Rey Martial, Brazzolotto Xavier, Clémençon Benjamin, Afchain Agathe, Brandolin Gérard, Pelosi Ludovic
Laboratoire de Biochimie et Biophysique des Systèmes Intégrés, Institut de Recherches en Technologies et Sciences du Vivant, UMR 5092 CNRS-CEA-Université Joseph Fourier (UJF), CEA-Grenoble, 17 Avenue des Martyrs, 38054 Grenoble Cedex 9, France.
Biochimie. 2007 Sep;89(9):1070-9. doi: 10.1016/j.biochi.2007.03.019. Epub 2007 Apr 10.
Genetic expression versus plasmidic overexpression of a functional recombinant fusion protein combining the yeast Saccharomyces cerevisiae mitochondrial ADP/ATP carrier (Anc2p) and the iso-1-cytochrome c (Cyc1p) has been investigated, with the main aim of increasing the polar surface of the carrier to improve its crystallization properties. The gene encoding the his6-tagged fusion protein was expressed in yeast under the control of the regulatory sequences of ScANC2 or under the control of the strong yeast PMA1 promoter. In both cases, the chimeric carrier, Anc2-Cyc1(His6)p, was able to restore growth on a non-fermentable carbon source of a yeast strain devoid of functional ADP/ATP carrier, demonstrating its transport activity. Nevertheless, when the expression vector was used, the level of expression of Anc2-Cyc1(His6)p was no greater than that of the chimeric carrier obtained in yeast mitochondria after homologous recombination. Optimal conditions to extract and to purify Anc2-Cyc1(His6)p were determined. A series of detergents was screened for their ability to extract and to preserve in vitro the chimeric carrier. A rapid, single step purification of Anc2-Cyc1(His6)p was developed, using n-dodecyl-beta-d-maltoside (DoDM) as the best detergent to solubilize the chimeric protein. Carboxyatractyloside- (CATR-) and nucleotide-binding sites were preserved in the purified protein. Moreover, the Cyc1p moiety of Anc2-Cyc1(His6)p-CATR complex solubilized in DoDM was still able to interact in vitro with the cytochrome c oxidase (COX), with the same affinity as yeast Cyc1p. Improved production and purification of Anc2-Cyc1(His6)p-CATR complex opens up new possibilities for the use of this protein in crystallographic approaches to the yeast ADP/ATP carrier. Furthermore, Anc2-Cyc1(His6)p may be an useful molecular tool to investigate in vivo interactions between components of the respiratory chain complexes such as COX and the proteins implicated in ATP biogenesis, such as the ATP/ADP carrier.
对一种功能性重组融合蛋白进行了基因表达与质粒过表达的研究,该融合蛋白由酿酒酵母线粒体ADP/ATP载体(Anc2p)和异-1-细胞色素c(Cyc1p)组成,主要目的是增加载体的极性表面以改善其结晶特性。编码带有his6标签的融合蛋白的基因在酵母中,在ScANC2调控序列的控制下或在强酵母PMA1启动子的控制下表达。在这两种情况下,嵌合载体Anc2-Cyc1(His6)p都能够恢复缺乏功能性ADP/ATP载体的酵母菌株在非发酵碳源上的生长,证明了其运输活性。然而,当使用表达载体时,Anc2-Cyc1(His6)p的表达水平不高于同源重组后在酵母线粒体中获得的嵌合载体的表达水平。确定了提取和纯化Anc2-Cyc1(His6)p的最佳条件。筛选了一系列去污剂,考察它们提取和体外保存嵌合载体的能力。开发了一种快速、单步纯化Anc2-Cyc1(His6)p的方法,使用正十二烷基-β-D-麦芽糖苷(DoDM)作为溶解嵌合蛋白的最佳去污剂。纯化后的蛋白中保留了羧基苍术苷(CATR)结合位点和核苷酸结合位点。此外,溶解在DoDM中的Anc2-Cyc1(His6)p-CATR复合物的Cyc1p部分仍然能够在体外与细胞色素c氧化酶(COX)相互作用,亲和力与酵母Cyc1p相同。Anc2-Cyc1(His6)p-CATR复合物生产和纯化的改进为该蛋白在酵母ADP/ATP载体晶体学研究中的应用开辟了新的可能性。此外,Anc2-Cyc1(His6)p可能是一种有用的分子工具,用于研究呼吸链复合物成分如COX与参与ATP生物合成的蛋白质如ATP/ADP载体之间的体内相互作用。