Margossian S S, Slayter H S
Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York.
J Muscle Res Cell Motil. 1987 Oct;8(5):437-47. doi: 10.1007/BF01578433.
Structural properties of dog cardiac myosin and the influence of the regulatory light chain (LC2) on the shape of myosin heads were investigated by electron microscopy. LC2 was reversibly removed using a neutral protease from myopathic hamsters (Margossian, J. Biol. Chem. 260 (1985) 13747-54). The distribution of myosin head length centred around 17 nm with the mean length being 18.9 nm. Statistical analysis suggested that myosin heads became more globular upon removal of LC2. No extensive aggregation of myosin could be detected after LC2 was dissociated, either by sedimentation velocity or by gels run under non-denaturing conditions. The centre-to-centre distance between heads remained constant at about 21 nm, regardless of the presence or absence of LC2. The distribution of length of the globular region reveals two peaks at 7.5 and 9.5 nm, suggesting an extended and a shorter configuration of this region. The decrease in mass at the head/tail junction upon LC2 removal suggests that it is the binding site for the regulatory light chains. A bend at 57 nm from the head/tail joint was sometimes noticed, corresponding to the myosin hinge region. In high resolution micrographs individual particles revealed invaginations along the contours of the head, possibly delineating the boundaries of structural domains within the head. The conformation of arrowheads in actin decorated with either subfragment 1 (S1) or heavy meromyosin (HMM) was investigated in the presence and absence of LC2.
通过电子显微镜研究了犬心肌肌球蛋白的结构特性以及调节轻链(LC2)对肌球蛋白头部形状的影响。使用中性蛋白酶从患有肌病的仓鼠中可逆地去除LC2(Margossian,《生物化学杂志》260(1985)13747 - 54)。肌球蛋白头部长度分布以17 nm为中心,平均长度为18.9 nm。统计分析表明,去除LC2后肌球蛋白头部变得更加呈球状。在LC2解离后,无论是通过沉降速度还是在非变性条件下进行凝胶电泳,均未检测到肌球蛋白的广泛聚集。无论有无LC2,头部之间的中心距均保持在约21 nm不变。球状区域长度的分布在7.5和9.5 nm处显示出两个峰值,表明该区域存在伸展和较短的构型。去除LC2后头部/尾部连接处质量的降低表明它是调节轻链的结合位点。有时会在距头部/尾部连接处57 nm处注意到一个弯曲,对应于肌球蛋白铰链区。在有和没有LC2的情况下,研究了用亚片段1(S1)或重酶解肌球蛋白(HMM)装饰的肌动蛋白中箭头的构象。