Literature DB >> 28065265

An Inducible Reconstitution System for the Real-Time Kinetic Analysis of Protease Activity and Inhibition Inside the Membrane.

R P Baker1, S Urban2.   

Abstract

Intramembrane proteases are an ancient and diverse group of multispanning membrane proteins that cleave transmembrane substrates inside the membrane to effect a wide range of biological processes. As proteases, a clear understanding of their function requires kinetic dissection of their catalytic mechanism, but this is difficult to achieve for membrane proteins. Kinetic measurements in detergent systems are complicated by micelle fusion/exchange, which introduces an additional kinetic step and imposes system-specific behaviors (e.g., cooperativity). Conversely, kinetic analysis in proteoliposomes is hindered by premature substrate cleavage during coreconstitution, and lack of methods to quantify proteolysis in membranes in real time. In this chapter, we describe a method for the real-time kinetic analysis of intramembrane proteolysis in model liposomes. Our assay is inducible, because the enzyme is held inactive by low pH during reconstitution, and fluorogenic, since fluorescence emission from the substrate is quenched near lipids but restored upon proteolytic release from the membrane. The precise measurement of initial reaction velocities continuously in real time facilitates accurate steady-state kinetic analysis of intramembrane proteolysis and its inhibition inside the membrane environment. Using real data we describe a step-by-step strategy to implement this assay for essentially any intramembrane protease.
© 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alzheimer's disease; Cancer; Cell signaling; ER-associated degradation; Gamma-secretase; Malaria; Membrane protein; Parkinson's disease; Presenilin; Protease; Regulated intramembrane proteolysis; Site-2 protease

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Year:  2016        PMID: 28065265      PMCID: PMC5224909          DOI: 10.1016/bs.mie.2016.10.025

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  38 in total

1.  Structural analysis of a rhomboid family intramembrane protease reveals a gating mechanism for substrate entry.

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Journal:  Nat Struct Mol Biol       Date:  2006-11-10       Impact factor: 15.369

2.  Crystal structure of a rhomboid family intramembrane protease.

Authors:  Yongcheng Wang; Yingjiu Zhang; Ya Ha
Journal:  Nature       Date:  2006-10-11       Impact factor: 49.962

3.  Functional and evolutionary implications of enhanced genomic analysis of rhomboid intramembrane proteases.

Authors:  Marius K Lemberg; Matthew Freeman
Journal:  Genome Res       Date:  2007-10-15       Impact factor: 9.043

4.  Complementation cloning of S2P, a gene encoding a putative metalloprotease required for intramembrane cleavage of SREBPs.

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Journal:  Mol Cell       Date:  1997-12       Impact factor: 17.970

5.  Sterol-regulated release of SREBP-2 from cell membranes requires two sequential cleavages, one within a transmembrane segment.

Authors:  J Sakai; E A Duncan; R B Rawson; X Hua; M S Brown; J L Goldstein
Journal:  Cell       Date:  1996-06-28       Impact factor: 41.582

6.  Cooperative folding of a polytopic α-helical membrane protein involves a compact N-terminal nucleus and nonnative loops.

Authors:  Wojciech Paslawski; Ove K Lillelund; Julie Veje Kristensen; Nicholas P Schafer; Rosanna P Baker; Sinisa Urban; Daniel E Otzen
Journal:  Proc Natl Acad Sci U S A       Date:  2015-06-08       Impact factor: 11.205

7.  Examination of the protein composition of the cell envelope of Escherichia coli by polyacrylamide gel electrophoresis.

Authors:  C A Schnaitman
Journal:  J Bacteriol       Date:  1970-11       Impact factor: 3.490

8.  Drosophila rhomboid-1 defines a family of putative intramembrane serine proteases.

Authors:  S Urban; J R Lee; M Freeman
Journal:  Cell       Date:  2001-10-19       Impact factor: 41.582

9.  Identification of signal peptide peptidase, a presenilin-type aspartic protease.

Authors:  Andreas Weihofen; Kathleen Binns; Marius K Lemberg; Keith Ashman; Bruno Martoglio
Journal:  Science       Date:  2002-06-21       Impact factor: 47.728

10.  Mitochondrial membrane potential regulates PINK1 import and proteolytic destabilization by PARL.

Authors:  Seok Min Jin; Michael Lazarou; Chunxin Wang; Lesley A Kane; Derek P Narendra; Richard J Youle
Journal:  J Cell Biol       Date:  2010-11-29       Impact factor: 10.539

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  3 in total

1.  Single-Molecule Analyses Reveal Rhomboid Proteins Are Strict and Functional Monomers in the Membrane.

Authors:  Alex J B Kreutzberger; Siniša Urban
Journal:  Biophys J       Date:  2018-10-02       Impact factor: 4.033

2.  Decoding the Functional Evolution of an Intramembrane Protease Superfamily by Statistical Coupling Analysis.

Authors:  Ljubica Mihaljević; Siniša Urban
Journal:  Structure       Date:  2020-08-13       Impact factor: 5.006

3.  Rhomboid distorts lipids to break the viscosity-imposed speed limit of membrane diffusion.

Authors:  Alex J B Kreutzberger; Ming Ji; Siniša Urban; Jesse Aaron; Ljubica Mihaljević
Journal:  Science       Date:  2019-02-01       Impact factor: 47.728

  3 in total

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