Gallet P F, Zachowski A, Julien R, Fellmann P, Devaux P F, Maftah A
Institut de Biotechnologie, Faculté des Sciences, 123 avenue A. Thomas, 87060, Limoges cedex, France.
Biochim Biophys Acta. 1999 Apr 14;1418(1):61-70. doi: 10.1016/s0005-2736(99)00022-x.
The transmembrane diffusion and equilibrium distribution of spin-labelled phosphatidylethanolamine (PE*), phosphatidylcholine (PC*) and cardiolipin (CL*) were investigated in purified mitochondrial inner membranes using electron spin resonance spectroscopy. Using the back exchange technique, we found that the outside-inside movement of PE* and PC* in beef-heart inner mitochondrial membranes was rapid (t1/2 in the range 10-15 min at 30 degrees C). The steady-state distributions in non-energised mitoplasts were approximately 30% in the inner leaflet for PC* and 39% for PE*. Within the limits of probe concentration that can possibly be used in these experiments, the initial velocity of the inward movement was not saturable with respect to the amount of analogue added to the membranes, suggesting that the spin-labelled phospholipids diffused passively between the two leaflets of the inner mitochondrial membrane. In energised mitoplasts, PC* behaviour was not affected, PE* diffused approximately two times faster toward the inner monolayer but reached the same plateau. Treatment of energised mitochondria with N-ethylmaleimide did not affect PC* diffusion, while the kinetics of PE* internalisation became identical to that of PC*. Similar results were found when PC* and PE* movements were studied in mitoplasts from beef heart, rat liver or yeast. The spin-labelled cardiolipin, which possesses four long chains, had to be introduced in the mitoplast with some ethanol. After equilibration (t1/2 of the order of 13 min at 30 degrees C), the transmembrane distribution suggested that approximately half of the cardiolipin analogue remained in the outer leaflet. These results do not allow us to determine if a specific protein (or flippase) is involved in the phospholipid transmembrane traffic within inner mitochondrial membranes, but they show that lipids can rapidly flip through the mitochondrial membrane.
利用电子自旋共振光谱法,研究了自旋标记的磷脂酰乙醇胺(PE*)、磷脂酰胆碱(PC*)和心磷脂(CL*)在纯化的线粒体内膜中的跨膜扩散和平衡分布。采用反向交换技术,我们发现牛肉心线粒体内膜中PE和PC的外向-内向运动很快(30℃时t1/2在10-15分钟范围内)。在无能量的线粒体中,PC在内侧小叶的稳态分布约为30% , PE为39%。在这些实验可能使用的探针浓度范围内,内向运动的初始速度相对于添加到膜上的类似物的量不饱和,这表明自旋标记的磷脂在线粒体内膜的两个小叶之间被动扩散。在有能量的线粒体中, PC的行为不受影响,PE向内单层的扩散速度快约两倍,但达到相同的平台期。用N-乙基马来酰亚胺处理有能量 的线粒体不影响PC的扩散,而PE内化动力学变得与PC相同。当在牛肉心、大鼠肝脏或酵母 的线粒体中研究PC和PE*运动时,也发现了类似结果。具有四条长链的自旋标记的心磷脂必须与一些乙醇一起引入线粒体。平衡后(30℃时t1/2约为13分钟),跨膜分布表明约一半的心磷脂类似物留在外侧小叶。这些结果无法让我们确定是否有特定蛋白质(或翻转酶)参与线粒体内膜内的磷脂跨膜运输,但它们表明脂质可以快速翻转通过线粒体膜。