2akr

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(New page: 200px<br /><applet load="2akr" size="450" color="white" frame="true" align="right" spinBox="true" caption="2akr, resolution 1.90&Aring;" /> '''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"
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[[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==
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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.
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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==
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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].
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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.]]
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[[Category: Wilson, I.A.]]
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[[Category: Wilson, I A.]]
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[[Category: Wong, C.H.]]
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[[Category: Wong, C H.]]
[[Category: Wu, D.]]
[[Category: Wu, D.]]
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[[Category: Zajonc, D.M.]]
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[[Category: Zajonc, D M.]]
[[Category: CIS]]
[[Category: CIS]]
[[Category: NAG]]
[[Category: NAG]]
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[[Category: tcr]]
[[Category: tcr]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 08:11:34 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:28:23 2008''

Revision as of 14:28, 21 February 2008


2akr, resolution 1.90Å

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Structural basis of sulfatide presentation by mouse CD1d

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.

About this Structure

2AKR is a Protein complex structure of sequences from Mus musculus with and as ligands. Full crystallographic information is available from OCA.

Reference

Structural basis for CD1d presentation of a sulfatide derived from myelin and its implications for autoimmunity., Zajonc DM, Maricic I, Wu D, Halder R, Roy K, Wong CH, Kumar V, Wilson IA, J Exp Med. 2005 Dec 5;202(11):1517-26. Epub 2005 Nov 28. PMID:16314439

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