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重组可溶性小鼠D因子/白血病抑制因子受体分析

Analysis of recombinant soluble mouse D-factor/LIF receptor.

作者信息

Tomida M

机构信息

Department of Chemotherapy, Saitama Cancer Center Research Institute.

出版信息

J Biochem. 1995 Jun;117(6):1228-31. doi: 10.1093/oxfordjournals.jbchem.a124848.

Abstract

The recombinant soluble mouse D-factor/LIF receptor (sD-factor-R) was expressed in COS-7 cells. Scatchard analysis of the bindings of mouse 125I-D-factor and human 125I-D-factor to the sD-factor-R indicated dissociation constants (Kd) of 12 and 0.267 nM, respectively, which were comparable to those of the binding protein in mouse serum. The apparent molecular masses of the sD-factor-R and human D-factor observed by gel filtration chromatography were 150 and 50 kDa, respectively. The size of the sD-factor-R.human D-factor complex was approximately 200 kDa, indicating that D-factor forms a 1:1 complex with the sD-factor-R. The sD-factor-R inhibited the induction of differentiation of mouse myeloid leukemic M1 cells by mouse D-factor by blocking the binding of this factor to the cells.

摘要

重组可溶性小鼠D因子/LIF受体(sD因子-R)在COS-7细胞中表达。对小鼠125I-D因子和人125I-D因子与sD因子-R结合的Scatchard分析表明,解离常数(Kd)分别为12和0.267 nM,这与小鼠血清中结合蛋白的解离常数相当。通过凝胶过滤色谱法观察到的sD因子-R和人D因子的表观分子量分别为150 kDa和50 kDa。sD因子-R.人D因子复合物的大小约为200 kDa,表明D因子与sD因子-R形成1:1复合物。sD因子-R通过阻断该因子与细胞的结合,抑制了小鼠D因子对小鼠髓系白血病M1细胞的分化诱导。

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