Literature DB >> 9862130

Determination of the equilibrium micelle-inserting position of the fusion peptide of gp41 of human immunodeficiency virus type 1 at amino acid resolution by exchange broadening of amide proton resonances.

D K Chang1, S F Cheng.   

Abstract

The exchange broadening of backbone amide proton resonances of a 23-mer fusion peptide of the transmembrane subunit of HIV-1 envelope glycoprotein gp41, gp41-FP, was investigated at pH 5 and 7 at room temperature in perdeuterated sodium dodecyl sulfate (SDS) micellar solution. Comparison of resonance peaks for these pHs revealed an insignificant change in exchange rate between pH 5 and 7 for amide protons of residues 4 through 14, while the exchange rate increase at neutral pH was more prominent for amide protons of the remaining residues, with peaks from some protons becoming undetectable. The relative insensitivity to pH of the exchange for the amide protons of residues 4 through 14 is attributable to the drastic reduction in [OH-] in the micellar interior, leading to a decreased exchange rate. The A15-G16 segment represents a transition between these two regimes. The data are thus consistent with the notion that the peptide inserts into the hydrophobic core of a membrane-like structure and the A15-G16 dipeptide is located at the micellar-aqueous boundary.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9862130     DOI: 10.1023/a:1008399304450

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  14 in total

1.  Identification of a protein-binding surface by differential amide hydrogen-exchange measurements. Application to Bowman-Birk serine-protease inhibitor.

Authors:  M H Werner; D E Wemmer
Journal:  J Mol Biol       Date:  1992-06-05       Impact factor: 5.469

Review 2.  Viral and cellular membrane fusion proteins.

Authors:  J M White
Journal:  Annu Rev Physiol       Date:  1990       Impact factor: 19.318

3.  The program XEASY for computer-supported NMR spectral analysis of biological macromolecules.

Authors:  C Bartels; T H Xia; M Billeter; P Güntert; K Wüthrich
Journal:  J Biomol NMR       Date:  1995-07       Impact factor: 2.835

4.  Protein folding intermediates: native-state hydrogen exchange.

Authors:  Y Bai; T R Sosnick; L Mayne; S W Englander
Journal:  Science       Date:  1995-07-14       Impact factor: 47.728

5.  An antibody binding site on cytochrome c defined by hydrogen exchange and two-dimensional NMR.

Authors:  Y Paterson; S W Englander; H Roder
Journal:  Science       Date:  1990-08-17       Impact factor: 47.728

6.  The FLG motif in the N-terminal region of glucoprotein 41 of human immunodeficiency virus type 1 adopts a type-I beta turn in aqueous solution and serves as the initiation site for helix formation.

Authors:  D K Chang; W J Chien; S F Cheng
Journal:  Eur J Biochem       Date:  1997-08-01

7.  The amino-terminal fusion domain peptide of human immunodeficiency virus type 1 gp41 inserts into the sodium dodecyl sulfate micelle primarily as a helix with a conserved glycine at the micelle-water interface.

Authors:  D K Chang; S F Cheng; W J Chien
Journal:  J Virol       Date:  1997-09       Impact factor: 5.103

8.  Lipid-anchored influenza hemagglutinin promotes hemifusion, not complete fusion.

Authors:  G W Kemble; T Danieli; J M White
Journal:  Cell       Date:  1994-01-28       Impact factor: 41.582

9.  Hydrogen exchange identifies native-state motional domains important in protein folding.

Authors:  K S Kim; J A Fuchs; C K Woodward
Journal:  Biochemistry       Date:  1993-09-21       Impact factor: 3.162

10.  Gradient-tailored excitation for single-quantum NMR spectroscopy of aqueous solutions.

Authors:  M Piotto; V Saudek; V Sklenár
Journal:  J Biomol NMR       Date:  1992-11       Impact factor: 2.835

View more
  6 in total

1.  Solid-state nuclear magnetic resonance measurements of HIV fusion peptide 13CO to lipid 31P proximities support similar partially inserted membrane locations of the α helical and β sheet peptide structures.

Authors:  Charles M Gabrys; Wei Qiang; Yan Sun; Li Xie; Scott D Schmick; David P Weliky
Journal:  J Phys Chem A       Date:  2013-02-28       Impact factor: 2.781

2.  The conserved glycine-rich segment linking the N-terminal fusion peptide to the coiled coil of human T-cell leukemia virus type 1 transmembrane glycoprotein gp21 is a determinant of membrane fusion function.

Authors:  Kirilee A Wilson; Séverine Bär; Anne L Maerz; Marc Alizon; Pantelis Poumbourios
Journal:  J Virol       Date:  2005-04       Impact factor: 5.103

3.  Oligomeric beta-structure of the membrane-bound HIV-1 fusion peptide formed from soluble monomers.

Authors:  Jun Yang; Mary Prorok; Francis J Castellino; David P Weliky
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

4.  Solid-state nuclear magnetic resonance measurements of HIV fusion peptide to lipid distances reveal the intimate contact of beta strand peptide with membranes and the proximity of the Ala-14-Gly-16 region with lipid headgroups.

Authors:  Wei Qiang; Jun Yang; David P Weliky
Journal:  Biochemistry       Date:  2007-04-07       Impact factor: 3.162

5.  Chemical shift assignment and structural plasticity of a HIV fusion peptide derivative in dodecylphosphocholine micelles.

Authors:  Charles M Gabrys; David P Weliky
Journal:  Biochim Biophys Acta       Date:  2007-08-24

6.  Paramyxovirus F1 protein has two fusion peptides: implications for the mechanism of membrane fusion.

Authors:  S G Peisajovich; O Samuel; Y Shai
Journal:  J Mol Biol       Date:  2000-03-10       Impact factor: 5.469

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.