Arselin de Châteaubodeau G, Guérin M
Biochimie. 1982 Oct;64(10):883-90. doi: 10.1016/s0300-9084(82)80350-7.
A proteolipid able to bind phosphate has been isolated from yeast mitochondria. During the purification the active protein was always associated with cardiolipin. The cardiolipin requirement for the phosphate binding activity of this proteolipid has been studied using controlled lipid depletion with two phospholipases A2 and with phospholipase C. Only phospholipase A2 from pig pancreas, that deacylated cardiolipin, promoted inhibition of the proteolipid activity (but never more than 70 per cent). Phospholipase A2 from snake venom did not inhibit the binding activity of the proteolipid. Using thin layer chromatography with two sequential solvents it was possible to separate two cardiolipin subspecies; one of them was preferentially hydrolysed by phospholipase C of Bacillus cereus, leading to inhibition of the proteolipid activity. Ca2+ complexed to cardiolipin stoichiometrically (1-1) inhibited the proteolipid activity. This effect could be due to a conformational change in the cardiolipin-protein association.
一种能够结合磷酸盐的蛋白脂质已从酵母线粒体中分离出来。在纯化过程中,活性蛋白始终与心磷脂结合。使用两种磷脂酶A2和磷脂酶C进行可控脂质消耗,研究了这种蛋白脂质的磷酸盐结合活性对心磷脂的需求。只有来自猪胰腺的磷脂酶A2,它使心磷脂脱酰基,促进了蛋白脂质活性的抑制(但从未超过70%)。来自蛇毒的磷脂酶A2没有抑制蛋白脂质的结合活性。使用两种连续溶剂的薄层色谱法可以分离出两种心磷脂亚类;其中一种优先被蜡状芽孢杆菌的磷脂酶C水解,导致蛋白脂质活性受到抑制。与心磷脂化学计量比(1-1)络合的Ca2+抑制了蛋白脂质活性。这种效应可能是由于心磷脂-蛋白质结合中的构象变化。