Functional interrogation and therapeutic targeting of protein tyrosine phosphatases

Biochem Soc Trans. 2021 Aug 27;49(4):1723-1734. doi: 10.1042/BST20201308.

Abstract

Protein tyrosine phosphatases (PTPs) counteract the enzymatic activity of protein tyrosine kinases to modulate levels of both normal and disease-associated protein tyrosine phosphorylation. Aberrant activity of PTPs has been linked to the progression of many disease states, yet no PTP inhibitors are currently clinically available. PTPs are without a doubt a difficult drug target. Despite this, many selective, potent, and bioavailable PTP inhibitors have been described, suggesting PTPs should once again be looked at as viable therapeutic targets. Herein, we summarize recently discovered PTP inhibitors and their use in the functional interrogation of PTPs in disease states. In addition, an overview of the therapeutic targeting of PTPs is described using SHP2 as a representative target.

Keywords: chemical biology; drug discovery; protein tyrosine phosphatase.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Molecular Weight
  • Mycobacterium tuberculosis / enzymology
  • Protein Tyrosine Phosphatases / antagonists & inhibitors
  • Protein Tyrosine Phosphatases / chemistry
  • Protein Tyrosine Phosphatases / metabolism*
  • Small Molecule Libraries / pharmacology

Substances

  • Enzyme Inhibitors
  • Small Molecule Libraries
  • Protein Tyrosine Phosphatases