1sys: Difference between revisions

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[[Image:1sys.gif|left|200px]]
{{Seed}}
[[Image:1sys.png|left|200px]]


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{{STRUCTURE_1sys|  PDB=1sys  |  SCENE=  }}  
{{STRUCTURE_1sys|  PDB=1sys  |  SCENE=  }}  


'''Crystal structure of HLA, B*4403, and peptide EEPTVIKKY'''
===Crystal structure of HLA, B*4403, and peptide EEPTVIKKY===




==Overview==
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HLA class I polymorphism creates diversity in epitope specificity and T cell repertoire. We show that HLA polymorphism also controls the choice of Ag presentation pathway. A single amino acid polymorphism that distinguishes HLA-B*4402 (Asp116) from B*4405 (Tyr116) permits B*4405 to constitutively acquire peptides without any detectable incorporation into the transporter associated with Ag presentation (TAP)-associated peptide loading complex even under conditions of extreme peptide starvation. This mode of peptide capture is less susceptible to viral interference than the conventional loading pathway used by HLA-B*4402 that involves assembly of class I molecules within the peptide loading complex. Thus, B*4402 and B*4405 are at opposite extremes of a natural spectrum in HLA class I dependence on the PLC for Ag presentation. These findings unveil a new layer of MHC polymorphism that affects the generic pathway of Ag loading, revealing an unsuspected evolutionary trade-off in selection for optimal HLA class I loading versus effective pathogen evasion.
The line below this paragraph, {{ABSTRACT_PUBMED_15226359}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_15226359}}


==Disease==
==Disease==
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[[Category: Hla]]
[[Category: Hla]]
[[Category: Mhc]]
[[Category: Mhc]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 09:17:27 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 09:56:40 2008''