EmrE, a model for studying evolution and mechanism of ion-coupled transporters

Shimon Schuldiner*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

131 Scopus citations

Abstract

EmrE is a small (110 residues) SMR transporter from Escherichia coli that extrudes positively charged aromatic drugs in exchange for two protons, thus rendering bacteria resistant to a variety of toxic compounds. Due to its size, stability and retention of its function upon solubilization in detergent, EmrE provides a unique experimental paradigm for the biochemical and biophysical studies of membrane based ion-coupled transporters. In addition, EmrE has been in center stage in the past two years because it provides also a paradigm for the study of the evolution of membrane proteins. Controversy around this topic is still going on and some novel concepts are surfacing that may contribute to our understanding of evolution of topology of membrane proteins. Furthermore, based on the findings that the cell multidrug transporters interact functionally we introduce the concept of a cell Resistosome.

Original languageEnglish
Pages (from-to)748-762
Number of pages15
JournalBiochimica et Biophysica Acta - Proteins and Proteomics
Volume1794
Issue number5
DOIs
StatePublished - May 2009

Keywords

  • Ion-coupled transport
  • Membrane protein
  • Multidrug resistance
  • Oligomeric structure
  • Resistosome
  • SMR transporter
  • Topology

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