Sumegi B, Freeman D A, Inman L, Srere P A
Pre-clinical Science Unit, VA Medical Center, Dallas, TX 75216.
J Mol Recognit. 1988 Feb;1(1):19-24. doi: 10.1002/jmr.300010105.
We have investigated a possible molecular basis for mitochondrial cristae formation. Proteoliposomes containing electron transport proteins, cytochrome oxidase, or complex III in their proper orientation bind to pig heart mitoplasts but not pig heart mitochondria. Using Leydig tumor cells, we have confirmed earlier reports that chloramphenicol causes a diminution in cristae content and a change in its characteristic lamellar form. We show that the proteoliposomes containing cytochrome oxidase or complex III in the proper orientation bind to mitoplasts from Leydig tumor cells but do not bind as well to mitoplasts from chloramphenicol-treated Leydig tumor cells. These experiments provide a possible mechanism to explain cristae formation.
我们研究了线粒体嵴形成的一种可能的分子基础。含有以正确方向排列的电子传递蛋白、细胞色素氧化酶或复合体III的蛋白脂质体可与猪心脏线粒体膜结合,但不与猪心脏线粒体结合。利用莱迪希肿瘤细胞,我们证实了早期的报道,即氯霉素会导致嵴含量减少及其特征性的层状形态发生改变。我们发现,含有以正确方向排列的细胞色素氧化酶或复合体III的蛋白脂质体可与莱迪希肿瘤细胞的线粒体膜结合,但与经氯霉素处理的莱迪希肿瘤细胞的线粒体膜结合效果不佳。这些实验提供了一种可能的机制来解释嵴的形成。