Kalyana Sundaram Ramalingam Venkat, Bera Manindra, Coleman Jeff, Weerakkody Jonathan S, Krishnakumar Shyam S, Ramakrishnan Sathish
Nanobiology Institute, Yale University School of Medicine, West Haven, CT, 06516, USA.
Department of Cell Biology, Yale University School of Medicine, New Haven, CT, 06520, USA.
Small. 2022 Dec;18(51):e2205567. doi: 10.1002/smll.202205567. Epub 2022 Nov 3.
Cellular plasma membranes, in their role as gatekeepers to the external environment, host numerous protein assemblies and lipid domains that manage the movement of molecules into and out of cells, regulate electric potential, and direct cell signaling. The ability to investigate these roles on the bilayer at a single-molecule level in a controlled, in vitro environment while preserving lipid and protein architectures will provide deeper insights into how the plasma membrane works. A tunable silicon microarray platform that supports stable, planar, and asymmetric suspended lipid membranes (SLIM) using synthetic and native plasma membrane vesicles for single-molecule fluorescence investigations is developed. Essentially, a "plasma membrane-on-a-chip" system that preserves lipid asymmetry and protein orientation is created. By harnessing the combined potential of this platform with total internal reflection fluorescence (TIRF) microscopy, the authors are able to visualize protein complexes with single-molecule precision. This technology has widespread applications in biological processes that happen at the cellular membranes and will further the knowledge of lipid and protein assemblies.
细胞质膜作为细胞与外部环境之间的门户,承载着众多蛋白质组装体和脂质结构域,这些结构域负责管理分子进出细胞的运动、调节电势并指导细胞信号传导。在可控的体外环境中,在单分子水平上研究这些结构域在双层膜上的作用,同时保留脂质和蛋白质结构,将有助于更深入地了解质膜的工作原理。本文开发了一种可调谐硅微阵列平台,该平台使用合成的和天然的质膜囊泡来支持稳定、平面且不对称的悬浮脂质膜(SLIM),用于单分子荧光研究。本质上,构建了一个保留脂质不对称性和蛋白质取向的“芯片上的质膜”系统。通过将该平台与全内反射荧光(TIRF)显微镜的综合潜力相结合,作者能够以单分子精度可视化蛋白质复合物。这项技术在发生于细胞膜的生物过程中具有广泛应用,并将增进对脂质和蛋白质组装体的认识。