Brandolin G, Le Saux A, Trezeguet V, Vignais P V, Lauquin G J
UA 1130 du CNRS, Département de Biologie Moléculaire et Structurale, Grenoble, France.
Biochem Biophys Res Commun. 1993 Apr 15;192(1):143-50. doi: 10.1006/bbrc.1993.1393.
The yeast mitochondrial adenine nucleotide carrier isoform encoded by the ANC2 gene has been specifically expressed in a yeast strain disrupted for the two other genes, ANC1 and ANC3. Isolation of the carrier in a functional form was achieved by utilisation of a mixture of two detergents, dodecylmaltoside and Emulphogen. The intrinsic fluorescence of the Anc2 protein was specifically and rapidly enhanced upon addition of the transportable nucleotides ADP and ATP. Fluorescence enhancement was prevented or reversed by the addition of a stoichiometric amount of CATR. Addition of CATR alone elicited a dose-dependent decrease of fluorescence. The ANC2-specific yeast stain offers the means to study a single ADP/ATP carrier, with a well-defined amino acid sequence, suitable for analysis of substrate- or inhibitor-induced conformational changes.
由ANC2基因编码的酵母线粒体腺嘌呤核苷酸载体同工型已在破坏了另外两个基因ANC1和ANC3的酵母菌株中特异性表达。通过使用两种去污剂(十二烷基麦芽糖苷和乳化剂)的混合物实现了功能性载体的分离。添加可转运核苷酸ADP和ATP后,Anc2蛋白的固有荧光特异性且迅速增强。添加化学计量的CATR可阻止或逆转荧光增强。单独添加CATR会引起荧光的剂量依赖性降低。ANC2特异性酵母菌株提供了研究单个ADP/ATP载体的方法,该载体具有明确的氨基酸序列,适用于分析底物或抑制剂诱导的构象变化。