How to awaken your nanomachines: Site-specific activation of focal adhesion kinases through ligand interactions

Prog Biophys Mol Biol. 2015 Oct;119(1):60-71. doi: 10.1016/j.pbiomolbio.2015.06.001. Epub 2015 Jun 17.

Abstract

The focal adhesion kinase (FAK) and the related protein-tyrosine kinase 2-beta (Pyk2) are highly versatile multidomain scaffolds central to cell adhesion, migration, and survival. Due to their key role in cancer metastasis, understanding and inhibiting their functions are important for the development of targeted therapy. Because FAK and Pyk2 are involved in many different cellular functions, designing drugs with partial and function-specific inhibitory effects would be desirable. Here, we summarise recent progress in understanding the structural mechanism of how the tug-of-war between intramolecular and intermolecular interactions allows these protein 'nanomachines' to become activated in a site-specific manner.

Keywords: Adhesome; Calcium signalling; Hybrid methods; Molecular dynamics; Multidomain protein; X-ray crystallography.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Drug Discovery
  • Enzyme Activation / drug effects
  • Focal Adhesion Protein-Tyrosine Kinases / antagonists & inhibitors
  • Focal Adhesion Protein-Tyrosine Kinases / chemistry
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism*
  • Humans
  • Ligands
  • Protein Binding
  • Protein Structure, Tertiary

Substances

  • Ligands
  • Focal Adhesion Protein-Tyrosine Kinases