Dos Remedios C G, Cooke R
Biochim Biophys Acta. 1984 Jul 31;788(2):193-205. doi: 10.1016/0167-4838(84)90262-0.
The structural relationship between F-actin filaments and the biologically active fragments of myosin (either as myosin subfragment-1 or heavy meromyosin) has been investigated using the technique of fluorescence energy transfer. Donor and acceptor probes were used to obtain the following inter- and intramolecular distances. Energy transfer was measured: (1) from the SH1 groups of the myosin 'heads' to the nucleotide sites of F-actin (in the absence of free nucleotide); (2) from the SH1 groups of myosin to multiple probes on the surface of the actin filament; (3) from the nucleotide-binding sites of F-actin to the ATPase sites of myosin; (4) from the ATPase sites of myosin to the nucleotide-binding sites of F-actin; (5) from the SH1 sites of myosin to the nucleotide-binding sites of F-actin; and (6) from the Cys-373 residues of F-actin to the nucleotide binding sites of F-actin. We observed very little energy transfer between the probes on actin and the probes on myosin (10% or less) and we observed a large transfer between the actin Cys-373 and the actin nucleotide. These data strongly suggest that both the SH1 moiety and the ATPase site of myosin are located more than 6 nm from the actin sites. When these distances are combined with similar measurements by other authors and inserted into the most recent three-dimensional reconstruction of electron micrographs of the acto-subfragment-1 complex, it is apparent that the SH1 and the ATPase sites on myosin are not located adjacent to actin and are most probably located in the half of the myosin head that is distal from actin in the actomyosin complex.
利用荧光能量转移技术研究了F-肌动蛋白丝与肌球蛋白生物活性片段(肌球蛋白亚片段-1或重酶解肌球蛋白)之间的结构关系。使用供体和受体探针来获得以下分子间和分子内距离。测量了能量转移:(1)从肌球蛋白“头部”的SH1基团到F-肌动蛋白的核苷酸位点(在没有游离核苷酸的情况下);(2)从肌球蛋白的SH1基团到肌动蛋白丝表面的多个探针;(3)从F-肌动蛋白的核苷酸结合位点到肌球蛋白的ATP酶位点;(4)从肌球蛋白的ATP酶位点到F-肌动蛋白的核苷酸结合位点;(5)从肌球蛋白的SH1位点到F-肌动蛋白的核苷酸结合位点;以及(6)从F-肌动蛋白的Cys-373残基到F-肌动蛋白的核苷酸结合位点。我们观察到肌动蛋白上的探针与肌球蛋白上的探针之间的能量转移非常少(10%或更少),并且观察到肌动蛋白Cys-373与肌动蛋白核苷酸之间有大量转移。这些数据强烈表明,肌球蛋白的SH1部分和ATP酶位点都位于距肌动蛋白位点超过6 nm的位置。当将这些距离与其他作者的类似测量结果相结合,并插入到肌动蛋白-亚片段-1复合物电子显微镜最新的三维重建中时,很明显肌球蛋白上的SH1和ATP酶位点并不位于肌动蛋白附近,很可能位于肌动球蛋白复合物中肌球蛋白头部远离肌动蛋白的那一半。