Literature DB >> 34395783

Structural Analysis of Target Protein by Substituted Cysteine Accessibility Method.

Tetsuo Cai1, Taisuke Tomita1.   

Abstract

Substituted Cysteine Accessibility Method (SCAM) is a biochemical approach to investigate the water accessibility or the spatial distance of particular cysteine residues substituted in the target protein. Protein topology and structure can be annotated by labeling with methanethiosulfonate reagents that specifically react with the cysteine residues facing the hydrophilic environment, even within the transmembrane domain. Cysteine crosslinking experiments provide us with information about the distance between two cysteine residues. The combination of these methods enables us to obtain information about the structural changes of the target protein. Here, we describe the detailed protocol for structural analysis using SCAM.
Copyright © 2018 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Biotinylation; Crosslinking; Cysteine; Membrane protein; Structural analysis; Substitution; Water accessibility

Year:  2018        PMID: 34395783      PMCID: PMC8328659          DOI: 10.21769/BioProtoc.2470

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  20 in total

1.  Transmembrane protein topology mapping by the substituted cysteine accessibility method (SCAM(TM)): application to lipid-specific membrane protein topogenesis.

Authors:  Mikhail Bogdanov; Wei Zhang; Jun Xie; William Dowhan
Journal:  Methods       Date:  2005-06       Impact factor: 3.608

Review 2.  Cys-scanning mutagenesis: a novel approach to structure function relationships in polytopic membrane proteins.

Authors:  S Frillingos; M Sahin-Tóth; J Wu; H R Kaback
Journal:  FASEB J       Date:  1998-10       Impact factor: 5.191

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Authors:  R P Seal; B H Leighton; S G Amara
Journal:  Methods Enzymol       Date:  1998       Impact factor: 1.600

4.  Probing the Structure and Function Relationships of Presenilin by Substituted-Cysteine Accessibility Method.

Authors:  T Tomita
Journal:  Methods Enzymol       Date:  2016-11-23       Impact factor: 1.600

5.  Cysteine mutants as chemical sensors for ligand-receptor interactions.

Authors:  B Foucaud; P Perret; T Grutter; M Goeldner
Journal:  Trends Pharmacol Sci       Date:  2001-04       Impact factor: 14.819

6.  C5a receptor oligomerization. I. Disulfide trapping reveals oligomers and potential contact surfaces in a G protein-coupled receptor.

Authors:  Jeffery M Klco; Tracey B Lassere; Thomas J Baranski
Journal:  J Biol Chem       Date:  2003-06-30       Impact factor: 5.157

7.  Acetylcholine receptor channel structure probed in cysteine-substitution mutants.

Authors:  M H Akabas; D A Stauffer; M Xu; A Karlin
Journal:  Science       Date:  1992-10-09       Impact factor: 47.728

8.  Membrane topology of a cysteine-less mutant of human P-glycoprotein.

Authors:  T W Loo; D M Clarke
Journal:  J Biol Chem       Date:  1995-01-13       Impact factor: 5.157

9.  The C-terminal PAL motif and transmembrane domain 9 of presenilin 1 are involved in the formation of the catalytic pore of the gamma-secretase.

Authors:  Chihiro Sato; Shizuka Takagi; Taisuke Tomita; Takeshi Iwatsubo
Journal:  J Neurosci       Date:  2008-06-11       Impact factor: 6.167

10.  Conformational Changes in Transmembrane Domain 4 of Presenilin 1 Are Associated with Altered Amyloid-β 42 Production.

Authors:  Aya Tominaga; Tetsuo Cai; Shizuka Takagi-Niidome; Takeshi Iwatsubo; Taisuke Tomita
Journal:  J Neurosci       Date:  2016-01-27       Impact factor: 6.167

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