生物
跨膜蛋白
信号肽酶
生物化学
羊毛甾醇
跨膜结构域
劈理(地质)
脱甲基酶
信号肽
膜拓扑
细胞生物学
肽序列
膜
受体
基因
断裂(地质)
古生物学
胆固醇
甾醇
表观遗传学
作者
Nikita Sergejevs,Dönem Avci,Michael L. van de Weijer,Robin A. Corey,Marius K. Lemberg,Pedro Carvalho
摘要
Cleavage of transmembrane segments on target proteins by the aspartyl intramembrane protease signal peptide peptidase (SPP, encoded by HM13) has been linked to immunity, viral infection and protein quality control. How SPP recognizes its various substrates and specifies their fate remains elusive. Here, we identify the lanosterol demethylase CYP51A1 as an SPP substrate and show that SPP-catalysed cleavage triggers CYP51A1 clearance by endoplasmic reticulum-associated degradation (ERAD). We observe that SPP targets only a fraction of CYP51A1 molecules, and we identify an amphipathic helix in the CYP51A1 N terminus as a key determinant for SPP recognition. SPP recognition is remarkably specific to CYP51A1 molecules with the amphipathic helix aberrantly inserted in the membrane with a type II orientation. Thus, our data are consistent with a role for SPP in topology surveillance, triggering the clearance of certain potentially non-functional conformers.
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