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网格蛋白介导的胞吞作用的系统生物学和物理生物学。

Systems biology and physical biology of clathrin-mediated endocytosis.

机构信息

Department of Bioengineering, University of Pennsylvania, 210 South 33rd Street, Philadelphia, PA 19104, USA.

出版信息

Integr Biol (Camb). 2011 Aug;3(8):803-15. doi: 10.1039/c1ib00036e. Epub 2011 Jul 26.

Abstract

In this review, we describe the application of experimental data and modeling of intracellular endocytic trafficking mechanisms with a focus on the process of clathrin-mediated endocytosis. A detailed parts-list for the protein-protein interactions in clathrin-mediated endocytosis has been available for some time. However, recent experimental, theoretical, and computational tools have proved to be critical in establishing a sequence of events, cooperative dynamics, and energetics of the intracellular process. On the experimental front, total internal reflection fluorescence microscopy, photo-activated localization microscopy, and spinning-disk confocal microscopy have focused on assembly and patterning of endocytic proteins at the membrane, while on the theory front, minimal theoretical models for clathrin nucleation, biophysical models for membrane curvature and bending elasticity, as well as methods from computational structural and systems biology, have proved insightful in describing membrane topologies, curvature mechanisms, and energetics.

摘要

在这篇综述中,我们描述了实验数据的应用和细胞内内吞运输机制的建模,重点介绍了网格蛋白介导的内吞作用的过程。一段时间以来,网格蛋白介导的内吞作用中蛋白质-蛋白质相互作用的详细部件清单已经可用。然而,最近的实验、理论和计算工具被证明对于确定细胞内过程的事件顺序、协同动力学和能量学至关重要。在实验方面,全内反射荧光显微镜、光激活定位显微镜和旋转盘共聚焦显微镜集中研究了膜上内吞蛋白的组装和模式,而在理论方面,网格蛋白成核的最小理论模型、膜曲率和弯曲弹性的生物物理模型,以及计算结构和系统生物学的方法,在描述膜拓扑、曲率机制和能量学方面都被证明具有启发性。

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