Literature DB >> 22987358

Analyzing oligomerization of individual transmembrane helices and of entire membrane proteins in E. coli: A hitchhiker's guide to GALLEX.

Florian Cymer1, Charles R Sanders, Dirk Schneider.   

Abstract

Genetic systems, which allow monitoring interactions of individual transmembrane α-helices within the cytoplasmic membrane of the bacterium Escherichia coli, are now widely used to probe the structural biology and energetics of helix-helix interactions and the consequences of mutations. In contrast to other systems, the GALLEX system allows studying homo- as well as heterooligomerization of individual transmembrane α-helices, and even enables estimation of the energetics of helix-helix interactions within a biological membrane. Given that many polytopic membrane proteins form oligomers within membranes, the GALLEX system represents a unique and powerful approach to monitor formation and stability of oligomeric complexes of polytopic membrane proteins in vivo.

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Year:  2013        PMID: 22987358     DOI: 10.1007/978-1-62703-065-6_16

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  The HIV-1 envelope transmembrane domain binds TLR2 through a distinct dimerization motif and inhibits TLR2-mediated responses.

Authors:  Eliran Moshe Reuven; Mohammad Ali; Etai Rotem; Roland Schwarzer; Roland Schwarzter; Andrea Gramatica; Anthony H Futerman; Yechiel Shai
Journal:  PLoS Pathog       Date:  2014-08-14       Impact factor: 6.823

  1 in total

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