1egj: Difference between revisions

New page: left|200px<br /> <applet load="1egj" size="450" color="white" frame="true" align="right" spinBox="true" caption="1egj, resolution 2.8Å" /> '''DOMAIN 4 OF THE BETA...
 
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[[Image:1egj.gif|left|200px]]<br />
[[Image:1egj.gif|left|200px]]<br /><applet load="1egj" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1egj" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1egj, resolution 2.8&Aring;" />
caption="1egj, resolution 2.8&Aring;" />
'''DOMAIN 4 OF THE BETA COMMON CHAIN IN COMPLEX WITH AN ANTIBODY'''<br />
'''DOMAIN 4 OF THE BETA COMMON CHAIN IN COMPLEX WITH AN ANTIBODY'''<br />


==Overview==
==Overview==
Heterodimeric cytokine receptors generally consist of a major, cytokine-binding subunit and a signaling subunit. The latter can transduce, signals by more than 1 cytokine, as exemplified by the, granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-2, (IL-2), and IL-6 receptor systems. However, often the signaling subunits, in isolation are unable to bind cytokines, a fact that has made it more, difficult to obtain structural definition of their ligand-binding sites., This report details the crystal structure of the ligand-binding domain of, the GM-CSF/IL-3/IL-5 receptor beta-chain (beta(c)) signaling subunit in, complex with the Fab fragment of the antagonistic monoclonal antibody, BION-1. This is the first single antagonist of all 3 known, eosinophil-producing cytokines, and it is therefore capable of regulating, eosinophil-related diseases such as asthma. The structure reveals a, fibronectin type III domain, and the antagonist-binding site involves, major contributions from the loop between the B and C strands and overlaps, the cytokine-binding site. Furthermore, tyrosine(421) (Tyr(421)), a key, residue involved in receptor activation, lies in the neighboring loop, between the F and G strands, although it is not immediately adjacent to, the cytokine-binding residues in the B-C loop. Interestingly, functional, experiments using receptors mutated across these loops demonstrate that, they are cooperatively involved in full receptor activation. The, experiments, however, reveal subtle differences between the B-C loop and, Tyr(421), which is suggestive of distinct functional roles. The, elucidation of the structure of the ligand-binding domain of beta(c) also, suggests how different cytokines recognize a single receptor subunit, which may have implications for homologous receptor systems. (Blood., 2000;95:2491-2498)
Heterodimeric cytokine receptors generally consist of a major cytokine-binding subunit and a signaling subunit. The latter can transduce signals by more than 1 cytokine, as exemplified by the granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-2 (IL-2), and IL-6 receptor systems. However, often the signaling subunits in isolation are unable to bind cytokines, a fact that has made it more difficult to obtain structural definition of their ligand-binding sites. This report details the crystal structure of the ligand-binding domain of the GM-CSF/IL-3/IL-5 receptor beta-chain (beta(c)) signaling subunit in complex with the Fab fragment of the antagonistic monoclonal antibody, BION-1. This is the first single antagonist of all 3 known eosinophil-producing cytokines, and it is therefore capable of regulating eosinophil-related diseases such as asthma. The structure reveals a fibronectin type III domain, and the antagonist-binding site involves major contributions from the loop between the B and C strands and overlaps the cytokine-binding site. Furthermore, tyrosine(421) (Tyr(421)), a key residue involved in receptor activation, lies in the neighboring loop between the F and G strands, although it is not immediately adjacent to the cytokine-binding residues in the B-C loop. Interestingly, functional experiments using receptors mutated across these loops demonstrate that they are cooperatively involved in full receptor activation. The experiments, however, reveal subtle differences between the B-C loop and Tyr(421), which is suggestive of distinct functional roles. The elucidation of the structure of the ligand-binding domain of beta(c) also suggests how different cytokines recognize a single receptor subunit, which may have implications for homologous receptor systems. (Blood. 2000;95:2491-2498)


==About this Structure==
==About this Structure==
1EGJ 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/Mus_musculus Mus musculus] with NAG as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1EGJ OCA].  
1EGJ 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/Mus_musculus Mus musculus] with <scene name='pdbligand=NAG:'>NAG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EGJ OCA].  


==Reference==
==Reference==
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[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Bagley, C.J.]]
[[Category: Bagley, C J.]]
[[Category: Hercus, T.R.]]
[[Category: Hercus, T R.]]
[[Category: Lopez, A.F.]]
[[Category: Lopez, A F.]]
[[Category: McClure, B.J.]]
[[Category: McClure, B J.]]
[[Category: McKinstry, W.J.]]
[[Category: McKinstry, W J.]]
[[Category: Parker, M.W.]]
[[Category: Parker, M W.]]
[[Category: Rossjohn, J.]]
[[Category: Rossjohn, J.]]
[[Category: Woodcock, J.M.]]
[[Category: Woodcock, J M.]]
[[Category: NAG]]
[[Category: NAG]]
[[Category: cytokine receptor complexed to an antibody]]
[[Category: cytokine receptor complexed to an antibody]]


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