rhodium(II) conjugates replicate many features of enzymes in an entirely chemical construct.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry
  • Amino Acid Sequence
  • Azo Compounds / chemistry
  • Biotin / chemistry
  • Catalysis
  • Humans
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck) / chemistry
  • Models, Molecular
  • Peptides / chemistry*
  • Proteins / chemistry*
  • Rhodium / chemistry*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • src Homology Domains

Substances

  • Alkynes
  • Azo Compounds
  • Peptides
  • Proteins
  • Biotin
  • Rhodium
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck)