1s9w

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[[Image:1s9w.jpg|left|200px]]
[[Image:1s9w.jpg|left|200px]]
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{{Structure
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The line below this paragraph, containing "STRUCTURE_1s9w", creates the "Structure Box" on the page.
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{{STRUCTURE_1s9w| PDB=1s9w | SCENE= }}
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|RELATEDENTRY=[[1s9x|1S9X]], [[1s9y|1S9Y]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1s9w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1s9w OCA], [http://www.ebi.ac.uk/pdbsum/1s9w PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1s9w RCSB]</span>
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'''Crystal Structure Analysis of NY-ESO-1 epitope, SLLMWITQC, in complex with HLA-A2'''
'''Crystal Structure Analysis of NY-ESO-1 epitope, SLLMWITQC, in complex with HLA-A2'''
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[[Category: Rossjohn, J.]]
[[Category: Rossjohn, J.]]
[[Category: Webb, A I.]]
[[Category: Webb, A I.]]
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[[Category: immune system]]
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[[Category: Immune system]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 08:27:56 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:39:15 2008''
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Revision as of 05:27, 3 May 2008

Template:STRUCTURE 1s9w

Crystal Structure Analysis of NY-ESO-1 epitope, SLLMWITQC, in complex with HLA-A2


Overview

NY-ESO-1, a commonly expressed tumor antigen of the cancer-testis family, is expressed by a wide range of tumors but not found in normal adult somatic tissue, making it an ideal cancer vaccine candidate. Peptides derived from NY-ESO-1 have shown preclinical and clinical trial promise; however, biochemical features of these peptides have complicated their formulation and led to heterogeneous immune responses. We have taken a rational approach to engineer an HLA A2-restricted NY-ESO-1-derived T cell epitope with improved formulation and immunogenicity to the wild type peptide. To accomplish this, we have solved the x-ray crystallographic structures of HLA A2 complexed to NY-ESO (157-165) and two analogues of this peptide in which the C-terminal cysteine residue has been substituted to alanine or serine. Substitution of cysteine by serine maintained peptide conformation yet reduced complex stability, resulting in poor cytotoxic T lymphocyte recognition. Conversely, substitution with alanine maintained complex stability and cytotoxic T lymphocyte recognition. Based on the structures of the three HLA A2 complexes, we incorporated 2-aminoisobutyric acid, an isostereomer of cysteine, into the epitope. This analogue is impervious to oxidative damage, cysteinylation, and dimerization of the peptide epitope upon formulation that is characteristic of the wild type peptide. Therefore, this approach has yielded a potential therapeutic molecule that satiates the hydrophobic F pocket of HLA A2 and exhibited superior immunogenicity relative to the wild type peptide.

About this Structure

1S9W is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Functional and structural characteristics of NY-ESO-1-related HLA A2-restricted epitopes and the design of a novel immunogenic analogue., Webb AI, Dunstone MA, Chen W, Aguilar MI, Chen Q, Jackson H, Chang L, Kjer-Nielsen L, Beddoe T, McCluskey J, Rossjohn J, Purcell AW, J Biol Chem. 2004 May 28;279(22):23438-46. Epub 2004 Mar 5. PMID:15004033 Page seeded by OCA on Sat May 3 08:27:56 2008

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