Todokoro K, Kanazawa S, Amanuma H, Ikawa Y
Tsukuba Life Science Center, Institute of Physical and Chemical Research, Ibaraki, Japan.
Biochim Biophys Acta. 1988 Aug 18;943(2):326-30. doi: 10.1016/0005-2736(88)90564-0.
A membrane receptor for erythropoietin was identified in various erythropoietin-unresponsive mouse erythroleukemia cells. Scatchard analyses of the binding of human 125I-labeled erythropoietin to T3C1-2-0, K-1, GM86 and 707 cells showed the presence of a single class of binding sites with apparent Kd values of 0.27-0.78 nM, which are slightly higher than those of erythropoietin-responsive cells. The number of binding sites varied from 110 to 930 per cell. Crosslinking of 125I-erythropoietin to its binding sites with disuccinimidyl suberate revealed the existence of a single binding protein with molecular mass of 63 kDa. No binding sites with higher molecular mass, as observed in erythropoietin-responsive cells, were detected, nor was any specific binding observed to the non-erythroid hematopoietic cell or to the human erythroleukemia cells examined.
在多种对促红细胞生成素无反应的小鼠红白血病细胞中鉴定出了促红细胞生成素的膜受体。对人125I标记的促红细胞生成素与T3C1 - 2 - 0、K - 1、GM86和707细胞结合的Scatchard分析显示存在一类单一的结合位点,其表观解离常数(Kd)值为0.27 - 0.78 nM,略高于促红细胞生成素反应性细胞的Kd值。每个细胞的结合位点数在110至930之间变化。用辛二酸二琥珀酰亚胺酯将125I - 促红细胞生成素与其结合位点交联,揭示存在一种分子量为63 kDa的单一结合蛋白。未检测到在促红细胞生成素反应性细胞中观察到的更高分子量的结合位点,也未观察到与非红系造血细胞或所检测的人红白血病细胞的任何特异性结合。