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内吞摄取过程中的糖脂和凝集素

Glycolipids and Lectins in Endocytic Uptake Processes.

作者信息

Johannes Ludger, Wunder Christian, Shafaq-Zadah Massiullah

机构信息

Institut Curie, PSL Research University, Chemical Biology of Membranes and Therapeutic Delivery unit, INSERM, U 1143, CNRS, UMR 3666, 26 rue d'Ulm, 75248 Paris Cedex 05, France.

Institut Curie, PSL Research University, Chemical Biology of Membranes and Therapeutic Delivery unit, INSERM, U 1143, CNRS, UMR 3666, 26 rue d'Ulm, 75248 Paris Cedex 05, France.

出版信息

J Mol Biol. 2016 Oct 27. doi: 10.1016/j.jmb.2016.10.027.

Abstract

A host of endocytic processes has been described at the plasma membrane of eukaryotic cells. Their categorization has most commonly referenced cytosolic machinery, of which the clathrin coat has occupied a preponderant position. In what concerns intra-membrane constituents, the focus of interest has been on phosphatidylinositol lipids and their capacity to orchestrate endocytic events on the cytosolic leaflet of the membrane. The contribution of extracellular determinants to the construction of endocytic pits has received much less attention, depite the fact that (glyco)sphingolipids are exoplasmic leaflet fabric of membrane domains, termed rafts, whose contributions to predominantly clathrin-independent internalization processes is well recognized. Furthermore, sugar modifications on extracellular domains of proteins, and sugar-binding proteins, termed lectins, have also been linked to the uptake of endocytic cargoes at the plasma membrane. In this review, we first summarize these contributions by extracellular determinants to the endocytic process. We thus propose a molecular hypothesis - termed the GL-Lect hypothesis - on how GlycoLipids and Lectins drive the formation of compositional nanoenvrionments from which the endocytic uptake of glycosylated cargo proteins is operated via clathrin-independent carriers. Finally, we position this hypothesis within the global context of endocytic pathway proposals that have emerged in recent years.

摘要

在真核细胞的质膜上,已经描述了许多内吞过程。它们的分类最常参考胞质机制,其中网格蛋白包被占据主导地位。在膜内成分方面,人们关注的焦点一直是磷脂酰肌醇脂质及其在膜胞质小叶上协调内吞事件的能力。细胞外决定因素对内吞小窝形成的贡献受到的关注要少得多,尽管(糖)鞘脂是膜结构域(称为脂筏)外质小叶的组成部分,其对主要不依赖网格蛋白的内化过程的贡献已得到充分认识。此外,蛋白质细胞外结构域上的糖修饰以及称为凝集素的糖结合蛋白也与质膜上内吞货物的摄取有关。在这篇综述中,我们首先总结细胞外决定因素对内吞过程的这些贡献。因此,我们提出了一个分子假说——称为GL-Lect假说——关于糖脂和凝集素如何驱动组成性纳米环境的形成,糖基化货物蛋白通过不依赖网格蛋白的载体从该环境中进行内吞摄取。最后,我们将这个假说置于近年来出现的内吞途径假说的整体背景中。

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