Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain.

The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Abstract Text:

    albert y lauAlbert Y Lau, roux Roux,albert y lauAlbert Y Lau, roux Roux,

    Ionotropic glutamate receptors are ligand-gated transmembrane ion channels activated by the binding of glutamate. The free energy landscapes governing the opening/closing of the GluR2 S1S2 ligand-binding domain in the apo, DNQX-, and glutamate-bound forms are computed by using all-atom molecular dynamics simulations with explicit solvent, in conjunction with an umbrella sampling strategy. The apo S1S2 easily accesses low-energy conformations that are more open than observed in X-ray crystal structures. A free energy of 9-12 kcal/mol becomes available upon glutamate binding for driving conformational changes in S1S2 associated with receptor activation. Small-angle X-ray scattering profiles calculated from computed ensemble averages agree better with experimental results than profiles calculated from static X-ray crystal structures. Water molecules in the cleft may contribute to stabilizing the apo S1S2 in open conformations. Free energy landscapes were also computed for the glutamate-bound T686A and T686S S1S2 mutants, and the results elaborate on findings from experimental functional studies.

    The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Publishing Authors By Initials

    ay lauAY Lau,b rouxB Roux,ay lauAY Lau,b rouxB Roux,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Structure (London, England : 1993)

    VOLUME: 15

    Page Numbers: 1203-14

    Journal Abbreviation: Structure

    ISSN: 0969-2126

    DAY: 16

    MONTH: Oct

    YEAR: 2007

    The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101087697

    The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Keywords Mesh Terms:

    KEYWORDS:

    MESH TERMS:

    Chemical & Substance for Abstract: The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain. Information

    Substance Name:

    Registry Number:

    Grant and Affiliation Information for The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain.

    AFFILIATION: Institute for Molecular Pediatric Sciences, Department of Biochemistry and Molecular Biology, Ellen and Melvin Gordon Center for Integrative Science, The University of Chicago, 929 East 57(th) Street, Chicago, IL 60637, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: GM 62342

    ACRONYM: GM

    MEDLINETA: Structure

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    The free energy landscapes governing conformational changes in a glutamate receptor ligand-binding domain Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News