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一种与微管相关蛋白2(MAP 2)的突出部分结合的蛋白激酶。

A protein kinase bound to the projection portion of MAP 2 (microtubule-associated protein 2).

作者信息

Vallee R B, DiBartolomeis M J, Theurkauf W E

出版信息

J Cell Biol. 1981 Sep;90(3):568-76. doi: 10.1083/jcb.90.3.568.

Abstract

In previous work we have demonstrated that the microtubule-associated protein 2 (MAP 2) molecule consists of two structural parts. One part of the molecule, referred to as the assembly-promoting domain, binds to the microtubule surface and is responsible for promoting microtubule assembly; the other represents a filamentous projection observed on the microtubule surface that may be involved in the interaction of microtubules with other cellular structures. MAP 2 is known to be specifically phosphorylated as the result of a protein kinase activity that is present in microtubule preparations. We have now found that the activity copurifies with the projection portion of MAP 2 itself. Kinase activity coeluted with MAP 2 when microtubule protein was subjected to either gel- filtration chromatography on bio-gel A-15m or ion-exchange chromatography on DEAE- Sephadex. The activity was released from microtubules by mild digestion with chymotrypsin in parallel with the removal by the protease of the MAP 2 projections from the microtubule surface. The association of the activity with the projection was demonstrated directly by gel filtration chromatography of the projections on bio-gel A-15m. Three protein species (M(r) = 39,000, 55,000, and 70,000) cofractionated with MAP 2, and two of these (M(r) = 39,000 and 55,000) may represent the subunits of an associated cyclic AMP- dependent protein kinase. The projection-associated activity was stimulated 10-fold by cyclic AMP and was inhibited more than 95 percent by the cyclic AMP-dependent protein kinase inhibitor from rabbit skeletal muscle. It appeared to represent the only significant activity associated with microtubules, almost no activity being found with tubulin, other MAPs, or the assembly-promoting domain of MAP 2, and was estimated to account for 7-22 percent of the total brain cytosolic protein kinase activity. The location of the kinase on the projection is consistent with a role in regulating the function of the projection, though other roles for the enzyme are also possible.

摘要

在先前的研究中,我们已经证明微管相关蛋白2(MAP 2)分子由两个结构部分组成。该分子的一部分,称为组装促进结构域,与微管表面结合并负责促进微管组装;另一部分是在微管表面观察到的丝状突起,可能参与微管与其他细胞结构的相互作用。已知MAP 2会因微管制剂中存在的蛋白激酶活性而发生特异性磷酸化。我们现在发现,该活性与MAP 2自身的突起部分共同纯化。当微管蛋白在生物凝胶A - 15m上进行凝胶过滤层析或在DEAE - 葡聚糖凝胶上进行离子交换层析时,激酶活性与MAP 2共洗脱。通过用胰凝乳蛋白酶温和消化,该活性与蛋白酶从微管表面去除MAP 2突起同时从微管中释放出来。通过在生物凝胶A - 15m上对突起进行凝胶过滤层析直接证明了该活性与突起的关联。三种蛋白质种类(相对分子质量分别为39,000、55,000和70,000)与MAP 2共分级分离,其中两种(相对分子质量为39,000和55,000)可能代表相关的环磷酸腺苷依赖性蛋白激酶的亚基。与突起相关的活性被环磷酸腺苷刺激了10倍,并被来自兔骨骼肌的环磷酸腺苷依赖性蛋白激酶抑制剂抑制了95%以上。它似乎代表了与微管相关的唯一显著活性,在微管蛋白、其他微管相关蛋白或MAP 2的组装促进结构域中几乎没有发现活性,并且估计占全脑胞质蛋白激酶活性的7 - 22%。激酶在突起上的定位与调节突起功能的作用一致,不过该酶也可能有其他作用。

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