Volkmann Niels
Sanford-Burnham Medical Research Institute, La Jolla, California, USA.
Methods Enzymol. 2010;483:31-46. doi: 10.1016/S0076-6879(10)83002-2.
Electron tomography has become a powerful tool for revealing the molecular architecture of biological cells and tissues. In principle, electron tomography can provide high-resolution mapping of entire proteomes. The achievable resolution (3-8 nm) is capable of bridging the gap between live-cell imaging and atomic resolution structures. However, the relevant information is not readily accessible from the data and needs to be identified, extracted, and processed before it can be used. Because electron tomography imaging and image acquisition technologies have enjoyed major advances in the last few years and continue to increase data throughput, the need for approaches that allow automatic and objective interpretation of electron tomograms becomes more and more urgent. This chapter provides an overview of the state of the art in this field and attempts to identify the major bottlenecks that prevent approaches for interpreting electron tomography data to develop their full potential.
电子断层扫描已成为揭示生物细胞和组织分子结构的强大工具。原则上,电子断层扫描可以提供整个蛋白质组的高分辨率图谱。可实现的分辨率(3-8纳米)能够弥合活细胞成像和原子分辨率结构之间的差距。然而,相关信息不易从数据中获取,在使用之前需要进行识别、提取和处理。由于电子断层扫描成像和图像采集技术在过去几年取得了重大进展,并且数据通量持续增加,因此对能够自动、客观解释电子断层扫描图的方法的需求变得越来越迫切。本章概述了该领域的现状,并试图找出阻碍电子断层扫描数据解释方法充分发挥其潜力的主要瓶颈。