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微绒毛110K-钙调蛋白:核苷酸对分离的细胞骨架的影响以及纯化复合物与F-肌动蛋白的相互作用。

Microvillus 110K-calmodulin: effects of nucleotides on isolated cytoskeletons and the interaction of the purified complex with F-actin.

作者信息

Verner K, Bretscher A

出版信息

J Cell Biol. 1985 May;100(5):1455-65. doi: 10.1083/jcb.100.5.1455.

Abstract

Microvilli isolated from intestinal epithelial cells contain a cytoskeletal Mr 110,000 polypeptide complexed with calmodulin (110K-CM) that is believed to link the microfilament core bundle laterally to the plasma membrane. Previous work has shown that physiological levels of ATP can partially solubilize the 110K-CM complex from isolated microvillus cytoskeletons or isolated microvilli. However, once extracted, the 110K-CM complex has been found to be difficult to maintain stably soluble in aqueous buffers. This is due to the presence of an endogenous ATPase (approximately 100 nmol Pi/min per mg at 37 degrees C) in microvillus cytoskeletal preparations that depletes the ATP with subsequent precipitation of 110K-CM. Addition of ATP to such precipitates resolubilizes 110K-CM. Inclusion of an ATP regenerating system in the solubilization of 110K-CM from cytoskeletons, or membrane-bound brush borders, increases the amount of 110K-CM solubilized. Solubilization of 110K-CM from microvillus cytoskeletons was found to require a divalent cation (Mg2+, Mn2+, or Co2+, but not Zn2+) and a nucleoside triphosphate (ATP, GTP, CTP, or ITP). ADP did not solubilize 110K-CM, but could partially inhibit ATP-dependent solubilization. Solubilized 110K was phosphorylated during extraction of microvillus cores with [gamma-32P]ATP, but this was unrelated to the solubilization of 110K-CM as the endogenous kinase was specific for ATP, whereas the solubilization was not. The 110K-CM was purified using ATP extraction of brush border cytoskeletons in the presence of an ATP regenerating system, gel filtration of the solubilized extract, an ATP depletion step to specifically precipitate 110K-CM with F-actin, and resolubilization followed by phosphocellulose chromatography. The purified complex was stably soluble in aqueous buffers both in the presence and absence of ATP. It bound almost quantitatively to F-actin in the absence of ATP, and showed nucleotide solubilization characteristics from F-actin similar to that found for solubilization of 110K-CM from microvillus cores. At low ATP levels, the binding to F-actin was increased in the presence of ADP. These results suggest that the purified complex has been isolated in a native form. The data confirm and extend the studies of Howe and Mooseker (1983, J. Cell Biol., 97:974-985) using a partially purified preparation of 110K-CM and further emphasize that 110K-CM is a stably water soluble complex and not an integral membrane protein.

摘要

从肠上皮细胞分离出的微绒毛含有一种细胞骨架110,000道尔顿的多肽,它与钙调蛋白复合(110K-CM),据信这种复合物将微丝核心束横向连接到质膜上。先前的研究表明,生理水平的ATP能使110K-CM复合物从分离的微绒毛细胞骨架或分离的微绒毛中部分溶解。然而,一旦提取出来,发现110K-CM复合物很难在水性缓冲液中稳定地保持溶解状态。这是由于微绒毛细胞骨架制剂中存在一种内源性ATP酶(37℃时每毫克约100 nmol无机磷/分钟),它会消耗ATP,随后导致110K-CM沉淀。向这种沉淀物中添加ATP可使110K-CM重新溶解。在从细胞骨架或膜结合的刷状缘溶解110K-CM时加入ATP再生系统,可增加溶解的110K-CM的量。发现从微绒毛细胞骨架中溶解110K-CM需要二价阳离子(Mg2+、Mn2+或Co2+,但不是Zn2+)和核苷三磷酸(ATP、GTP、CTP或ITP)。ADP不能溶解110K-CM,但可部分抑制ATP依赖性溶解。在用[γ-32P]ATP提取微绒毛核心的过程中,溶解的110K被磷酸化,但这与110K-CM的溶解无关,因为内源性激酶对ATP具有特异性,而溶解过程并非如此。在ATP再生系统存在的情况下,通过ATP提取刷状缘细胞骨架、对溶解提取物进行凝胶过滤、用ATP耗尽步骤使110K-CM与F-肌动蛋白特异性沉淀,然后重新溶解并进行磷酸纤维素层析,从而纯化110K-CM。纯化后的复合物在有无ATP的情况下都能稳定地溶解于水性缓冲液中。在没有ATP的情况下,它几乎能定量地与F-肌动蛋白结合,并且从F-肌动蛋白上的核苷酸溶解特性类似于从微绒毛核心中溶解110K-CM的情况。在低ATP水平下,在ADP存在时与F-肌动蛋白的结合增加。这些结果表明,纯化后的复合物是以天然形式分离得到的。这些数据证实并扩展了豪和穆斯克(1983年,《细胞生物学杂志》,97:974-985)使用部分纯化的110K-CM制剂进行的研究,并进一步强调110K-CM是一种稳定的水溶性复合物,而不是一种整合膜蛋白。

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