4.6 Article

Site-Specific Protein Modification with a Dirhodium Metallopeptide Catalyst

Journal

ACS CHEMICAL BIOLOGY
Volume 6, Issue 9, Pages 920-925

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cb2001523

Keywords

-

Funding

  1. John S. Dunn Gulf Coast Consortium for Chemical Genomics
  2. Robert A. Welch Foundation [C-1680, L-C-0003]
  3. NSF [CHE-1055569]
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [0947054, 1055569] Funding Source: National Science Foundation

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available