Cappuccio Jenny A, Hinz Angela K, Kuhn Edward A, Fletcher Julia E, Arroyo Erin S, Henderson Paul T, Blanchette Craig D, Walsworth Vickie L, Corzett Michele H, Law Richard J, Pesavento Joseph B, Segelke Brent W, Sulchek Todd A, Chromy Brett A, Katzen Federico, Peterson Todd, Bench Graham, Kudlicki Wieslaw, Hoeprich Paul D, Coleman Matthew A
Biosciences and Biotechnology Division, Lawrence Livermore National Laboratory, Livermore, CA, USA.
Methods Mol Biol. 2009;498:273-96. doi: 10.1007/978-1-59745-196-3_18.
Membrane-associated proteins and protein complexes account for approximately a third or more of the proteins in the cell (1, 2). These complexes mediate essential cellular processes; including signal transduc-tion, transport, recognition, bioenergetics and cell-cell communication. In general, membrane proteins are challenging to study because of their insolubility and tendency to aggregate when removed from their protein lipid bilayer environment. This chapter is focused on describing a novel method for producing and solubilizing membrane proteins that can be easily adapted to high-throughput expression screening. This process is based on cell-free transcription and translation technology coupled with nanolipoprotein par ticles (NLPs), which are lipid bilayers confined within a ring of amphipathic protein of defined diameter. The NLPs act as a platform for inserting, solubilizing and characterizing functional membrane proteins. NLP component proteins (apolipoproteins), as well as membrane proteins can be produced by either traditional cell-based or as discussed here, cell-free expression methodologies.
膜相关蛋白和蛋白复合物约占细胞中蛋白质的三分之一或更多(1,2)。这些复合物介导基本的细胞过程,包括信号转导、运输、识别、生物能量学和细胞间通讯。一般来说,膜蛋白因其不溶性以及从蛋白质脂质双分子层环境中移除时易于聚集的特性而难以研究。本章重点描述一种生产和溶解膜蛋白的新方法,该方法可轻松适用于高通量表达筛选。此过程基于无细胞转录和翻译技术,结合纳米脂蛋白颗粒(NLP),纳米脂蛋白颗粒是限定直径的两亲性蛋白环内的脂质双分子层。纳米脂蛋白颗粒作为插入、溶解和表征功能性膜蛋白的平台。纳米脂蛋白颗粒组成蛋白(载脂蛋白)以及膜蛋白可以通过传统的基于细胞的方法或此处讨论的无细胞表达方法来生产。