1xop

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Revision as of 03:28, 25 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1xop" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xop" /> '''NMR structure of G1V mutant of influenza hem...)
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1xop

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NMR structure of G1V mutant of influenza hemagglutinin fusion peptide in DPC micelles at pH 5

OverviewOverview

Influenza virus hemagglutinin (HA)-mediated membrane fusion is initiated, by a conformational change that releases a V-shaped hydrophobic fusion, domain, the fusion peptide, into the lipid bilayer of the target membrane., The most N-terminal residue of this domain, a glycine, is highly conserved, and is particularly critical for HA function; G1S and G1V mutant HAs cause, hemifusion and abolish fusion, respectively. We have determined the atomic, resolution structures of the G1S and G1V mutant fusion domains in membrane, environments. G1S forms a V with a disrupted "glycine edge" on its, N-terminal arm and G1V adopts a slightly tilted linear helical structure, in membranes. Abolishment of the kink in G1V results in reduced, hydrophobic penetration of the lipid bilayer and an increased propensity, to form beta-structures at the membrane surface. These results underline, the functional importance of the kink in the fusion peptide and suggest a, structural role for the N-terminal glycine ridge in viral membrane fusion.

About this StructureAbout this Structure

1XOP is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

ReferenceReference

Membrane structures of the hemifusion-inducing fusion peptide mutant G1S and the fusion-blocking mutant G1V of influenza virus hemagglutinin suggest a mechanism for pore opening in membrane fusion., Li Y, Han X, Lai AL, Bushweller JH, Cafiso DS, Tamm LK, J Virol. 2005 Sep;79(18):12065-76. PMID:16140782

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