Biochemistry Department, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755; email:
Institute of Biochemistry, ETH Zurich, Zurich CH-8093, Switzerland.
Annu Rev Cell Dev Biol. 2016 Oct 6;32:197-222. doi: 10.1146/annurev-cellbio-111315-125016. Epub 2016 Jun 8.
Transport of newly synthesized proteins from the endoplasmic reticulum (ER) to the Golgi complex is highly selective. As a general rule, such transport is limited to soluble and membrane-associated secretory proteins that have reached properly folded and assembled conformations. To secure the efficiency, fidelity, and control of this crucial transport step, cells use a combination of mechanisms. The mechanisms are based on selective retention of proteins in the ER to prevent uptake into transport vesicles, on selective capture of proteins in COPII carrier vesicles, on inclusion of proteins in these vesicles by default as part of fluid and membrane bulk flow, and on selective retrieval of proteins from post-ER compartments by retrograde vesicle transport.
新合成的蛋白质从内质网(ER)向高尔基体复合物的转运是高度选择性的。一般来说,这种转运仅限于已达到正确折叠和组装构象的可溶性和膜相关分泌蛋白。为了确保这个关键转运步骤的效率、保真度和控制,细胞使用了一系列机制。这些机制基于在 ER 中选择性地保留蛋白质以防止其被摄取到转运小泡中,选择性地捕获 COPII 载体小泡中的蛋白质,默认情况下将蛋白质包含在这些小泡中,作为流体和膜的一部分,以及通过逆行囊泡运输从 ER 后区室中选择性地回收蛋白质。