Diverse functions of the prion protein - Does proteolytic processing hold the key?

Biochim Biophys Acta Mol Cell Res. 2017 Nov;1864(11 Pt B):2128-2137. doi: 10.1016/j.bbamcr.2017.06.022. Epub 2017 Jul 8.

Abstract

Proteolytic processing of the cellular and disease-associated form of the prion protein leads to generation of bioactive soluble prion protein fragments and modifies the structure and function of its cell-bound form. The nature of proteases responsible for shedding, α-, β-, and γ-cleavage of the prion protein are only partially identified and their regulation is largely unknown. Here, we provide an overview of the increasingly multifaceted picture of prion protein proteolysis and shed light on physiological and pathological roles associated with these cleavages. This article is part of a Special Issue entitled: Proteolysis as a Regulatory Event in Pathophysiology edited by Stefan Rose-John.

Keywords: ADAM10; Neurodegeneration; Neuropathology; Prion; Proteolysis; Shedding.

Publication types

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

MeSH terms

  • Animals
  • Humans
  • Prion Diseases / genetics*
  • Prion Diseases / pathology
  • Prion Proteins / genetics*
  • Prion Proteins / metabolism
  • Protein Aggregation, Pathological / genetics
  • Proteolysis*

Substances

  • Prion Proteins