Literature DB >> 11969415

Structure of the transition state of gating in the acetylcholine receptor channel pore: a phi-value analysis.

Gisela D Cymes1, Claudio Grosman, Anthony Auerbach.   

Abstract

The gating mechanism of the acetylcholine receptor channel (AChR) was investigated by using rate equilibrium linear free energy relationships (LFERs) to probe the transition state between the closed and open conformations. The properties of the transition state of gating in the second transmembrane segment (M2) of the delta subunit, one of the five homologous pore-lining segments, was measured on a residue-by-residue basis. Series of point mutations were engineered at individual positions of this domain, and the corresponding constructs were characterized electrophysiologically, at the single-channel level. Fully liganded AChR opening and closing rate constants were estimated, and Phi-values (which are a measure of the extent of the conformational change realized at the transition state) were calculated for each reaction series as the slope of the Brønsted relationship (log rate constant versus log equilibrium constant). Our results indicate that, at the transition state of gating, the extracellular half of deltaM2 partly resembles the open state (Phi-values between 0.24 and 0.38) while the intracellular half completely resembles the closed state (Phi-values between -0.18 and 0.03), with a break point near the middle of the M2 segment. This suggests that during gating the two halves of deltaM2 move asynchronously, with the rearrangement of the extracellular portion preceding (following) that of the intracellular part of deltaM2 during opening (closing). This particular sequence of molecular events indicates that the gating conformational change, which starts at the extracellular acetylcholine-binding sites (when opening), does not propagate exclusively along the primary sequence of the protein. In addition, our data are consistent with the deltaM2 segment bending or swiveling around its central residues during gating. We also elaborate on unsettled aspects of the analysis such as the accuracy of two-point LFERs, the physical interpretation of fractional Phi-values, and the existence of single versus parallel transition states for the gating reaction.

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Year:  2002        PMID: 11969415      PMCID: PMC6442467          DOI: 10.1021/bi011864f

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  48 in total

1.  Free-energy landscapes of ion-channel gating are malleable: changes in the number of bound ligands are accompanied by changes in the location of the transition state in acetylcholine-receptor channels.

Authors:  Claudio Grosman
Journal:  Biochemistry       Date:  2003-12-23       Impact factor: 3.162

2.  Phi-value analysis and the nature of protein-folding transition states.

Authors:  Alan R Fersht; Satoshi Sato
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-18       Impact factor: 11.205

3.  Mutations that stabilize the open state of the Erwinia chrisanthemi ligand-gated ion channel fail to change the conformation of the pore domain in crystals.

Authors:  Giovanni Gonzalez-Gutierrez; Tiit Lukk; Vinayak Agarwal; David Papke; Satish K Nair; Claudio Grosman
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-02       Impact factor: 11.205

4.  Mapping the sequence of conformational changes underlying selectivity filter gating in the K(v)11.1 potassium channel.

Authors:  David T Wang; Adam P Hill; Stefan A Mann; Peter S Tan; Jamie I Vandenberg
Journal:  Nat Struct Mol Biol       Date:  2010-12-19       Impact factor: 15.369

5.  Subunit symmetry at the extracellular domain-transmembrane domain interface in acetylcholine receptor channel gating.

Authors:  Iva Bruhova; Anthony Auerbach
Journal:  J Biol Chem       Date:  2010-09-23       Impact factor: 5.157

6.  A speed limit for conformational change of an allosteric membrane protein.

Authors:  Sudha Chakrapani; Anthony Auerbach
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-23       Impact factor: 11.205

7.  Gating of acetylcholine receptor channels: brownian motion across a broad transition state.

Authors:  Anthony Auerbach
Journal:  Proc Natl Acad Sci U S A       Date:  2005-01-21       Impact factor: 11.205

8.  Dynamics of the acetylcholine receptor pore at the gating transition state.

Authors:  Ananya Mitra; Gisela D Cymes; Anthony Auerbach
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-10       Impact factor: 11.205

9.  Maximum likelihood estimation of ion channel kinetics from macroscopic currents.

Authors:  Lorin S Milescu; Gustav Akk; Frederick Sachs
Journal:  Biophys J       Date:  2005-01-28       Impact factor: 4.033

10.  A gating mechanism proposed from a simulation of a human alpha7 nicotinic acetylcholine receptor.

Authors:  Richard J Law; Richard H Henchman; J Andrew McCammon
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-27       Impact factor: 11.205

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