Literature DB >> 28035818

Designing Selectivity in Dirhodium Metallopeptide Catalysts for Protein Modification.

Samuel C Martin1, Farrukh Vohidov1, Haopei Wang1, Sarah E Knudsen1, Alex A Marzec1, Zachary T Ball1.   

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.

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Year:  2017        PMID: 28035818     DOI: 10.1021/acs.bioconjchem.6b00716

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  1 in total

1.  Aminoquinoline-Rhodium(II) Conjugates as Src-Family SH3 Ligands.

Authors:  Samuel C Martin; Zachary T Ball
Journal:  ACS Med Chem Lett       Date:  2019-09-09       Impact factor: 4.345

  1 in total

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