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4NQV

Crystal Structure of HLA A*0101 in complex with NP44, an 9-mer influenza epitope

Summary for 4NQV
Entry DOI10.2210/pdb4nqv/pdb
Related4NQX
DescriptorHLA class I histocompatibility antigen, A-1 alpha chain, Beta-2-microglobulin, Nucleoprotein, ... (4 entities in total)
Functional Keywordsimmune system, hla presenting h7n9 viral epitope, t cell receptor, immune system-viral protein complex, immune system/viral protein
Biological sourceHomo sapiens (human)
More
Cellular locationMembrane; Single-pass type I membrane protein: P30443
Secreted: P61769
Total number of polymer chains18
Total formula weight267531.13
Authors
Rossjohn, J.,Gras, S. (deposition date: 2013-11-25, release date: 2013-12-25, Last modification date: 2024-11-06)
Primary citationQuinones-Parra, S.,Grant, E.,Loh, L.,Nguyen, T.H.,Campbell, K.A.,Tong, S.Y.,Miller, A.,Doherty, P.C.,Vijaykrishna, D.,Rossjohn, J.,Gras, S.,Kedzierska, K.
Preexisting CD8+ T-cell immunity to the H7N9 influenza A virus varies across ethnicities.
Proc.Natl.Acad.Sci.USA, 111:1049-1054, 2014
Cited by
PubMed Abstract: The absence of preexisting neutralizing antibodies specific for the novel A (H7N9) influenza virus indicates a lack of prior human exposure. As influenza A virus-specific CD8(+) T lymphocytes (CTLs) can be broadly cross-reactive, we tested whether immunogenic peptides derived from H7N9 might be recognized by memory CTLs established following infection with other influenza strains. Probing across multiple ethnicities, we identified 32 conserved epitopes derived from the nucleoprotein (NP) and matrix-1 (M1) proteins. These NP and M1 peptides are presented by HLAs prevalent in 16-57% of individuals. Remarkably, some HLA alleles (A*0201, A*0301, B*5701, B*1801, and B*0801) elicit robust CTL responses against any human influenza A virus, including H7N9, whereas ethnicities where HLA-A*0101, A*6801, B*1501, and A*2402 are prominent, show limited CTL response profiles. By this criterion, some groups, especially the Alaskan and Australian Indigenous peoples, would be particularly vulnerable to H7N9 infection. This dissection of CTL-mediated immunity to H7N9 thus suggests strategies for both vaccine delivery and development.
PubMed: 24395804
DOI: 10.1073/pnas.1322229111
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.39 Å)
Structure validation

227111

数据于2024-11-06公开中

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