The Rhomboid Superfamily: Structural Mechanisms and Chemical Biology Opportunities

Trends Biochem Sci. 2018 Sep;43(9):726-739. doi: 10.1016/j.tibs.2018.06.009. Epub 2018 Jul 25.

Abstract

The rhomboid superfamily of transmembrane (TM) proteins includes intramembrane serine proteases and several classes of pseudoprotease. Rhomboid-like proteins occur widely across evolution and comprise biologically important regulators of fate of membrane proteins, influencing their proteolysis, trafficking, or degradation. In this review, we discuss how structural and mechanistic insights into the action of rhomboid proteases can inform on the mechanism of the pseudoproteases, and discuss the impact of structural understanding on the development of inhibitors and other chemical biology tools for these proteins. Development of modulators would be particularly relevant for the iRhoms, which are key regulators of ADAM17 and, hence, tumor necrosis factor (TNF) and epidermal growth factor receptor (EGFR) signaling, two medically important pathways.

Keywords: inhibitor; intramembrane protease; mechanism; pseudoenzyme; signaling; structure.

Publication types

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

MeSH terms

  • ADAM17 Protein / genetics
  • ADAM17 Protein / metabolism*
  • Animals
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Protein Transport / physiology
  • Proteolysis*
  • Signal Transduction / physiology*
  • Structure-Activity Relationship
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Membrane Proteins
  • Tumor Necrosis Factor-alpha
  • ADAM17 Protein
  • ADAM17 protein, human