Exceptionally high-affinity Ras binders that remodel its effector domain

J Biol Chem. 2018 Mar 2;293(9):3265-3280. doi: 10.1074/jbc.M117.816348. Epub 2017 Dec 27.

Abstract

The Ras proteins are aberrantly activated in a wide range of human cancers, often endowing tumors with aggressive properties and resistance to therapy. Decades of effort to develop direct Ras inhibitors for clinical use have thus far failed, largely because of a lack of adequate small-molecule-binding pockets on the Ras surface. Here, we report the discovery of Ras-binding miniproteins from a naïve library and their evolution to afford versions with midpicomolar affinity to Ras. A series of biochemical experiments indicated that these miniproteins bind to the Ras effector domain as dimers, and high-resolution crystal structures revealed that these miniprotein dimers bind Ras in an unprecedented mode in which the Ras effector domain is remodeled to expose an extended pocket that connects two isolated pockets previously found to engage small-molecule ligands. We also report a Ras point mutant that stabilizes the protein in the open conformation trapped by these miniproteins. These findings provide new tools for studying Ras structure and function and present opportunities for the development of both miniprotein and small-molecule inhibitors that directly target the Ras proteins.

Keywords: Ras protein; X-ray crystallography; cancer; directed evolution; peptides.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Databases, Protein
  • Drug Discovery
  • Models, Molecular
  • Mutation
  • Protein Binding
  • Protein Domains / drug effects
  • Protein Multimerization
  • Protein Structure, Quaternary
  • Proteins / chemistry
  • Proteins / genetics
  • Proteins / metabolism*
  • Proteins / pharmacology*
  • ras Proteins / chemistry*
  • ras Proteins / metabolism*

Substances

  • Proteins
  • ras Proteins

Associated data

  • PDB/1PPT
  • PDB/4OBE
  • PDB/3GFT
  • PDB/4TQ9
  • PDB/4M22
  • PDB/4EPY
  • PDB/5WPL
  • PDB/5WPM
  • PDB/5WLB
  • PDB/5WHA
  • PDB/5WHB
  • PDB/5WHE
  • PDB/5WHD