The CXCR3 binding chemokine IP-10/CXCL10: Structure and receptor interactions

被引:114
作者
Booth, V
Keizer, DW
Kamphuis, MB
Clark-Lewis, I
Sykes, BD [1 ]
机构
[1] Univ Alberta, Prot Engn Network, Ctr Excellence, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Heritage Med Res Ctr 713, Dept Biochem, Edmonton, AB T6G 2S2, Canada
[3] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Biomed Res Ctr, Vancouver, BC V6T 1Z3, Canada
关键词
D O I
10.1021/bi026020q
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structure of IP-10 was solved by NMR spectroscopy and represents the first structure from the class of agonists toward the receptor CXCR3. CXCR3 binding chemokines are unique in their ability to bind receptors from both the CC and CXC classes of chemokine receptors. An unusual structural feature of IP-10 was identified that may provide the basis for the ability of IP-10 to bind both CXCR3 and CCR3. The surface of IP-10 that interacts with the N-terminus of CXCR3 was defined by monitoring changes in the NMR spectrum of IP-10 upon addition of a CXCR3 N-terminal peptide. These studies indicated that the interaction involves a hydrophobic cleft, formed by the N-loop and 40s-loop region of IP-10, similar to the interaction surface observed for other chemokines such as IL-8. An additional region of interaction was observed that consists of a hydrophobic cleft formed by the N-terminus of IP-10 and 30s-loop of IP-10.
引用
收藏
页码:10418 / 10425
页数:8
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