Max-Planck-Institut für Biochemie, D-8033 Martinsried, FRG.
EMBO J. 1982;1(8):1017-22. doi: 10.1002/j.1460-2075.1982.tb01287.x.
The binding sites of five monoclonal antibodies against myosin of Dictyostelium discoideum have been mapped. These antibodies bind to the tail region of the myosin molecule. By rotary shadowing, images of myosin-antibody complexes were obtained in which the mean distance of the midpoint of an antibody molecule from the myosin heads was localized with a precision better than 2 nm (90% confidence limit). Other quantitative data extracted from electron micrographs provided information on the stoichiometry of antibody-myosin interaction. Certain antibodies interacted with myosin molecules only at a ratio of 1:1. Other antibodies formed complexes of two molecules bound to homologous sites on a double-stranded myosin tail. Affinities were estimated and the abilities of different antibodies to cross-connect two myosin molecules were evaluated.
已经定位了针对盘基网柄菌肌球蛋白的 5 种单克隆抗体的结合位点。这些抗体结合在肌球蛋白分子的尾部区域。通过旋转阴影技术,获得了肌球蛋白-抗体复合物的图像,其中抗体分子中点到肌球蛋白头部的平均距离的定位精度优于 2nm(90%置信限)。从电子显微镜照片中提取的其他定量数据提供了关于抗体-肌球蛋白相互作用的化学计量学信息。某些抗体与肌球蛋白分子的相互作用比例仅为 1:1。其他抗体形成了与双链肌球蛋白尾部上的同源位点结合的两个分子的复合物。估计了亲和力,并评估了不同抗体将两个肌球蛋白分子交叉连接的能力。