Document Detail


Induction of substrate specificity shifts by placement of alanine insertions within the consensus amphipathic region of the Escherichia coli GABA (gamma-aminobutyric acid) transporter encoded by gabP.
MedLine Citation:
PMID:  12956623     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Escherichia coli GABA (gamma-aminobutyric acid) permease GabP is a prototypical APC (amine/polyamine/choline) super-family transporter that has a CAR (consensus amphipathic region) containing multiple specificity determinants, ostensibly organized on two helical surfaces, one hydrophobic [SHS (sensitive hydrophobic surface)] and the other hydrophilic [SPS (sensitive polar surface)]. To gauge the functional effects of placing alanine insertions at close intervals across the entire GabP CAR, 64 insertion variants were constructed. Insertions, particularly those in the SHS and the SPS, were highly detrimental to steady-state [(3)H]GABA accumulation. TSR (transport specificity ratio) analysis, employing [(3)H]nipecotic acid and [(14)C]GABA, showed that certain alanine insertions were associated with a specificity shift (i.e. a change in k (cat)/ K (m)). An insertion (INS Ala-269) located N-terminal to the SHS increased specificity for [(3)H]nipecotic acid relative to [(14)C]GABA, whereas an insertion (INS Ala-321) located C-terminal to the SPS had the opposite effect. Overall, the results are consistent with a working hypothesis that the GabP CAR contains extensive functional surfaces that may be manipulated by insertion mutagenesis to alter the specificity ( k (cat)/ K (m)) phenotype. The thermodynamic basis of TSR analysis provides generality, suggesting that amino acid insertions could affect specificity in many other transporters, particularly those such as the E. coli phenylalanine permease PheP [Pi, Chow and Pittard (2002) J. Bacteriol. 184, 5842-5847] that have a functionally significant CAR-like domain.
Authors:
Steven C King; Liaoyuan A Hu; Amy Pugh
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Biochemical journal     Volume:  376     ISSN:  1470-8728     ISO Abbreviation:  Biochem. J.     Publication Date:  2003 Dec 
Date Detail:
Created Date:  2003-12-05     Completed Date:  2004-01-12     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  2984726R     Medline TA:  Biochem J     Country:  England    
Other Details:
Languages:  eng     Pagination:  645-53     Citation Subset:  IM    
Affiliation:
Department of Integrated Biosciences, Oregon Health & Science University, Portland, OR 97239-3097, USA. kingst@ohsu.edu
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MeSH Terms
Descriptor/Qualifier:
Alanine / genetics
Amino Acid Sequence
Biological Transport / drug effects
Carrier Proteins / chemistry*,  genetics,  metabolism*
Consensus Sequence
Escherichia coli Proteins / chemistry*,  genetics,  metabolism*
GABA Plasma Membrane Transport Proteins
Genes, Reporter
Hydrophobicity
Immunoblotting
Membrane Proteins / chemistry*,  genetics,  metabolism*
Membrane Transport Proteins*
Models, Molecular
Molecular Sequence Data
Mutagenesis, Insertional
Organic Anion Transporters / chemistry*,  genetics,  metabolism*
Protein Structure, Secondary
Substrate Specificity
beta-Galactosidase / genetics,  metabolism
gamma-Aminobutyric Acid / metabolism
Grant Support
ID/Acronym/Agency:
NS38226/NS/NINDS NIH HHS
Chemical
Reg. No./Substance:
0/Carrier Proteins; 0/Escherichia coli Proteins; 0/GABA Plasma Membrane Transport Proteins; 0/Membrane Proteins; 0/Membrane Transport Proteins; 0/Organic Anion Transporters; 0/gabP protein, E coli; 56-12-2/gamma-Aminobutyric Acid; 56-41-7/Alanine; EC 3.2.1.23/beta-Galactosidase
Comments/Corrections

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