Engel A, Hoenger A, Hefti A, Henn C, Ford R C, Kistler J, Zulauf M
M.E. Müller-Institute for High-Resolution Electron Microscopy at the Biocenter, Univeristy of Basel, Switzerland.
J Struct Biol. 1992 Nov-Dec;109(3):219-34. doi: 10.1016/1047-8477(92)90035-9.
Membrane protein reconstitution into two-dimensional (2-D) ordered arrays is described. The assembly of 2-D crystals may be modeled as a two-step process: the membrane protein is first integrated in the lipid bilayer and then crystallized by removal of excess detergent or lipid and/or by precipitating agents. Lipid-detergent, protein-detergent, and lipid-protein interactions are critical during the first step, while lipid-protein and protein-protein interactions dominate events in the second step. The evidence supporting this model results from quasielastic light scattering analyses and electron microscopy of different lipid-detergent systems and reconstitution experiments with Escherichia coli porin OmpF, Phormidium laminosum photosystem I reaction centers, and integral membrane proteins of mammalian lens fiber cells.
描述了膜蛋白重构为二维(2-D)有序阵列的过程。二维晶体的组装可被模拟为一个两步过程:膜蛋白首先整合到脂质双层中,然后通过去除过量的去污剂或脂质和/或通过沉淀剂使其结晶。脂质-去污剂、蛋白质-去污剂以及脂质-蛋白质相互作用在第一步中至关重要,而脂质-蛋白质和蛋白质-蛋白质相互作用在第二步中主导整个过程。支持该模型的证据来自不同脂质-去污剂系统的准弹性光散射分析和电子显微镜观察,以及对大肠杆菌孔蛋白OmpF、层状席藻光合系统I反应中心和哺乳动物晶状体纤维细胞整合膜蛋白的重构实验。