Nagata K, Nozawa Y
Department of Biochemistry, Gifu University School of Medicine, Japan.
Biochem Biophys Res Commun. 1993 Sep 15;195(2):1081-8. doi: 10.1006/bbrc.1993.2155.
Subcellular fractions were prepared from human platelets by sucrose density gradient centrifugation and the presence of a GTP-binding protein, c25KG, was analyzed by immunoblotting. c25KG was found to be located in plasma membrane and alpha-granule fractions in resting platelets by immunoblot analysis. Disappearance of the protein by the pronase treatment of intact alpha-granules indicated that c25KG is exposed on the cytoplasmic face of the granules. Activation of platelets by thrombin induced the redistribution of c25KG from alpha-granules to plasma membranes. On the other hand, Gi2, which is the main pertussis toxin-substrate in human platelets, was predominantly present in plasma membranes and thrombin-stimulation did not alter its distribution.
通过蔗糖密度梯度离心法从人血小板中制备亚细胞组分,并通过免疫印迹分析一种GTP结合蛋白c25KG的存在情况。通过免疫印迹分析发现,c25KG存在于静息血小板的质膜和α-颗粒组分中。用链霉蛋白酶处理完整的α-颗粒后该蛋白消失,表明c25KG暴露于颗粒的胞质面。凝血酶激活血小板可诱导c25KG从α-颗粒重新分布到质膜。另一方面,人血小板中主要的百日咳毒素底物Gi2主要存在于质膜中,凝血酶刺激不会改变其分布。