Narayanareddy K
Institute for physical Biochemistry, University of Munich, Germany.
Biochem Int. 1991 Nov;25(4):733-43.
The ADP/ATP carrier (AAC) from yeast mitochondria has been reconstituted in phospholipid vesicles essentially according to the procedure described for the reconstitution of AAC from bovine heart mitochondria (Krämer and Heberger (1986) Biochim. Biophys. Acta, 863, 289-296). Liposomes were prepared from the mixed micelles of dodecyl octaoxyethylene ether (C12E8)-solubilized protein and egg yolk phosphatidylcholine by removing the detergent with Amberlite treatment. The micelles were treated with Amberlite either by repeatedly passing through small columns filled with Amberlite XAD-2 beads or by stepwise addition of Amberlite beads to the micelles. All the important variables of the reconstitution components were kept at optimal level and the liposomes obtained by both the methods of Amberlite treatment were analysed for (3H)CAT binding, orientation of AAC and nucleotide exchange activity. Reconstituted AAC showed 80% right side out orientation in the liposomes prepared by either procedure. Lipsomes prepared by the Amberlite column procedure exhibited higher CAT binding but lower ADP exchange activity. Liposome preparation by the stepwise addition of Amberlite is suggested to be the method of choice for functional reconstitution of yeast AAC in view of the higher nucleotide transport activity associated with the liposomes prepared by this method.
酵母线粒体的ADP/ATP载体(AAC)已基本按照从牛心线粒体重构AAC的方法(Krämer和Heberger(1986年),《生物化学与生物物理学报》,863卷,289 - 296页)重构于磷脂囊泡中。通过用Amberlite处理去除去污剂,由十二烷基八氧乙烯醚(C12E8)增溶的蛋白质和蛋黄磷脂酰胆碱的混合胶束制备脂质体。胶束用Amberlite处理的方法,要么是反复通过填充有Amberlite XAD - 2珠子的小柱,要么是向胶束中逐步添加Amberlite珠子。重构组分的所有重要变量都保持在最佳水平,并对通过两种Amberlite处理方法获得的脂质体进行(3H)CAT结合、AAC的取向和核苷酸交换活性分析。通过任何一种方法制备的脂质体中,重构的AAC都显示出80%的外向取向。通过Amberlite柱法制备的脂质体表现出更高的CAT结合,但较低的ADP交换活性。鉴于通过该方法制备的脂质体具有更高的核苷酸转运活性,建议通过逐步添加Amberlite的方法制备脂质体,作为酵母AAC功能重构的首选方法。