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1q1j

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(New page: 200px<br /> <applet load="1q1j" size="450" color="white" frame="true" align="right" spinBox="true" caption="1q1j, resolution 2.50&Aring;" /> '''Crystal Structure A...)
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<applet load="1q1j" size="450" color="white" frame="true" align="right" spinBox="true"
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'''Crystal Structure Analysis of anti-HIV-1 Fab 447-52D in complex with V3 peptide'''<br />
'''Crystal Structure Analysis of anti-HIV-1 Fab 447-52D in complex with V3 peptide'''<br />
==Overview==
==Overview==
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447-52D is a human monoclonal antibody isolated from a heterohybridoma, derived from an HIV-1-infected individual. This antibody recognizes the, hypervariable gp120 V3 loop, and neutralizes both X4 and R5 primary, isolates, making it one of the most effective anti-V3 antibodies, characterized to date. The crystal structure of the 447-52D Fab in complex, with a 16-mer V3 peptide at 2.5 A resolution reveals that the peptide beta, hairpin forms a three-stranded mixed beta sheet with complementarity, determining region (CDR) H3, with most of the V3 side chains exposed to, solvent. Sequence specificity is conferred through interaction of the, type-II turn (residues GPGR) at the apex of the V3 hairpin with the base, of CDR H3. This novel mode of peptide-antibody recognition enables the, antibody to bind to many different V3 sequences where only the GPxR core, epitope is absolutely required.
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447-52D is a human monoclonal antibody isolated from a heterohybridoma derived from an HIV-1-infected individual. This antibody recognizes the hypervariable gp120 V3 loop, and neutralizes both X4 and R5 primary isolates, making it one of the most effective anti-V3 antibodies characterized to date. The crystal structure of the 447-52D Fab in complex with a 16-mer V3 peptide at 2.5 A resolution reveals that the peptide beta hairpin forms a three-stranded mixed beta sheet with complementarity determining region (CDR) H3, with most of the V3 side chains exposed to solvent. Sequence specificity is conferred through interaction of the type-II turn (residues GPGR) at the apex of the V3 hairpin with the base of CDR H3. This novel mode of peptide-antibody recognition enables the antibody to bind to many different V3 sequences where only the GPxR core epitope is absolutely required.
==About this Structure==
==About this Structure==
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1Q1J is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Q1J OCA].
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1Q1J is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Q1J OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Gorny, M.K.]]
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[[Category: Gorny, M K.]]
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[[Category: Stanfield, R.L.]]
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[[Category: Stanfield, R L.]]
[[Category: Williams, C.]]
[[Category: Williams, C.]]
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[[Category: Wilson, I.A.]]
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[[Category: Wilson, I A.]]
[[Category: Zolla-Pazner, S.]]
[[Category: Zolla-Pazner, S.]]
[[Category: fab-peptide complex]]
[[Category: fab-peptide complex]]
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[[Category: v3 loop]]
[[Category: v3 loop]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Thu Nov 8 14:23:33 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:34:55 2008''

Revision as of 12:35, 21 February 2008


1q1j, resolution 2.50Å

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Crystal Structure Analysis of anti-HIV-1 Fab 447-52D in complex with V3 peptide

Overview

447-52D is a human monoclonal antibody isolated from a heterohybridoma derived from an HIV-1-infected individual. This antibody recognizes the hypervariable gp120 V3 loop, and neutralizes both X4 and R5 primary isolates, making it one of the most effective anti-V3 antibodies characterized to date. The crystal structure of the 447-52D Fab in complex with a 16-mer V3 peptide at 2.5 A resolution reveals that the peptide beta hairpin forms a three-stranded mixed beta sheet with complementarity determining region (CDR) H3, with most of the V3 side chains exposed to solvent. Sequence specificity is conferred through interaction of the type-II turn (residues GPGR) at the apex of the V3 hairpin with the base of CDR H3. This novel mode of peptide-antibody recognition enables the antibody to bind to many different V3 sequences where only the GPxR core epitope is absolutely required.

About this Structure

1Q1J is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural rationale for the broad neutralization of HIV-1 by human monoclonal antibody 447-52D., Stanfield RL, Gorny MK, Williams C, Zolla-Pazner S, Wilson IA, Structure. 2004 Feb;12(2):193-204. PMID:14962380

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