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网格蛋白包被在胞吞作用期间部分预组装并随后弯曲。

Clathrin coats partially preassemble and subsequently bend during endocytosis.

机构信息

Cell Biology and Biophysics, European Molecular Biology Laboratory , Heidelberg, Germany.

Department of Biochemistry, University of Geneva , Geneva, Switzerland.

出版信息

J Cell Biol. 2023 Mar 6;222(3). doi: 10.1083/jcb.202206038. Epub 2023 Feb 3.

Abstract

Eukaryotic cells use clathrin-mediated endocytosis to take up a large range of extracellular cargo. During endocytosis, a clathrin coat forms on the plasma membrane, but it remains controversial when and how it is remodeled into a spherical vesicle. Here, we use 3D superresolution microscopy to determine the precise geometry of the clathrin coat at large numbers of endocytic sites. Through pseudo-temporal sorting, we determine the average trajectory of clathrin remodeling during endocytosis. We find that clathrin coats assemble first on flat membranes to 50% of the coat area before they become rapidly and continuously bent, and this mechanism is confirmed in three cell lines. We introduce the cooperative curvature model, which is based on positive feedback for curvature generation. It accurately describes the measured shapes and dynamics of the clathrin coat and could represent a general mechanism for clathrin coat remodeling on the plasma membrane.

摘要

真核细胞利用网格蛋白介导的胞吞作用来摄取大量的细胞外物质。在胞吞作用过程中,网格蛋白衣被在质膜上形成,但它何时以及如何重塑为球形囊泡仍然存在争议。在这里,我们使用 3D 超分辨率显微镜来确定大量胞吞部位的网格蛋白衣被的精确几何形状。通过伪时间排序,我们确定了胞吞过程中网格蛋白重塑的平均轨迹。我们发现,网格蛋白衣被首先在平面膜上组装,达到衣被面积的 50%,然后迅速且连续地弯曲,这一机制在三种细胞系中得到了证实。我们引入了协同曲率模型,该模型基于曲率生成的正反馈。它准确地描述了测量到的网格蛋白衣被的形状和动力学,并可能代表质膜上网格蛋白衣被重塑的一般机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19c/9929656/d0801e05464b/JCB_202206038_Fig1.jpg

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