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The role of trimerization in the osmoregulated betaine transporter BetP.
- Source :
-
EMBO reports [EMBO Rep] 2011 Jun 17; Vol. 12 (8), pp. 804-10. Date of Electronic Publication: 2011 Jun 17. - Publication Year :
- 2011
-
Abstract
- The osmoregulated betaine transporter BetP is a stable trimer. Structural studies have shown that individual protomers can adopt distinct transport conformations, implying a functional role for the trimeric state in transport, although the role of trimerization in regulation is not yet understood. We designed putative monomeric mutants by molecular-dynamics simulations and in silico alanine-scanning mutagenesis. Several mutants including BetP-W101A/T351A were monomeric in detergent as well as in the membrane, as shown by blue native gel electrophoresis, crosslinking and electron microscopy. This monomeric form retains the ability to accumulate betaine, but is no longer regulated by hyperosmotic shock.
- Subjects :
- Bacterial Proteins genetics
Biological Transport
Carrier Proteins genetics
Escherichia coli metabolism
GABA Plasma Membrane Transport Proteins
Models, Molecular
Mutation
Protein Multimerization
Protein Subunits chemistry
Proteolipids metabolism
Structure-Activity Relationship
Symporters
Tomography, X-Ray Computed methods
Water-Electrolyte Balance
Bacterial Proteins chemistry
Bacterial Proteins metabolism
Betaine metabolism
Carrier Proteins chemistry
Carrier Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1469-3178
- Volume :
- 12
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- EMBO reports
- Publication Type :
- Academic Journal
- Accession number :
- 21681199
- Full Text :
- https://doi.org/10.1038/embor.2011.102