Crites Travis J, Maddox Michael, Padhan Kartika, Muller James, Eigsti Calvin, Varma Rajat
Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
These authors contributed equally to this work.
Curr Protoc Cell Biol. 2015 Sep 1;68:24.5.1-24.5.31. doi: 10.1002/0471143030.cb2405s68.
Glass-supported lipid bilayers presenting freely diffusing proteins have served as a powerful tool for studying cell-cell interfaces, in particular, T cell-antigen presenting cell (APC) interactions, using optical microscopy. Here we expand upon existing protocols and describe the preparation of liposomes by an extrusion method, and describe how this system can be used to study immune synapse formation by Jurkat cells. We also present a method for forming such lipid bilayers on silica beads for the study of signaling responses by population methods, such as western blotting, flow cytometry, and gene-expression analysis. Finally, we describe how to design and prepare transmembrane-anchored protein-laden liposomes, following expression in suspension CHO (CHOs) cells, a mammalian expression system alternative to insect and bacterial cell lines, which do not produce mammalian glycosylation patterns. Such transmembrane-anchored proteins may have many novel applications in cell biology and immunology.
呈现自由扩散蛋白质的玻璃支撑脂质双层,已成为利用光学显微镜研究细胞 - 细胞界面,特别是T细胞 - 抗原呈递细胞(APC)相互作用的有力工具。在此,我们扩展现有方案,描述通过挤压法制备脂质体,并描述该系统如何用于研究Jurkat细胞的免疫突触形成。我们还提出了一种在二氧化硅珠上形成此类脂质双层的方法,用于通过群体方法(如蛋白质印迹、流式细胞术和基因表达分析)研究信号转导反应。最后,我们描述了在悬浮CHO(CHOs)细胞(一种替代昆虫和细菌细胞系的哺乳动物表达系统,其不会产生哺乳动物糖基化模式)中表达后,如何设计和制备负载跨膜锚定蛋白的脂质体。此类跨膜锚定蛋白可能在细胞生物学和免疫学中有许多新应用。