Rhomboid proteases in human disease: Mechanisms and future prospects

Biochim Biophys Acta Mol Cell Res. 2017 Nov;1864(11 Pt B):2200-2209. doi: 10.1016/j.bbamcr.2017.04.016. Epub 2017 Apr 28.

Abstract

Rhomboids are intramembrane serine proteases that cleave the transmembrane helices of substrate proteins, typically releasing luminal/extracellular domains from the membrane. They are conserved in all branches of life and there is a growing recognition of their association with a wide range of human diseases. Human rhomboids, for example, have been implicated in cancer, metabolic disease and neurodegeneration, while rhomboids in apicomplexan parasites appear to contribute to their invasion of host cells. Recent advances in our knowledge of the structure and the enzyme function of rhomboids, and increasing efforts to identify specific inhibitors, are beginning to provide important insight into the prospect of rhomboids becoming future therapeutic targets. This article is part of a Special Issue entitled: Proteolysis as a Regulatory Event in Pathophysiology edited by Stefan Rose-John.

Keywords: Disease; Enzyme; Protease; Rhomboid; Structure.

Publication types

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

MeSH terms

  • Humans
  • Metabolic Diseases / genetics
  • Molecular Targeted Therapy
  • Neoplasms / genetics
  • Nerve Degeneration / genetics
  • Phylogeny*
  • Proteolysis*
  • Serine Proteases / genetics*
  • Serine Proteases / therapeutic use
  • Substrate Specificity

Substances

  • Serine Proteases