Mutational analysis of the CD6 ligand binding domain

被引:17
作者
Skonier, JE
Bodian, DL
Emswiler, J
Bowen, MA
Aruffo, A
Bajorath, J
机构
[1] UNIV WASHINGTON,BMS PRI,SEATTLE,WA 98195
[2] UNIV WASHINGTON,DEPT BIOL STRUCT,SEATTLE,WA 98195
[3] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,SEATTLE,WA 98121
来源
PROTEIN ENGINEERING | 1997年 / 10卷 / 08期
关键词
CD6; mutagenesis; receptor-ligand interaction; scavenger receptor cysteine-rich protein superfamily;
D O I
10.1093/protein/10.8.943
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
CD6 belongs to the scavenger receptor cysteine-rich protein superfamily (SRCRSF), which includes a large number of cell surface proteins, The extracellular region of CD6 is composed of three SRCR domains. The membrane proximal SRCR domain of CD6 (CD6D3) specifically binds activated leukocyte cell adhesion molecule (ALCAM), a cell surface protein which is a member of the immunoglobulin superfamily (IgSF), CD6-ligand interactions have been implicated in immune cell adhesion, T cell maturation and the regulation of T cell activation, We tested 13 CD6D3 mutant proteins for binding to ALCAM and a panel of conformationally sensitive anti-CD6D3 monoclonal antibodies (mAbs), CD6D3 residues were classified according to their importance for structural integrity and ligand binding, The results were analyzed in the light of SRCR domain sequence comparison, A number of residues critical for ligand binding or important for structural integrity cluster in the C-terminal region of CD6D3 which is not conserved in other SRCR proteins.
引用
收藏
页码:943 / 947
页数:5
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