2akr: Difference between revisions

New page: left|200px<br /><applet load="2akr" size="450" color="white" frame="true" align="right" spinBox="true" caption="2akr, resolution 1.90Å" /> '''Structural basis of ...
 
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[[Image:2akr.gif|left|200px]]<br /><applet load="2akr" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2akr.gif|left|200px]]<br /><applet load="2akr" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2akr, resolution 1.90&Aring;" />
caption="2akr, resolution 1.90&Aring;" />
'''Structural basis of sulfatide presentation by mouse CD1d'''<br />
'''Structural basis of sulfatide presentation by mouse CD1d'''<br />


==Overview==
==Overview==
Sulfatide derived from the myelin stimulates a distinct population of, CD1d-restricted natural killer T (NKT) cells. Cis-tetracosenoyl sulfatide, is one of the immunodominant species in myelin as identified by, proliferation, cytokine secretion, and CD1d tetramer staining. The crystal, structure of mouse CD1d in complex with cis-tetracosenoyl sulfatide at 1.9, A resolution reveals that the longer cis-tetracosenoyl fatty acid chain, fully occupies the A' pocket of the CD1d binding groove, whereas the, sphingosine chain fills up the F' pocket. A precise hydrogen bond network, in the center of the binding groove orients and positions the ceramide, backbone for insertion of the lipid tails in their respective pockets. The, 3'-sulfated galactose headgroup is highly exposed for presentation to the, T cell receptor and projects up and away from the binding pocket due to, its beta linkage, compared with the more intimate binding of the, alpha-glactosyl ceramide headgroup to CD1d. These structure and binding, data on sulfatide presentation by CD1d have important implications for the, design of therapeutics that target T cells reactive for myelin glycolipids, in autoimmune diseases of the central nervous system.
Sulfatide derived from the myelin stimulates a distinct population of CD1d-restricted natural killer T (NKT) cells. Cis-tetracosenoyl sulfatide is one of the immunodominant species in myelin as identified by proliferation, cytokine secretion, and CD1d tetramer staining. The crystal structure of mouse CD1d in complex with cis-tetracosenoyl sulfatide at 1.9 A resolution reveals that the longer cis-tetracosenoyl fatty acid chain fully occupies the A' pocket of the CD1d binding groove, whereas the sphingosine chain fills up the F' pocket. A precise hydrogen bond network in the center of the binding groove orients and positions the ceramide backbone for insertion of the lipid tails in their respective pockets. The 3'-sulfated galactose headgroup is highly exposed for presentation to the T cell receptor and projects up and away from the binding pocket due to its beta linkage, compared with the more intimate binding of the alpha-glactosyl ceramide headgroup to CD1d. These structure and binding data on sulfatide presentation by CD1d have important implications for the design of therapeutics that target T cells reactive for myelin glycolipids in autoimmune diseases of the central nervous system.


==About this Structure==
==About this Structure==
2AKR is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with NAG and CIS as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2AKR OCA].  
2AKR is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with <scene name='pdbligand=NAG:'>NAG</scene> and <scene name='pdbligand=CIS:'>CIS</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2AKR OCA].  


==Reference==
==Reference==
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[[Category: Maricic, I.]]
[[Category: Maricic, I.]]
[[Category: Roy, K.]]
[[Category: Roy, K.]]
[[Category: Wilson, I.A.]]
[[Category: Wilson, I A.]]
[[Category: Wong, C.H.]]
[[Category: Wong, C H.]]
[[Category: Wu, D.]]
[[Category: Wu, D.]]
[[Category: Zajonc, D.M.]]
[[Category: Zajonc, D M.]]
[[Category: CIS]]
[[Category: CIS]]
[[Category: NAG]]
[[Category: NAG]]
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[[Category: tcr]]
[[Category: tcr]]


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