1a3r: Difference between revisions

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[[Image:1a3r.gif|left|200px]]
[[Image:1a3r.gif|left|200px]]


{{Structure
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'''FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170)'''
'''FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170)'''
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[[Category: Fita, I.]]
[[Category: Fita, I.]]
[[Category: Tormo, J.]]
[[Category: Tormo, J.]]
[[Category: antibody]]
[[Category: Antibody]]
[[Category: complex (immunoglobulin/viral peptide)]]
[[Category: Continuous epitope]]
[[Category: continuous epitope]]
[[Category: Immunoglobulin]]
[[Category: immunoglobulin]]
[[Category: Neutralization]]
[[Category: neutralization]]
[[Category: Rhinovirus]]
[[Category: rhinovirus]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May  2 09:46:06 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 18:32:36 2008''

Revision as of 09:46, 2 May 2008

File:1a3r.gif

Template:STRUCTURE 1a3r

FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170)


OverviewOverview

The three-dimensional structure of the complex between the Fab fragment of an anti-human rhinovirus neutralizing antibody (8F5) and a cross-reactive synthetic peptide from the viral capsid protein VP2 has been determined at 2.5 A resolution by crystallographic methods. The refinement is presently at an R factor of 0.18 and the antigen-binding site and viral peptide are well defined. The peptide antigen adopts a compact fold by two tight turns and interacts through hydrogen bonds, some with ionic character, and van der Waals contacts with antibody residues from the six hypervariable loops as well as several framework amino acids. The conformation adopted by the peptide is closely related to the corresponding region of the viral protein VP2 on the surface of human rhinovirus 1A whose three-dimensional structure is known. Implications for the cross-reactivity between peptides and the viral capsid are discussed. The peptide-antibody interactions, together with the analysis of mutant viruses that escape neutralization by 8F5 suggest two different mechanisms for viral escape. The comparison between the complexed and uncomplexed antibody structures shows important conformational rearrangements, especially in the hypervariable loops of the heavy chain. Thus, it constitutes a clear example of the 'induced fit' molecular recognition mechanism.

About this StructureAbout this Structure

1A3R is a Protein complex structure of sequences from Human rhinovirus 2 and Mus musculus. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of a human rhinovirus neutralizing antibody complexed with a peptide derived from viral capsid protein VP2., Tormo J, Blaas D, Parry NR, Rowlands D, Stuart D, Fita I, EMBO J. 1994 May 15;13(10):2247-56. PMID:8194515 Page seeded by OCA on Fri May 2 09:46:06 2008

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