Cole Christian M, Brea Roberto J, Kim Young Hun, Hardy Michael D, Yang Jerry, Devaraj Neal K
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Building: Urey Hall 4120, La Jolla, CA 92093 (USA) http://devarajgroup.ucsd.edu.
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Building: Pacific Hall 6160, La Jolla, CA 92093 (USA).
Angew Chem Int Ed Engl. 2015 Oct 19;54(43):12738-42. doi: 10.1002/anie.201504339. Epub 2015 Aug 28.
Transmembrane proteins are critical for signaling, transport, and metabolism, yet their reconstitution in synthetic membranes is often challenging. Non-enzymatic and chemoselective methods to generate phospholipid membranes in situ would be powerful tools for the incorporation of membrane proteins. Herein, the spontaneous reconstitution of functional integral membrane proteins during the de novo synthesis of biomimetic phospholipid bilayers is described. The approach takes advantage of bioorthogonal coupling reactions to generate proteoliposomes from micelle-solubilized proteins. This method was successfully used to reconstitute three different transmembrane proteins into synthetic membranes. This is the first example of the use of non-enzymatic chemical synthesis of phospholipids to prepare proteoliposomes.
跨膜蛋白对信号传导、运输和代谢至关重要,然而它们在合成膜中的重构往往具有挑战性。原位生成磷脂膜的非酶促和化学选择性方法将是整合膜蛋白的强大工具。在此,描述了在仿生磷脂双层从头合成过程中功能性整合膜蛋白的自发重构。该方法利用生物正交偶联反应从胶束增溶的蛋白质生成蛋白脂质体。该方法已成功用于将三种不同的跨膜蛋白重构到合成膜中。这是使用非酶促化学合成磷脂制备蛋白脂质体的首个实例。