Understanding intramembrane proteolysis: From protein dynamics to reaction kinetics

D. Langosch, C. Scharnagl, H. Steiner, M. K. Lemberg

Research output: Contribution to journalReview articlepeer-review

89 Scopus citations

Abstract

Intramembrane proteolysis - cleavage of proteins within the plane of a membrane - is a widespread phenomenon that can contribute to the functional activation of substrates and is involved in several diseases. Although different families of intramembrane proteases have been discovered and characterized, we currently do not know how these enzymes discriminate between substrates and non-substrates, how site-specific cleavage is achieved, or which factors determine the rate of proteolysis. Focusing on γ-secretase and rhomboid proteases, we argue that answers to these questions may emerge from connecting experimental readouts, such as reaction kinetics and the determination of cleavage sites, to the structures and the conformational dynamics of substrates and enzymes.

Original languageEnglish
Pages (from-to)318-327
Number of pages10
JournalTrends in Biochemical Sciences
Volume40
Issue number6
DOIs
StatePublished - 1 Jun 2015

Keywords

  • Conformational dynamics
  • Intramembrane proteolysis/protease
  • Presenilin
  • Rhomboid
  • Transmembrane helix
  • γ-secretase

Fingerprint

Dive into the research topics of 'Understanding intramembrane proteolysis: From protein dynamics to reaction kinetics'. Together they form a unique fingerprint.

Cite this