Pinson B, Pillois X, Brèthes D, Chevallier J, Napias C
Institut de Biochimie et Génétique Cellulaires du Centre National de la Recherche Scientifique, Bordeaux, France.
Eur J Biochem. 1996 Jul 15;239(2):439-44. doi: 10.1111/j.1432-1033.1996.0439u.x.
The purine/cytosine permease, encoded by the FCY2 gene, is a carrier located in the plasma membrane of the yeast Saccharomyces cerevisiae. Polyclonal antibodies were raised against two peptides that corresponded to the sub-N-terminal and C-terminal sequences of the putative protein deduced from the FCY2 gene. Immunoprecipitation experiments performed with protein extracts labelled in vivo with 35S showed that purine/cytosine permease is specifically detected as a broad and diffuse band. The apparent molecular mass of this protein was 45-50 kDa. By means of in vivo pulse/chase 35S-labelling experiments, we observed a slight increase in the apparent molecular mass of purine/cytosine permease during the chase. This shift in electrophoretic mobility of the protein suggested a post-translational modification. This molecular mass increase was eliminated by alkaline phosphatase treatment of the immunoprecipitate, which strongly suggested phosphorylation of the carrier. This proposal was confirmed by in vivo [32P]P(i) labelling and immunoprecipitation of purine/cytosine permease with purified anti-(sub-N-terminal peptide) IgG or anti-(C-terminal peptide) IgG. Phosphoamino acid analysis indicated that phosphorylation occurred on seryl residues of purine/cytosine permease. By means of thermosensitive secretory-pathway-mutant strains, we demonstrated that purine/cytosine permease phosphorylation occurred either between the Golgi apparatus and the plasma membrane or in the plasma membrane itself.
由FCY2基因编码的嘌呤/胞嘧啶通透酶是一种位于酿酒酵母质膜上的载体。针对两条与从FCY2基因推导的假定蛋白质的亚N端和C端序列相对应的肽段制备了多克隆抗体。用体内经35S标记的蛋白质提取物进行的免疫沉淀实验表明,嘌呤/胞嘧啶通透酶被特异性检测为一条宽且弥散的条带。该蛋白质的表观分子量为45 - 50 kDa。通过体内脉冲/追踪35S标记实验,我们观察到在追踪过程中嘌呤/胞嘧啶通透酶的表观分子量略有增加。该蛋白质电泳迁移率的这种变化表明存在翻译后修饰。通过对免疫沉淀物进行碱性磷酸酶处理消除了这种分子量增加,这强烈提示该载体发生了磷酸化。通过体内[32P]P(i)标记以及用纯化的抗(亚N端肽段)IgG或抗(C端肽段)IgG对嘌呤/胞嘧啶通透酶进行免疫沉淀,证实了这一推测。磷酸氨基酸分析表明磷酸化发生在嘌呤/胞嘧啶通透酶的丝氨酸残基上。通过温度敏感型分泌途径突变株,我们证明嘌呤/胞嘧啶通透酶的磷酸化发生在高尔基体和质膜之间或质膜本身。