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一种25千道尔顿的嗜热四膜虫EF手型钙离子结合蛋白TCBP-25在细胞皮层中的免疫荧光定位及其在接合过程中的可能作用。

Immunofluorescence localization of a 25-kDa Tetrahymena EF-hand Ca(2+)-binding protein, TCBP-25, in the cell cortex and possible involvement in conjugation.

作者信息

Hanyu K, Takemasa T, Numata O, Takahashi M, Watanabe Y

机构信息

Institute of Biological Sciences, University of Tsukuba, Ibaraki, Japan.

出版信息

Exp Cell Res. 1995 Aug;219(2):487-93. doi: 10.1006/excr.1995.1256.

Abstract

The Tetrahymena Ca(2+)-binding protein of 25 kDa (TCBP-25) is a member of the calmodulin family containing four EF-hand Ca(2+)-binding loops, but its biological role has not yet been investigated. In this study, TCBP-25 was expressed in Escherichia coli as a glutathione S-transferase fusion protein and then purified. Purified TCBP-25 showed a typical Ca(2+)-dependent shift in electrophoretic mobility, consistent with conformational change caused by Ca(2+)-binding. Localization of TCBP-25 was examined by indirect immunofluorescence using an antiserum specific for TCBP-25. Strong immunofluorescence was observed all over the cell cortex except in and around basal bodies. From the results of immunofluorescence using detergent-extracted cells, TCBP-25 is suggested to exist as an insoluble form in the cell cortex. TCBP-25 appears to be localized in the cortical alveoli or the epiplasm and exists around both the migratory and the stationary gametic pronuclei at the pronuclear exchange stage during conjugation. Therefore, we speculate that TCBP-25 may play crucial roles in Ca(2+)-mediated signaling processes in the cell cortex and in a Ca(2+)-dependent pronuclear exchange process during conjugation.

摘要

嗜热四膜虫25 kDa的钙离子结合蛋白(TCBP - 25)是钙调蛋白家族的成员,含有四个EF手型钙离子结合环,但其生物学作用尚未得到研究。在本研究中,TCBP - 25在大肠杆菌中作为谷胱甘肽S - 转移酶融合蛋白表达,然后进行纯化。纯化后的TCBP - 25在电泳迁移率上显示出典型的钙离子依赖性变化,这与钙离子结合引起的构象变化一致。使用针对TCBP - 25的抗血清通过间接免疫荧光法检测TCBP - 25的定位。除了基体及其周围区域外,在整个细胞皮层均观察到强烈的免疫荧光。从使用去污剂提取细胞后的免疫荧光结果来看,TCBP - 25在细胞皮层中似乎以不溶性形式存在。TCBP - 25似乎定位于皮层泡或表质中,并且在接合过程中的原核交换阶段存在于迁移型和静止型配子原核周围。因此,我们推测TCBP - 25可能在细胞皮层中钙离子介导的信号传导过程以及接合过程中钙离子依赖性原核交换过程中发挥关键作用。

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