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小角 X 射线和中子散射实验中的复杂性不断增加:从生物膜模拟到活细胞。

Increasing complexity in small-angle X-ray and neutron scattering experiments: from biological membrane mimics to live cells.

机构信息

University of Graz, Institute of Molecular Biosciences, Biophysics Division, NAWI Graz, 8010 Graz, Austria.

出版信息

Soft Matter. 2021 Jan 22;17(2):222-232. doi: 10.1039/c9sm02352f.

Abstract

Small-angle X-ray and neutron scattering are well-established, non-invasive experimental techniques to interrogate global structural properties of biological membrane mimicking systems under physiologically relevant conditions. Recent developments, both in bottom-up sample preparation techniques for increasingly complex model systems, and in data analysis techniques have opened the path toward addressing long standing issues of biological membrane remodelling processes. These efforts also include emerging quantitative scattering studies on live cells, thus enabling a bridging of molecular to cellular length scales. Here, we review recent progress in devising compositional models for joint small-angle X-ray and neutron scattering studies on diverse membrane mimics - with a specific focus on membrane structural coupling to amphiphatic peptides and integral proteins - and live Escherichia coli. In particular, we outline the present state-of-the-art in small-angle scattering methods applied to complex membrane systems, highlighting how increasing system complexity must be followed by an advance in compositional modelling and data-analysis tools.

摘要

小角 X 射线和中子散射是成熟的、非侵入性的实验技术,可以在生理相关条件下研究生物膜模拟系统的整体结构特性。最近的发展,无论是在用于越来越复杂模型系统的自下而上的样品制备技术方面,还是在数据分析技术方面,都为解决生物膜重塑过程中的长期问题开辟了道路。这些努力还包括对活细胞进行新兴的定量散射研究,从而能够实现从分子到细胞尺度的连接。在这里,我们回顾了最近在设计用于不同膜模拟物的小角度 X 射线和中子散射联合研究的组成模型方面的进展-特别关注膜结构与两亲肽和整合蛋白的耦合-以及活大肠杆菌。特别是,我们概述了应用于复杂膜系统的小角散射方法的现状,强调了随着系统复杂性的增加,必须跟进组成建模和数据分析工具的进步。

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