Department of Biochemistry and Biotechnology, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki 036-8561, Japan.
Arch Biochem Biophys. 2011 Mar 15;507(2):254-61. doi: 10.1016/j.abb.2010.12.003. Epub 2010 Dec 9.
Although mitochondrial μ- and m-calpains play significant roles in apoptotic cell death, their activating mechanisms have not been determined. The purpose of this study was to determine the core factors that are involved in activating mitochondrial outer membrane (OM)-bound calpains. To accomplish this, we solubilized OM-bound calpains and separated them by DEAE-Sepharose column chromatography, and identified them by immunoblots. We also determined the core factors that activated the OM-bound calpains and release them from the OM by calpain assays, immunoprecipitations, and immunoblots. The OM-bound m-calpain large subunit was not associated with the small subunit or with Grp75 chaperone. Free calpain small subunit was located in the IMS and caused the release of the OM-bound m-calpain large subunit from the OM together with Grp75, ATP, and Ca²+. Our results showed that the activating mechanism of mitochondrial OM-bound m-calpain and the release of mitochondrial m-calpain from the OM have important implications in facilitating apoptotic cell death.
尽管线粒体 μ-和 m-钙蛋白酶在细胞凋亡中发挥重要作用,但它们的激活机制尚未确定。本研究旨在确定参与激活线粒体外膜(OM)结合钙蛋白酶的核心因素。为此,我们通过 DEAE-Sepharose 柱层析溶解 OM 结合钙蛋白酶,并通过免疫印迹鉴定它们。我们还通过钙蛋白酶测定、免疫沉淀和免疫印迹确定了激活 OM 结合钙蛋白酶并将其从 OM 中释放出来的核心因素。OM 结合的 m-钙蛋白酶大亚基不与小亚基或 Grp75 伴侣结合。游离的钙蛋白酶小亚基位于 IMS 中,并导致 OM 结合的 m-钙蛋白酶大亚基与 Grp75、ATP 和 Ca²+一起从 OM 中释放出来。我们的结果表明,线粒体 OM 结合的 m-钙蛋白酶的激活机制以及线粒体 m-钙蛋白酶从 OM 中的释放,对促进细胞凋亡具有重要意义。