2hp4: Difference between revisions

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[[Image:2hp4.jpg|left|200px]]
{{Seed}}
[[Image:2hp4.png|left|200px]]


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{{STRUCTURE_2hp4|  PDB=2hp4  |  SCENE=  }}  
{{STRUCTURE_2hp4|  PDB=2hp4  |  SCENE=  }}  


'''Computational design and crystal structure of an enhanced affinity mutant human CD8-alpha-alpha co-receptor'''
===Computational design and crystal structure of an enhanced affinity mutant human CD8-alpha-alpha co-receptor===




==Overview==
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Human CD8 is a T cell coreceptor, which binds to pHLA I and plays a pivotal role in the activation of cytotoxic T lymphocytes. Soluble recombinant CD8 alphaalpha has been shown to antagonize T cell activation, both in vitro and in vivo. However, because of a very low affinity for pHLA I, high concentrations of soluble CD8 alphaalpha are required for efficient inhibition. Based upon our knowledge of the wild-type CD8/pHLA I structure, we have designed and produced a mutated form of soluble CD8 alphaalpha that binds to pHLA I with approximately fourfold higher affinity. We have characterized the binding of the high affinity CD8 mutant using surface plasmon resonance and determined its structure at 2.1 A resolution using X-ray crystallography. The analysis of this structure suggests that the higher affinity is achieved by providing a larger side chain that allows for an optimal contact to be made between the HLA alpha3 loop and the mutated CDR-like loops of CD8.
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{{ABSTRACT_PUBMED_17243170}}


==About this Structure==
==About this Structure==
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[[Category: Protein engineering]]
[[Category: Protein engineering]]
[[Category: Soluble protein]]
[[Category: Soluble protein]]
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