McCracken A A, Brodsky J L
University of Nevada, Biology Department, Reno 89557, USA.
J Cell Biol. 1996 Feb;132(3):291-8. doi: 10.1083/jcb.132.3.291.
To investigate the mechanisms of ER-associated protein degradation (ERAD), this process was reconstituted in vitro. Established procedures for post-translational translocation of radiolabeled prepro-alpha factor into isolated yeast microsomes were modified to inhibit glycosylation and to include a posttranslocation "chase" incubation period to monitor degradation. Glycosylation was inhibited with a glyco-acceptor peptide to compete for core carbohydrates, or by using a radio-labeled alpha factor precursor that had been genetically engineered to eliminate all three glycosylation sites. Inhibition of glycosylation led to the production of unglycosylated pro-alpha factor (p alpha F), a processed form of the alpha factor precursor shown to be a substrate of ERAD in vivo. With this system, both glycosylated and unglycosylated forms of pro-alpha factor were stable throughout a 90-min chase incubation. However, the addition of cytosol to the chase incubation reaction induced a selective and rapid degradation of p alpha F. These results directly reflect the behavior of alpha factor precursor in vivo; i.e., p alpha F is a substrate for ERAD, while glycosylated pro-alpha factor is not. Heat inactivation and trypsin treatment of cytosol, as well as addition of ATP gamma S to the chase incubations, led to a stabilization of p alpha F. ERAD was observed in sec12 microsomes, indicating that export of p alpha F via transport vesicles was not required. Furthermore, p alpha F but not glycosylated pro-alpha factor was found in the supernatant of the chase incubation reactions, suggesting a specific transport system for this ERAD substrate. Finally, the degradation of p alpha F was inhibited when microsomes from a yeast strain containing a disrupted calnexin gene were examined. Together, these results indicate that cytosolic protein factor(s), ATP hydrolysis, and calnexin are required for ER-associated protein degradation in yeast, and suggest the cytosol as the site for degradation.
为了研究内质网相关蛋白降解(ERAD)的机制,该过程在体外进行了重建。将放射性标记的前原α因子进行翻译后转运到分离的酵母微粒体中的既定程序进行了修改,以抑制糖基化,并包括一个转运后“追踪”孵育期以监测降解。通过使用糖受体肽竞争核心碳水化合物来抑制糖基化,或者使用经过基因工程改造以消除所有三个糖基化位点的放射性标记的α因子前体。糖基化的抑制导致了未糖基化的前α因子(pαF)的产生,α因子前体的这种加工形式在体内被证明是ERAD的底物。使用该系统,在90分钟的追踪孵育过程中,糖基化和未糖基化形式的前α因子都是稳定的。然而,在追踪孵育反应中加入细胞质会诱导pαF的选择性快速降解。这些结果直接反映了α因子前体在体内的行为;即,pαF是ERAD的底物,而糖基化的前α因子不是。对细胞质进行热灭活和胰蛋白酶处理,以及在追踪孵育中加入ATPγS,导致pαF的稳定。在sec12微粒体中观察到了ERAD,这表明不需要通过转运囊泡输出pαF。此外,在追踪孵育反应的上清液中发现了pαF而不是糖基化的前α因子,这表明存在针对这种ERAD底物的特定转运系统。最后,当检查来自含有破坏的钙连蛋白基因的酵母菌株的微粒体时,pαF的降解受到抑制。总之,这些结果表明,细胞质蛋白因子、ATP水解和钙连蛋白是酵母内质网相关蛋白降解所必需的,并表明细胞质是降解的位点。