Literature DB >> 1381444

Structure of an isolated gramicidin A double helical species by high-resolution nuclear magnetic resonance.

S M Pascal1, T A Cross.   

Abstract

A conformational species of gramicidin A has been isolated in dioxane by high pressure liquid chromatography and characterized by circular dichroism and two-dimensional proton nuclear magnetic resonance. Double-quantum filtered two-dimensional correlation spectroscopy, two-dimensional homonuclear Hartman Hahn spectroscopy and two-dimensional nuclear Overhauser effect spectra at 500 MHz were used to obtain virtually complete proton assignments and produce 192 distance constraints. Protocols to determine the state of aggregation, monomer-specific assignment of nuclear Overhauser enhancement values, hydrogen bonding pattern and helix handedness are described. A distance geometry/simulated annealing routine was used to generate well-defined backbone and side-chain structures. The species isolated is a right-handed intertwined double helix, with approximately 5.7 residues per turn. Unique values for helical dimensions are also specified.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1381444     DOI: 10.1016/0022-2836(92)91055-t

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  15 in total

1.  Validation of the single-stranded channel conformation of gramicidin A by solid-state NMR.

Authors:  F Kovacs; J Quine; T A Cross
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

2.  Solvent effects on the conformation of the transmembrane peptide gramicidin A: insights from electrospray ionization mass spectrometry.

Authors:  M Bouchard; D R Benjamin; P Tito; C V Robinson; C M Dobson
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

3.  Electrospray ionization-mass spectrometry and tandem mass spectrometry reveal self-association and metal-ion binding of hydrophobic peptides: a study of the gramicidin dimer.

Authors:  Raghu K Chitta; Michael L Gross
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

4.  High-resolution structure and dynamic implications for a double-helical gramicidin A conformer.

Authors:  S M Pascal; T A Cross
Journal:  J Biomol NMR       Date:  1993-09       Impact factor: 2.835

5.  Conformational trapping in a membrane environment: a regulatory mechanism for protein activity?

Authors:  S Arumugam; S Pascal; C L North; W Hu; K C Lee; M Cotten; R R Ketchem; F Xu; M Brenneman; F Kovacs; F Tian; A Wang; S Huo; T A Cross
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-11       Impact factor: 11.205

6.  Protein stability and conformational rearrangements in lipid bilayers: linear gramicidin, a model system.

Authors:  M Cotten; F Xu; T A Cross
Journal:  Biophys J       Date:  1997-08       Impact factor: 4.033

7.  High-speed magic angle spinning solid-state 1H nuclear magnetic resonance study of the conformation of gramicidin A in lipid bilayers.

Authors:  M Bouchard; J H Davis; M Auger
Journal:  Biophys J       Date:  1995-11       Impact factor: 4.033

8.  Water: foldase activity in catalyzing polypeptide conformational rearrangements.

Authors:  F Xu; T A Cross
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

9.  Structural restraints and heterogeneous orientation of the gramicidin A channel closed state in lipid bilayers.

Authors:  Y Mo; T A Cross; W Nerdal
Journal:  Biophys J       Date:  2004-05       Impact factor: 4.033

10.  High resolution 1H nuclear magnetic resonance of a transmembrane peptide.

Authors:  J H Davis; M Auger; R S Hodges
Journal:  Biophys J       Date:  1995-11       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.