Tokuda M, Khanna N C, Waisman D M
Department of Medical Biochemistry, University of Calgary, Alberta, Canada.
Biochem J. 1987 Aug 15;246(1):67-74. doi: 10.1042/bj2460067.
A Ca2+-binding protein of molecular mass 48 kDa and named 'CAB-48' has been purified from bovine brain 100,000 g supernatant. About 30 mg of CAB-48 was purified from 1 kg of bovine brain. The protein has been characterized with respect to its physical, chemical and Ca2+-binding properties. It has an apparent molecular mass of 48 kDa by SDS/polyacrylamide-gel-electrophoresis and 75.2 kDa from sedimentation-velocity and Stokes-radius data. The acidic nature of the molecule is suggested by its pI of 4.7. In the presence of 3.0 mM-MgCl2 and 150 mM-KCl, CAB-48 binds 1.0 mol of Ca2+/mol of protein with an apparent Kd of 15 microM. A tyrosine protein kinase partially purified from rat spleen catalysed the incorporation of 0.73 mol of phosphate/mol of CAB-48, and phosphoamino acid analysis revealed that phosphorylation of CAB-48 was specific for tyrosine residues.
一种分子量为48 kDa、名为“CAB - 48”的钙结合蛋白已从牛脑100,000 g上清液中纯化出来。从1千克牛脑中纯化得到了约30毫克的CAB - 48。该蛋白已就其物理、化学和钙结合特性进行了表征。通过SDS /聚丙烯酰胺凝胶电泳,其表观分子量为48 kDa,根据沉降速度和斯托克斯半径数据,其分子量为75.2 kDa。其pI为4.7,表明该分子具有酸性。在存在3.0 mM氯化镁和150 mM氯化钾的情况下,CAB - 48以15 microM的表观解离常数结合1.0摩尔钙离子/摩尔蛋白。从大鼠脾脏中部分纯化的一种酪氨酸蛋白激酶催化了0.73摩尔磷酸盐/摩尔CAB - 48的掺入,磷酸氨基酸分析表明CAB - 48的磷酸化对酪氨酸残基具有特异性。