Shargill N S, Tatoyan A, el-Refai M F, Pleta M, Chan T M
Biochem Biophys Res Commun. 1986 May 29;137(1):286-94. doi: 10.1016/0006-291x(86)91208-8.
A method has been developed to isolate skeletal muscle plasma membranes from mice in good yield without harsh extraction procedures. The method involves perfusion of mouse hindquarters with a calcium-deficient buffer containing collagenase and hyaluronidase. This is followed by gentle disruption, filtration, and differential centrifugations. The entire procedure takes about six hours and the yield is approximately 4 mg. protein from 10 g. equivalent of hindquarter muscle. The preparation contained predominantly plasma membranes based on specific activities of marker enzymes, electron microscopic data, and specific binding sites for insulin and a -adrenergic ligand. Studies using such preparations from lean, 4-5 week old and 12-20 week old db/db mice showed marked reduction in the phosphorylation of the 95 kDa subunit of the insulin receptor of the obese mice with no change in insulin binding. In addition, there was a progressive reduction in insulin sensitivity in stimulating receptor phosphorylation in the db/db mice.
已经开发出一种方法,可从小鼠中以高产量分离骨骼肌质膜,且无需采用严苛的提取程序。该方法包括用含有胶原酶和透明质酸酶的缺钙缓冲液灌注小鼠后肢。随后进行轻柔破碎、过滤和差速离心。整个过程约需6小时,从10克相当于后肢肌肉的组织中可获得约4毫克蛋白质。基于标记酶的比活性、电子显微镜数据以及胰岛素和α-肾上腺素能配体的特异性结合位点,该制剂主要含有质膜。使用来自4至5周龄和12至20周龄的瘦型及db/db肥胖小鼠的此类制剂进行的研究表明,肥胖小鼠胰岛素受体95 kDa亚基的磷酸化显著降低,而胰岛素结合无变化。此外,在刺激db/db小鼠受体磷酸化方面,胰岛素敏感性逐渐降低。