Yamada T, Sagara J, Shimizu H
J Biochem. 1978 May;83(5):1367-74. doi: 10.1093/oxfordjournals.jbchem.a132045.
A "ghost" myofibril (myosin-extracted myofibril) Sephadex conjugate which specifically binds myosin, HMM and S-1 in the absence of Mg-ATP or Mg-PP can be prepared in a few days by conjugating "ghost" myofibrils to Sephadex beads. Binding ability is retained for over a month. It is used, therefore, for actin-affinity chromatography of myosin and its active fragments. It is under debate whether the two heads of the myosin molecule are functionally identical. Recently several reports have indicated that S-1 could be separated into two kinds of S-1, one giving the initial burst of phosphate and the other not, by assuming a difference in the affinity of the two kinds of S-1 to F-actin. Attempts are reported here to obtain these two components of S-1 separately by using the "ghost" myofibril Sephadex conjugate column. The method of S-1 separation reported by Shibata-Sekiya and Tonomura ((1976) J. Biochem, 80, 1371-1380), which used S-1 treated with CMB, was applied to the "ghost" myofibril Sephadex conjugate column. This resulted in the successful separation of S-1 modified with CMB giving no initial burst of phosphate and unmodified S-1 giving the initial burst of phosphate. A separation method based essentially on the principle employed by Taniguichi and Tawada ((1976) J. Biochem. 80, 853-860) gave an unsuccessful result.
一种“幽灵”肌原纤维(肌球蛋白抽提肌原纤维)葡聚糖凝胶偶联物可在数天内通过将“幽灵”肌原纤维与葡聚糖凝胶珠偶联而制备,该偶联物在不存在Mg-ATP或Mg-PP的情况下能特异性结合肌球蛋白、重酶解肌球蛋白(HMM)和S-1。其结合能力可保持一个多月。因此,它用于肌球蛋白及其活性片段的肌动蛋白亲和层析。关于肌球蛋白分子的两个头部在功能上是否相同仍存在争议。最近有几份报告表明,通过假定两种S-1对F-肌动蛋白的亲和力不同,S-1可分为两种,一种能产生最初的磷酸盐释放爆发,另一种则不能。本文报道了尝试通过使用“幽灵”肌原纤维葡聚糖凝胶偶联柱分别获得S-1的这两种组分。柴田-关谷和户村((1976年)《生物化学杂志》,80卷,1371 - 1380页)报道的使用经对氯汞苯甲酸(CMB)处理的S-1的S-1分离方法被应用于“幽灵”肌原纤维葡聚糖凝胶偶联柱。这成功地分离出了经CMB修饰且不产生最初磷酸盐释放爆发的S-1和产生最初磷酸盐释放爆发的未修饰S-1。一种基本上基于谷口和田田((1976年)《生物化学杂志》,80卷,853 - 860页)所采用原理的分离方法得到了不成功的结果。