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使用荧光显微镜定量细胞膜突起上的膜几何形状和蛋白质分选。

Quantification of membrane geometry and protein sorting on cell membrane protrusions using fluorescence microscopy.

机构信息

Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ, United States.

Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ, United States.

出版信息

Methods Enzymol. 2024;700:385-411. doi: 10.1016/bs.mie.2024.01.023. Epub 2024 Apr 16.

Abstract

Plasma membranes are flexible and can exhibit numerous shapes below the optical diffraction limit. The shape of cell periphery can either induce or be a product of local protein density changes, encoding numerous cellular functions. However, quantifying membrane curvature and the ensuing sorting of proteins in live cells remains technically demanding. Here, we demonstrate the use of simple widefield fluorescence microscopy to study the geometrical properties (i.e., radius, length, and number) of thin membrane protrusions. Importantly, the quantification of protrusion radius establishes a platform for studying the curvature preferences of membrane proteins.

摘要

质膜具有柔韧性,可以在低于光学衍射极限的情况下呈现出多种形状。细胞边缘的形状可以诱导或成为局部蛋白质密度变化的产物,从而编码众多的细胞功能。然而,在活细胞中定量膜曲率和随之而来的蛋白质分拣仍然具有技术挑战性。在这里,我们展示了使用简单的宽场荧光显微镜来研究薄质膜突起的几何性质(即半径、长度和数量)。重要的是,突起半径的定量为研究膜蛋白的曲率偏好提供了一个平台。

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