Muguruma M, Kobayashi K, Fukazawa T, Ohashi K, Maruyama K
J Biochem. 1981 Jun;89(6):1981-4. doi: 10.1093/oxfordjournals.jbchem.a133401.
A new protein with a chain weight of approximately 220,000 was isolated from 0.6 M KI extracts of I-Z-I brushes of rabbit and chicken skeletal muscles, using (NH4)2SO4 precipitation and three column chromatographic procedures in succession. It was only possible to separate the high molecular weight protein from actin and alpha-actinin in the presence of 6 M urea or 0.1% sodium dodecyl sulfate (SDS). The purified protein migrated as a single band on SDS gel electrophoresis. The amino acid composition of the 220,000 dalton protein was distinct from any known proteins found in myofibrils, e.g., alpha-actinin and actin binding protein (ABP; filamin). An indirect immunofluorescence technique revealed that the new protein was exclusively located in the Z lines of myofibrils of chicken breast muscle. There is, however, a possibility that the 220,000 dalton protein is identical with synemin recently isolated from chicken gizzard (Granger, B.L. and Lazarides, E. (1980) Cell 22, 727).
从兔和鸡骨骼肌的I-Z-I刷状缘的0.6M KI提取物中,通过硫酸铵沉淀和连续的三步柱色谱法,分离出一种链重约为220,000的新蛋白质。只有在6M尿素或0.1%十二烷基硫酸钠(SDS)存在的情况下,才有可能将这种高分子量蛋白质与肌动蛋白和α-辅肌动蛋白分离。纯化后的蛋白质在SDS凝胶电泳中迁移为单一的条带。这种220,000道尔顿蛋白质的氨基酸组成与肌原纤维中发现的任何已知蛋白质都不同,例如α-辅肌动蛋白和肌动蛋白结合蛋白(ABP;细丝蛋白)。间接免疫荧光技术显示,这种新蛋白质仅位于鸡胸肌肌原纤维的Z线中。然而,这种220,000道尔顿的蛋白质有可能与最近从鸡砂囊中分离出的伴肌动蛋白相同(格兰杰,B.L.和拉扎里德斯,E.(1980年)《细胞》22卷,第727页)。