Kutay U, Ahnert-Hilger G, Hartmann E, Wiedenmann B, Rapoport T A
Max-Delbrück, Centre for Molecular Medicine, Berlin-Buch.
EMBO J. 1995 Jan 16;14(2):217-23. doi: 10.1002/j.1460-2075.1995.tb06994.x.
Synaptobrevin/vesicle-associated membrane protein is one of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins. It is proposed to provide specificity for the targeting and fusion of vesicles with the plasma membrane. It belongs to a class of membrane proteins which lack a signal sequence and contain a single hydrophobic segment close to their C-terminus, leaving most of the polypeptide chain in the cytoplasm (tail-anchored). We show that in neuroendocrine PC12 cells, synaptobrevin is not directly incorporated into the target organelle, synaptic-like vesicles. Rather, it is first inserted into the endoplasmic reticulum (ER) membrane and is then transported via the Golgi apparatus. Its insertion into the ER membrane in vitro occurs post-translationally, is dependent on ATP and results in a trans-membrane orientation of the hydrophobic tail. Membrane integration requires ER protein(s) different from the translocation components needed for proteins with signal sequences, thus suggesting a novel mechanism of insertion.
突触小泡蛋白/囊泡相关膜蛋白是可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)蛋白之一。有人提出它为囊泡与质膜的靶向和融合提供特异性。它属于一类缺乏信号序列且在其C端附近含有单个疏水片段的膜蛋白,使得大部分多肽链位于细胞质中(尾锚定)。我们发现,在神经内分泌PC12细胞中,突触小泡蛋白并非直接整合到靶细胞器即类突触小泡中。相反,它首先插入内质网(ER)膜,然后通过高尔基体运输。它在体外插入ER膜是在翻译后发生的,依赖于ATP,并导致疏水尾的跨膜取向。膜整合需要不同于具有信号序列的蛋白质所需的易位成分的ER蛋白,因此提示了一种新的插入机制。