Two-component covalent inhibitor

Bioorg Med Chem. 2013 Apr 1;21(7):1988-91. doi: 10.1016/j.bmc.2013.01.021. Epub 2013 Jan 22.

Abstract

Inhibitors that covalently damage proteins or nucleic acids offer great potency, but are difficult to rationally design and suffer from poor specificity. Here we outline a general concept for constructing covalent inhibitors, called the two-component covalent inhibitor (TCCI). The approach takes advantage of two ligand analogs equipped with pre-reactive groups. Binding of the analogs to the adjacent sites of a target biopolymer brings the pre-reactive groups in close proximity and causes their interaction followed by covalent damage of the target. In the present study we used light-activated pre-reactive groups to inactivate a DNA polymerase. It was found that the efficiency of a traditional single-component inhibitor was greatly reduced in the presence of a non-target protein, while the TCCI was not significantly affected. Our findings suggest that TCCI approach has advantages in inactivation of biopolymers in complex multi-component systems.

Publication types

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

MeSH terms

  • Bacteriophage T4 / chemistry
  • Bacteriophage T4 / enzymology*
  • Binding Sites
  • DNA-Directed DNA Polymerase / chemistry
  • DNA-Directed DNA Polymerase / metabolism
  • Drug Design*
  • Light
  • Nucleic Acid Synthesis Inhibitors*
  • Protein Binding
  • Thymine Nucleotides / chemistry*
  • Thymine Nucleotides / pharmacology*

Substances

  • Nucleic Acid Synthesis Inhibitors
  • Thymine Nucleotides
  • DNA-Directed DNA Polymerase
  • thymidine 5'-triphosphate