University of Michigan, Ann Arbor, MI, USA.
Baylor College of Medicine, Houston, TX, USA.
Methods Mol Biol. 2022;2433:105-120. doi: 10.1007/978-1-0716-1998-8_6.
Membrane proteins are essential components in cell membranes and enable cells to communicate with their outside environment and to carry out intracellular signaling. Functional reconstitution of complex membrane proteins using cell-free expression (CFE) systems has been proved to be challenging mainly due to the lack of necessary machinery for proper folding and translocation of nascent membrane proteins and their delivery to the supplied synthetic bilayers. Here, we provide protocols for detergent-free, cell-free reconstitution of functional membrane proteins using HeLa-based CFE system and outline assays for studying their membrane insertion, topology, and their orientation upon incorporation into the supported lipid bilayers or bilayers of giant unilamellar vesicles as well as methods to isolate functional translocated cell-free produced membrane proteins.
膜蛋白是细胞膜的重要组成部分,使细胞能够与外界环境进行通讯,并进行细胞内信号转导。使用无细胞表达(CFE)系统对复杂膜蛋白进行功能重建一直是具有挑战性的,主要是由于缺乏正确折叠和易位新生膜蛋白所需的机制,以及将其递送到提供的合成双层的机制。在这里,我们提供了使用基于 HeLa 的 CFE 系统进行无去污剂、无细胞功能重建的方案,并概述了用于研究它们在插入膜、拓扑结构以及在整合到支持的脂质双层或巨大的单分子层囊泡的双层中的方向的测定方法,以及分离功能转移的无细胞产生的膜蛋白的方法。