Gasnier F, Rousson R, Lermé F, Vaganay E, Louisot P, Gateau-Roesch O
Department of Biochemistry, INSERM-CNRS 189, Lyon-Sud Medical School, Oullins, France.
Anal Biochem. 1993 Jul;212(1):173-8. doi: 10.1006/abio.1993.1309.
Human mitochondria were isolated from placenta by a combination of differential and Percoll gradient centrifugation, resulting in a highly pure and intact preparation as assessed by marker enzyme analysis and electron microscopy. The advantages over previous methods are the rapidity of the procedure and the excellent resolution of mitochondria and lysosomes. Moreover, the high extent of intactness of the mitochondria so obtained made them particularly well suited for investigating outer membrane proteins. Taking advantage of this method, we have purified human mitochondrial porin. The purified protein consists of a single unglycosylated polypeptide of molecular mass 33 kDa.
通过差速离心和Percoll梯度离心相结合的方法从胎盘中分离出人类线粒体,经标记酶分析和电子显微镜评估,得到了高度纯净且完整的制剂。该方法相对于以前的方法的优势在于操作快速,以及线粒体和溶酶体的分辨率极佳。此外,如此获得的线粒体完整程度很高,使其特别适合用于研究外膜蛋白。利用这种方法,我们纯化了人类线粒体孔蛋白。纯化后的蛋白质由一条分子量为33 kDa的单一非糖基化多肽组成。