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无序蛋白和蛋白区域对膜曲率感知和重塑的深入了解。

Insights into Membrane Curvature Sensing and Membrane Remodeling by Intrinsically Disordered Proteins and Protein Regions.

机构信息

Physical and Chemical Biology Laboratory and Department of Mechanical Engineering, Indian Institute of Technology Palakkad, Palakkad, Kerala, 678623, India.

Physical and Chemical Biology Laboratory and Department of Physics, Indian Institute of Technology Palakkad, Palakkad, Kerala, 678623, India.

出版信息

J Membr Biol. 2022 Jun;255(2-3):237-259. doi: 10.1007/s00232-022-00237-x. Epub 2022 Apr 22.

Abstract

Cellular membranes are highly dynamic in shape. They can rapidly and precisely regulate their shape to perform various cellular functions. The protein's ability to sense membrane curvature is essential in various biological events such as cell signaling and membrane trafficking. As they are bound, these curvature-sensing proteins may also change the local membrane shape by one or more curvature driving mechanisms. Established curvature-sensing/driving mechanisms rely on proteins with specific structural features such as amphipathic helices and intrinsically curved shapes. However, the recent discovery and characterization of many proteins have shattered the protein structure-function paradigm, believing that the protein functions require a unique structural feature. Typically, such structure-independent functions are carried either entirely by intrinsically disordered proteins or hybrid proteins containing disordered regions and structured domains. It is becoming more apparent that disordered proteins and regions can be potent sensors/inducers of membrane curvatures. In this article, we outline the basic features of disordered proteins and regions, the motifs in such proteins that encode the function, membrane remodeling by disordered proteins and regions, and assays that may be employed to investigate curvature sensing and generation by ordered/disordered proteins.

摘要

细胞膜在形状上具有高度的动态性。它们可以迅速而精确地调节形状,以执行各种细胞功能。蛋白质感知膜曲率的能力对于各种生物事件至关重要,如细胞信号转导和膜运输。当它们被结合时,这些曲率感应蛋白也可以通过一种或多种曲率驱动机制改变局部膜形状。已建立的曲率感应/驱动机制依赖于具有特定结构特征的蛋白质,例如两亲性螺旋和固有弯曲形状。然而,最近许多蛋白质的发现和特征描述打破了蛋白质结构-功能的范例,认为蛋白质功能需要独特的结构特征。通常,这种不依赖于结构的功能完全由无序蛋白质或含有无序区域和结构域的混合蛋白质承担。越来越明显的是,无序蛋白质和区域可以成为膜曲率的有效传感器/诱导剂。在本文中,我们概述了无序蛋白质和区域的基本特征、此类蛋白质中编码功能的基序、无序蛋白质和区域对膜重塑的作用,以及可能用于研究有序/无序蛋白质曲率感应和产生的测定方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2ae/9028910/3dbceefc1bab/232_2022_237_Fig1_HTML.jpg

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