Carraway K L, Liu Y, Puett D, Carraway K L, Carraway C A
FASEB J. 1987 Jul;1(1):46-50. doi: 10.1096/fasebj.1.1.3301497.
Microvilli isolated from 13762 mammary ascites tumor cells contain a major calcium-sensitive protein (AMV-p35) that can be isolated with microvillar microfilament cores prepared by Triton X-100 extraction in the presence but not absence of calcium. AMV-p35 can be readily purified from ethylene glycol bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid extracts of the microfilament cores by chromatography on an anion exchange column, to which it does not bind. Immunoblot analysis indicates that AMV-p35 is related to calpactin I, the pp60src tyrosine kinase substrate. In the presence of calcium, AMV-p35 binds approximately 4 mol of chlorpromazine per mole of protein in a binding process showing apparent positive cooperativity, similar to calmodulin; however, in contrast to calmodulin, AMV-p35 also binds phenothiazine in the absence of calcium.
从13762乳腺腹水肿瘤细胞中分离出的微绒毛含有一种主要的钙敏感蛋白(AMV-p35),该蛋白可通过在有钙而非无钙的情况下用Triton X-100提取制备的微绒毛微丝核心进行分离。AMV-p35可以很容易地从微丝核心的乙二醇双(β-氨基乙醚)-N,N,N',N'-四乙酸提取物中通过阴离子交换柱色谱法纯化,它不与该柱结合。免疫印迹分析表明,AMV-p35与钙结合蛋白I(pp60src酪氨酸激酶底物)相关。在有钙的情况下,AMV-p35在一个显示出明显正协同性的结合过程中,每摩尔蛋白质结合约4摩尔氯丙嗪,类似于钙调蛋白;然而,与钙调蛋白不同的是,AMV-p35在无钙的情况下也能结合吩噻嗪。