Institut für Biochemie der Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany.
Biochem Biophys Res Commun. 2011 Oct 28;414(3):528-32. doi: 10.1016/j.bbrc.2011.09.100. Epub 2011 Sep 24.
In eukaryotes, membrane and soluble proteins of the secretory pathway enter the endoplasmic reticulum (ER) after synthesis in an unfolded state. Directly after entry, most proteins are modified with glycans at suitable glycosylation sites and start to fold. A protein that cannot fold properly will be degraded in a process called ER associated degradation (ERAD). Failures in ERAD, either by loss of function or by premature degradation of proteins, are a cause of severe diseases. Therefore, the search for novel ERAD components to gain better insight in this process is of high importance. Carbohydrate trimming is a relevant process in ER quality control. In this work a novel putative yeast mannosidase encoded by the open reading frame YLR057W was identified and named Mnl2. Deletion of MNL2 diminished the degradation efficiency of misfolded CPY(*) in the absence of the cognate mannosidase Mnl1, indicating a specific role in ERAD.
在真核生物中,膜蛋白和分泌途径中的可溶性蛋白在合成时处于未折叠状态,进入内质网(ER)。进入内质网后,大多数蛋白质在合适的糖基化位点被糖基化修饰并开始折叠。不能正确折叠的蛋白质将在称为内质网相关降解(ERAD)的过程中被降解。ERAD 的失败,无论是由于功能丧失还是蛋白质过早降解,都是严重疾病的原因。因此,寻找新的 ERAD 成分以更好地了解这一过程非常重要。糖基化修剪是 ER 质量控制的一个相关过程。在这项工作中,鉴定并命名了一个由开放阅读框 YLR057W 编码的新型酵母甘露糖苷酶,命名为 Mnl2。在没有同源甘露糖苷酶 Mnl1 的情况下,mnl2 缺失降低了错误折叠的 CPY(*)的降解效率,表明其在 ERAD 中具有特定作用。