Understanding intramembrane proteolysis: from protein dynamics to reaction kinetics. Issue 6 (June 2015)

• Record Type: Journal Article
• Authors: Langosch, D.; Scharnagl, C.; Steiner, H.; Lemberg, M.K.
• Is Part Of: Trends in biochemical sciences. Volume 40:Issue 6(2015)
• Page Start: 318
• Page End: 327
• Publication Date: 2015-06
• Subjects: intramembrane proteolysis/protease -- transmembrane helix -- presenilin -- γ-secretase -- rhomboid -- conformational dynamics; Biochemistry -- Periodicals; 572
• DOI: 10.1016/j.tibs.2015.04.001
• Languages: English
• ISSNs: 0968-0004

Abstract

Highlights: How intramembrane proteases select their substrates is currently unknown. Helix-destabilizing amino acids within transmembrane helices often facilitate cleavage. Transmembrane helix stability does not distinguish substrates from non-substrates. Mutations affecting cleavage influence transmembrane helix bending. 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.