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在低浓度镁离子存在的情况下,磷酸化肌胃肌球蛋白的肌动蛋白激活的ATP酶活性对钙离子和原肌球蛋白的依赖性。

Dependence on Ca2+ and tropomyosin of the actin-activated ATPase activity of phosphorylated gizzard myosin in the presence of low concentrations of Mg2+.

作者信息

Nag S, Seidel J C

出版信息

J Biol Chem. 1983 May 25;258(10):6444-9.

PMID:6222043
Abstract

Ca2+ and tropomyosin are required for activation of ATPase activity of phosphorylated gizzard myosin by gizzard actin at less than 1 mM Mg2+, relatively low Ca2+ concentrations (1 microM), producing half-maximal activation. At higher concentrations, Mg2+ will replace Ca2+, 4 mM Mg2+ increasing activity to the same extent as does Ca2+ and abolishing the Ca2+ dependence. Above about 1 mM Mg2+, tropomyosin is no longer required for activation by actin, activity being dependent on Ca2+ between 1 and 4 mM Mg2+, but independent of [Ca2+] above 4 mM Mg2+. Phosphorylation of the 20,000-Da light chain of gizzard myosin is required for activation of ATPase activity by actin from chicken gizzard or rabbit skeletal muscle at all concentrations of Mg2+ employed. The effect of adding or removing Ca2+ is fully reversible and cannot be attributed either to irreversible inactivation of actin or myosin or to dephosphorylation. After preincubating in the absence of Ca2+, activity is restored either by adding micromolar concentrations of this cation or by raising the concentration of Mg2+ to 8 mM. Similarly, the inhibition found in the absence of tropomyosin is fully reversed by subsequent addition of this protein. Replacing gizzard actin with skeletal actin alters the pattern of activation by Ca2+ at concentrations of Mg2+ less than 1 mM. Full activation is obtained with or without Ca2+ in the presence of tropomyosin, while in its absence Ca2+ is required but produces only partial activation. Without tropomyosin, the range of Mg2+ concentrations over which activity is Ca2+-dependent is restricted to lower values with skeletal than with gizzard actin. The activity of skeletal muscle myosin is activated by the gizzard actin-tropomyosin complex without Ca2+, although Ca2+ slightly increases activity. The Ca2+ sensitivity of reconstituted gizzard actomyosin is partially retained by hybrid actomyosin containing gizzard myosin and skeletal actin, but less Ca2+ dependence is retained in the hybrid containing skeletal myosin and gizzard actin.

摘要

在镁离子浓度低于1 mM、钙离子浓度相对较低(1 microM)时,钙离子和原肌球蛋白是砂囊肌动蛋白激活磷酸化砂囊肌球蛋白ATP酶活性所必需的,此时可产生半数最大激活。在较高浓度下,镁离子会取代钙离子,4 mM镁离子使活性增加的程度与钙离子相同,并消除了对钙离子的依赖性。在约1 mM镁离子以上,原肌球蛋白不再是肌动蛋白激活所必需的,活性在1至4 mM镁离子之间依赖于钙离子,但在4 mM镁离子以上则与[钙离子]无关。在所有使用的镁离子浓度下,砂囊肌球蛋白20,000道尔顿轻链的磷酸化是鸡砂囊或兔骨骼肌肌动蛋白激活ATP酶活性所必需的。添加或去除钙离子的作用是完全可逆的,既不能归因于肌动蛋白或肌球蛋白的不可逆失活,也不能归因于去磷酸化。在无钙离子的情况下预孵育后,通过添加微摩尔浓度的该阳离子或将镁离子浓度提高到8 mM,活性得以恢复。同样,在随后添加该蛋白后,在无原肌球蛋白时发现的抑制作用会完全逆转。用骨骼肌肌动蛋白取代砂囊肌动蛋白会改变在镁离子浓度低于1 mM时钙离子的激活模式。在有原肌球蛋白存在的情况下,无论有无钙离子均可获得完全激活,而在其不存在时则需要钙离子,但仅产生部分激活。在无原肌球蛋白时,与砂囊肌动蛋白相比,骨骼肌肌动蛋白活性依赖钙离子的镁离子浓度范围限制在较低值。骨骼肌肌球蛋白的活性在无钙离子的情况下被砂囊肌动蛋白 - 原肌球蛋白复合物激活,尽管钙离子会轻微增加活性。含有砂囊肌球蛋白和骨骼肌肌动蛋白的杂交肌动球蛋白部分保留了重组砂囊肌动球蛋白的钙离子敏感性,但含有骨骼肌肌球蛋白和砂囊肌动蛋白的杂交体中对钙离子的依赖性保留较少。

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