Literature DB >> 23831604

Mechanisms and cellular functions of intramembrane proteases.

Siniša Urban1.   

Abstract

The turn of the millennium coincided with the branding of a fundamentally different class of enzyme - proteases that reside immersed inside the membrane. This new field was the convergence of completely separate lines of research focused on cholesterol homeostasis, Alzheimer's disease, and developmental genetics. None intended their ultimate path, but soon became a richly-integrated fabric for an entirely new field: regulated intramembrane proteolysis. Our aim in this Special Issue is to focus on the ancient and nearly ubiquitous enzymes that catalyze this unexpected yet important reaction. The pace of progress has been dramatic, resulting in a rapidly-expanding universe of known cellular functions, and a paradigm shift in the biochemical understanding of these once heretical enzymes. More recently, the first therapeutic successes have been attained by targeting an intramembrane protease. We consider these advances and identify oncoming opportunities in four parts: growing spectra of cellular roles, insights into biochemical mechanisms, therapeutic strategies, and newly-emerging topics. Recent studies also expose challenges for the future, including non-linear relationships between substrate identification and physiological functions, and the need for potent and specific, not broad-class, inhibitors.
© 2013.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23831604     DOI: 10.1016/j.bbamem.2013.07.001

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  12 in total

1.  Nicastrin functions to sterically hinder γ-secretase-substrate interactions driven by substrate transmembrane domain.

Authors:  David M Bolduc; Daniel R Montagna; Yongli Gu; Dennis J Selkoe; Michael S Wolfe
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-22       Impact factor: 11.205

2.  A subset of membrane-altering agents and γ-secretase modulators provoke nonsubstrate cleavage by rhomboid proteases.

Authors:  Siniša Urban; Syed M Moin
Journal:  Cell Rep       Date:  2014-08-21       Impact factor: 9.423

3.  Orphan enzyme cuts down on sugar.

Authors:  Siniša Urban
Journal:  EMBO J       Date:  2014-11-20       Impact factor: 11.598

Review 4.  A century of cholesterol and coronaries: from plaques to genes to statins.

Authors:  Joseph L Goldstein; Michael S Brown
Journal:  Cell       Date:  2015-03-26       Impact factor: 41.582

5.  Enzymatic Assays for Studying Intramembrane Proteolysis.

Authors:  D M Bolduc; D J Selkoe; M S Wolfe
Journal:  Methods Enzymol       Date:  2016-12-24       Impact factor: 1.600

6.  Interaction of intramembrane metalloprotease SpoIVFB with substrate Pro-σK.

Authors:  Sabyasachi Halder; Daniel Parrell; Douglas Whitten; Michael Feig; Lee Kroos
Journal:  Proc Natl Acad Sci U S A       Date:  2017-11-27       Impact factor: 11.205

7.  Conserved Proline Residues of Bacillus subtilis Intramembrane Metalloprotease SpoIVFB Are Important for Substrate Interaction and Cleavage.

Authors:  Fiona Buchanan; Jordyn VanPortfliet; Sandra Olenic; Daniel Parrell; Lee Kroos
Journal:  J Bacteriol       Date:  2022-01-10       Impact factor: 3.476

8.  Inhibitory proteins block substrate access by occupying the active site cleft of Bacillus subtilis intramembrane protease SpoIVFB.

Authors:  Sandra Olenic; Lim Heo; Michael Feig; Lee Kroos
Journal:  Elife       Date:  2022-04-26       Impact factor: 8.713

9.  Bacillus subtilis Intramembrane Protease RasP Activity in Escherichia coli and In Vitro.

Authors:  Daniel Parrell; Yang Zhang; Sandra Olenic; Lee Kroos
Journal:  J Bacteriol       Date:  2017-09-05       Impact factor: 3.490

10.  Roles of the membrane-reentrant β-hairpin-like loop of RseP protease in selective substrate cleavage.

Authors:  Koichiro Akiyama; Shinya Mizuno; Yohei Hizukuri; Hiroyuki Mori; Terukazu Nogi; Yoshinori Akiyama
Journal:  Elife       Date:  2015-10-08       Impact factor: 8.140

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.