Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
Department of Cell Biology, Yale School of Medicine, New Haven, United States.
Elife. 2020 May 26;9:e57822. doi: 10.7554/eLife.57822.
We have previously shown TANGO1 organises membranes at the interface of the endoplasmic reticulum (ER) and ERGIC/Golgi (Raote et al., 2018). TANGO1 corrals retrograde membranes at ER exit sites to create an export conduit. Here the retrograde membrane is, in itself, an anterograde carrier. This mode of forward transport necessitates a mechanism to prevent membrane mixing between ER and the retrograde membrane. TANGO1 has an unusual membrane helix organisation, composed of one membrane-spanning helix (TM) and another that penetrates the inner leaflet (IM). We have reconstituted these membrane helices in model membranes and shown that TM and IM together reduce the flow of lipids at a region of defined shape. We have also shown that the helices align TANGO1 around an ER exit site. We suggest this is a mechanism to prevent membrane mixing during TANGO1-mediated transfer of bulky secretory cargos from the ER to the ERGIC/Golgi via a tunnel.
我们之前已经表明 TANGO1 在 ER 和 ERGIC/Golgi 的交界处组织膜(Raote 等人,2018 年)。TANGO1 将逆行膜聚集在 ER 出口部位以创建出口导管。在这里,逆行膜本身就是一种顺行载体。这种正向运输方式需要一种机制来防止 ER 和逆行膜之间的膜混合。TANGO1 具有一种不寻常的膜螺旋组织,由一个跨膜螺旋(TM)和另一个穿透内膜的螺旋(IM)组成。我们已经在模型膜中重新构建了这些膜螺旋,并表明 TM 和 IM 共同减少了在特定形状区域的脂质流动。我们还表明,螺旋将 TANGO1 围绕 ER 出口部位排列。我们认为这是一种在 TANGO1 介导的从 ER 向 ERGIC/Golgi 转移大体积分泌货物的过程中防止膜混合的机制,通过隧道进行。