Laboratoire de Physique de l'Ecole Normale Supérieure, ENS, Université PSL, CNRS, Sorbonne Université, Université de Paris, 75005 Paris, France; Institute of Psychiatry and Neuroscience of Paris, INSERM U1266, 75014 Paris, France.
Department of Cell Biology, Yale School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA; Nanobiology Institute, Yale University West Campus, West Haven, CT 06516, USA.
Cell Rep. 2023 Jan 31;42(1):111921. doi: 10.1016/j.celrep.2022.111921. Epub 2022 Dec 28.
Tail-anchored (TA) proteins contain a single C-terminal transmembrane domain (TMD) that is captured by the cytosolic Get3 in yeast (TRC40 in humans). Get3 delivers TA proteins to the Get1/2 complex for insertion into the endoplasmic reticulum (ER) membrane. How Get1/2 mediates insertion of TMDs of TA proteins into the membrane is poorly understood. Using bulk fluorescence and microfluidics assays, we show that Get1/2 forms an aqueous channel in reconstituted bilayers. We estimate the channel diameter to be ∼2.5 nm wide, corresponding to the circumference of two Get1/2 complexes. We find that the Get3 binding can seal the Get1/2 channel, which dynamically opens and closes. Our mutation analysis further shows that the Get1/2 channel activity is required to release TA proteins from Get3 for insertion into the membrane. Hence, we propose that the Get1/2 channel functions as an insertase for insertion of TMDs and as a translocase for translocation of C-terminal hydrophilic segments.
尾部锚定(TA)蛋白含有一个单一的 C 端跨膜结构域(TMD),该结构域被酵母中的胞质 Get3(人类中的 TRC40)捕获。Get3 将 TA 蛋白递送至 Get1/2 复合物,以便插入内质网(ER)膜。Get1/2 如何介导 TA 蛋白的 TMD 插入膜中,目前了解甚少。使用批量荧光和微流控测定,我们表明 Get1/2 在重组双层中形成水相通道。我们估计通道直径约为 2.5nm 宽,对应于两个 Get1/2 复合物的周长。我们发现 Get3 结合可以封闭 Get1/2 通道,该通道动态打开和关闭。我们的突变分析进一步表明,Get1/2 通道的活性对于将 TA 蛋白从 Get3 释放以插入膜中是必需的。因此,我们提出 Get1/2 通道作为插入酶,用于插入 TMD,作为转位酶,用于转位 C 端亲水性片段。