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PMID: 16239220 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

The osmotic activation of transporter ProP is tuned by both its C-terminal coiled-coil and osmotically induced changes in phospholipid composition.

The Journal of biological chemistry ·Vol. 280 ·No. 50 ·2005-12-16 ·Pages 41387-94

Tsatskis Y, Khambati J, Dobson M, Bogdanov M, Dowhan W, Wood JM

Abstract

Transporter ProP of Escherichia coli (ProPEc) senses extracellular osmolality and mediates osmoprotectant uptake when it is rising or high. A replica of the ProPEc C terminus (Asp468-Arg497) forms an intermolecular alpha-helical coiled-coil. This structure is implicated in the osmoregulation of intact ProPEc, in vivo. Like that from Corynebacterium glutamicum (ProPCg), the ProP orthologue from Agrobacterium tumefaciens (ProPAt) sensed and responded to extracellular osmolality after expression in E. coli. The osmotic activation profiles of all three orthologues depended on the osmolality of the bacterial growth medium, the osmolality required for activation rising as the growth osmolality approached 0.7 mol/kg. Thus, each could undergo osmotic adaptation. The proportion of cardiolipin in a polar lipid extract from E. coli increased with extracellular osmolality so that the osmolality activating ProPEc was a direct function of membrane cardiolipin content. Group A ProP orthologues (ProPEc, ProPAt) share the C-terminal coiled-coil domain and were activated at low osmolalities. Like variant ProPEc-R488I, in which the C-terminal coiled-coil is disrupted, ProPEc derivatives that lack the coiled-coil and Group B orthologue ProPCg required a higher osmolality to activate. The amplitude of ProPEc activation was reduced 10-fold in its deletion derivatives. The coiled-coil structure is not essential for osmotic activation of ProP per se. However, it tunes Group A orthologues to osmoregulate over a low osmolality range. Coiled-coil lesions may impair both coiled-coil formation and interaction of ProPEc with amplifier protein ProQ. Cardiolipin may contribute to ProP adaptation by altering bulk membrane properties or by acting as a ProP ligand.

MeSH Terms
Amino Acid Sequence Arginine/chemistry Aspartic Acid/chemistry Binding Sites Biological Transport Blotting, Western Cardiolipins/metabolism Cell Membrane/metabolism Codon, Terminator Culture Media/metabolism,pharmacology Dose-Response Relationship, Drug Escherichia coli/metabolism Escherichia coli Proteins/metabolism,physiology Gene Deletion Ions Ligands Lipids/chemistry Magnetic Resonance Spectroscopy Membrane Transport Proteins/metabolism Models, Chemical Molecular Sequence Data Mutagenesis, Site-Directed Osmolar Concentration Osmosis Phospholipids/chemistry,metabolism Plasmids/metabolism Potassium/chemistry Protein Binding Protein Conformation Protein Structure, Secondary Protein Structure, Tertiary Receptors, Scavenger/metabolism Symporters/metabolism,physiology
Chemicals
Cardiolipins Codon, Terminator Culture Media Escherichia coli Proteins Ions Ligands Lipids Membrane Transport Proteins Phospholipids ProP protein, E coli Receptors, Scavenger Symporters Aspartic Acid Arginine Potassium
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Tsatskis Yonit
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.
Khambati Jumana
Dobson Martina
Bogdanov Mikhail
Dowhan William
Wood Janet M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2005-12-16
Epub
2005-00-20
Pages
41387-94
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · R37 GM20487 · United States
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