Fenner C, Valentine R, Mason D T, Wikman-Coffelt J
Prep Biochem. 1975;5(3):189-97. doi: 10.1080/00327487508061571.
A new procedure was developed to purify tropomyosin. The procedure was an adaptation of that described for purification of myosin. By eliminating troponin before precipitating with (NH4)2 SO4, it was possible to obtain pure tropomyosin from the same preparation from which myosin was purified. When tropomyosin was subjected to isoelectrofocusing two tropomyosins were present, having similar isoelectric points of pH 5.4 and 5.6; two tropomyosin subunits were resolved in the presence of 6 M urea. The two subunits had very similar isoelectric points, pH 4.7 and 5.0. According to Ouchterlony analyses the tropomyosins from canine skeletal and cardiac tissue were immunologically identical when incubated with goat gammaG antitropomyosin (cardiac).
开发了一种纯化原肌球蛋白的新方法。该方法是对用于纯化肌球蛋白的方法的改进。通过在用硫酸铵沉淀之前去除肌钙蛋白,可以从纯化肌球蛋白的同一制剂中获得纯原肌球蛋白。当对原肌球蛋白进行等电聚焦时,出现了两种原肌球蛋白,其等电点相似,分别为pH 5.4和5.6;在6M尿素存在下可分辨出两个原肌球蛋白亚基。这两个亚基的等电点非常相似,分别为pH 4.7和5.0。根据双向免疫扩散分析,当与山羊γG抗原肌球蛋白(心脏)一起孵育时,犬骨骼肌和心脏组织中的原肌球蛋白在免疫上是相同的。