The EGF-like domain of chick acetylcholine receptor-inducing activity (ARIA) contains its full biological activity

被引:12
作者
Yang, JF [1 ]
Ng, YP [1 ]
Pun, S [1 ]
Ip, NY [1 ]
Tsim, KWK [1 ]
机构
[1] HONG KONG UNIV SCI & TECHNOL,DEPT BIOL,HONG KONG,HONG KONG
关键词
acetylcholine receptor; extracellular matrix; neuromuscular junction; synapse formation;
D O I
10.1016/S0014-5793(97)00044-6
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
Acetylcholine receptor-inducing activity (ARIA) is a glycoprotein initially purified from chick brain based on its ability to increase the synthesis of acetylcholine receptor (AChR) on cultured myotubes. cDNA encoding ARIA contains different domains and the functions of each domain in ARIA activity are not known, We used molecular genetic methods to construct a chimeric fusion protein, designated ARIA(S136-K205)-Fc, that contained the leader sequence, the EGF-like domain of chick ARIA (S-136 to K-205) and the Fc region of human immunoglobulin, The ARIA(S136)-(K205)-Fc cDNA was transfected into HEK 293 cells and stable cell lines secreting soluble ARIA(S136-K205)-FC were obtained, The secreted ARIA(S136-K205)-Fc has a molecular mass of similar to 60 kDa and can be purified by protein G chromatography. The purified ARIA(S136-K205)-FC retained its full biological activity of chick ARIA that included: (i) induction of tyrosine phosphorylation of erbB 3 receptor in C2C12 myotubes; and (ii) similar to 12-fold stimulation of AChR alpha-subunit mRNA synthesis when applied onto cultured chick myotubes. This Fc-tagged ARIA could be rapidly purified and provides a very useful ligand for identifying its true receptor(s) on muscle cell surface. (C) 1997 Federation of European Biochemical Societies.
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页码:163 / 167
页数:5
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