Department of Physics, The Ohio State University, Columbus, OH 43210, USA.
Department of Nuclear Engineering, University of New Mexico, Albuquerque, NM 87131, USA.
Dev Cell. 2021 Nov 22;56(22):3146-3159.e5. doi: 10.1016/j.devcel.2021.10.019. Epub 2021 Nov 12.
Sculpting a flat patch of membrane into an endocytic vesicle requires curvature generation on the cell surface, which is the primary function of the endocytosis machinery. Using super-resolved live cell fluorescence imaging, we demonstrate that curvature generation by individual clathrin-coated pits can be detected in real time within cultured cells and tissues of developing organisms. Our analyses demonstrate that the footprint of clathrin coats increases monotonically during the formation of pits at different levels of plasma membrane tension. These findings are only compatible with models that predict curvature generation at the early stages of endocytic clathrin pit formation. We also found that CALM adaptors associated with clathrin plaques form clusters, whereas AP2 distribution is more homogenous. Considering the curvature sensing and driving roles of CALM, we propose that CALM clusters may increase the strain on clathrin lattices locally, eventually giving rise to rupture and subsequent pit completion at the edges of plaques.
将平坦的膜片塑造成内吞小泡需要在细胞表面产生曲率,这是内吞作用机制的主要功能。使用超分辨活细胞荧光成像,我们证明了在培养细胞和发育生物组织中,可以实时检测到单个网格蛋白包被陷窝的曲率生成。我们的分析表明,在不同的质膜张力水平下,网格蛋白包被的足迹在陷窝形成过程中单调增加。这些发现与预测内吞网格蛋白陷窝形成早期曲率生成的模型是一致的。我们还发现,与网格蛋白斑相关的 CALM 衔接蛋白形成簇,而 AP2 的分布则更均匀。考虑到 CALM 在曲率感应和驱动中的作用,我们提出 CALM 簇可能会局部增加网格蛋白晶格的应变,最终导致斑块边缘的破裂和随后的陷窝完成。