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1sje
From Proteopedia
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| - | [[Image:1sje.gif|left|200px]]<br /> | + | [[Image:1sje.gif|left|200px]]<br /><applet load="1sje" size="350" color="white" frame="true" align="right" spinBox="true" |
| - | <applet load="1sje" size=" | + | |
caption="1sje, resolution 2.45Å" /> | caption="1sje, resolution 2.45Å" /> | ||
'''HLA-DR1 complexed with a 16 residue HIV capsid peptide bound in a hairpin conformation'''<br /> | '''HLA-DR1 complexed with a 16 residue HIV capsid peptide bound in a hairpin conformation'''<br /> | ||
==Overview== | ==Overview== | ||
| - | T cells generally recognize peptide antigens bound to MHC proteins through | + | T cells generally recognize peptide antigens bound to MHC proteins through contacts with residues found within or immediately flanking the seven- to nine-residue sequence accommodated in the MHC peptide-binding groove. However, some T cells require peptide residues outside this region for activation, the structural basis for which is unknown. Here, we have investigated a HIV Gag-specific T cell clone that requires an unusually long peptide antigen for activation. The crystal structure of a minimally antigenic 16-mer bound to HLA-DR1 shows that the peptide C-terminal region bends sharply into a hairpin turn as it exits the binding site, orienting peptide residues outside the MHC-binding region in position to interact with a T cell receptor. Peptide truncation and substitution studies show that both the hairpin turn and the extreme C-terminal residues are required for T cell activation. These results demonstrate a previously unrecognized mode of MHC-peptide-T cell receptor interaction. |
==About this Structure== | ==About this Structure== | ||
| - | 1SJE is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Full crystallographic information is available from [http:// | + | 1SJE is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SJE OCA]. |
==Reference== | ==Reference== | ||
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[[Category: Protein complex]] | [[Category: Protein complex]] | ||
[[Category: Staphylococcus aureus]] | [[Category: Staphylococcus aureus]] | ||
| - | [[Category: Norris, P | + | [[Category: Norris, P J.]] |
| - | [[Category: Stern, L | + | [[Category: Stern, L J.]] |
[[Category: Strug, I.]] | [[Category: Strug, I.]] | ||
| - | [[Category: Walker, B | + | [[Category: Walker, B D.]] |
[[Category: Zavala-Ruiz, Z.]] | [[Category: Zavala-Ruiz, Z.]] | ||
[[Category: antigen]] | [[Category: antigen]] | ||
| Line 30: | Line 29: | ||
[[Category: superantigen]] | [[Category: superantigen]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:02:05 2008'' |
Revision as of 13:02, 21 February 2008
|
HLA-DR1 complexed with a 16 residue HIV capsid peptide bound in a hairpin conformation
Overview
T cells generally recognize peptide antigens bound to MHC proteins through contacts with residues found within or immediately flanking the seven- to nine-residue sequence accommodated in the MHC peptide-binding groove. However, some T cells require peptide residues outside this region for activation, the structural basis for which is unknown. Here, we have investigated a HIV Gag-specific T cell clone that requires an unusually long peptide antigen for activation. The crystal structure of a minimally antigenic 16-mer bound to HLA-DR1 shows that the peptide C-terminal region bends sharply into a hairpin turn as it exits the binding site, orienting peptide residues outside the MHC-binding region in position to interact with a T cell receptor. Peptide truncation and substitution studies show that both the hairpin turn and the extreme C-terminal residues are required for T cell activation. These results demonstrate a previously unrecognized mode of MHC-peptide-T cell receptor interaction.
About this Structure
1SJE is a Protein complex structure of sequences from Homo sapiens and Staphylococcus aureus. Full crystallographic information is available from OCA.
Reference
A hairpin turn in a class II MHC-bound peptide orients residues outside the binding groove for T cell recognition., Zavala-Ruiz Z, Strug I, Walker BD, Norris PJ, Stern LJ, Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13279-84. Epub 2004 Aug 26. PMID:15331779
Page seeded by OCA on Thu Feb 21 15:02:05 2008
