蛋白质电子显微术

本文简要介绍了蛋白质电子显微术的基本原理和方法,包括低温电镜术和三维重构方法,以及该技术在研究膜蛋白二维晶体、二十面体对称性病毒和非对称性单颗粒蛋白质分子或复合物结构上的应用。随着分辨率的不断提高,蛋白质电子显微术已成为蛋白质结构测定的一种手段。

Towards quantitative determination of atomic structures of amorphous materials in three dimensions

Amorphous materials such as glass,polymer and amorphous alloy have broad applications ranging from daily life to extreme conditions due to their unique properties in elasticity,strength and electrical resistivity.A better understanding of atomic structure of amorphous materials will provide invaluable information for their further engineering and applications.However,experimentally determining the three-dimensional(3D)atomic structure of amorphous materials has been a long-standing problem.Due to the disordered atomic arrangement,amorphous materials do not have any translational and rotational symmetry at long-range scale.Conventional characterization methods,such as the scattering and the microscopy imaging,can only provide the statistic structural information which is averaged over the macroscopic region.The knowledge of the 3D atomic structure of amorphous materials is limited.Recently atomic resolution electron tomography(AET)has proven an increasingly powerful tool for atomic scale structural characterization without any crystalline assumptions,which opens a door to determine the 3D structure of various amorphous materials.In this review,we summarize the state-of-art characterization methods for the exploration of atomic structures of amorphous materials in the past few decades,including X-ray/neutron diffraction,nano-beam and angstrom-beam electron diffraction,fluctuation electron microscopy,high-resolution scanning/transmission electron microscopy,and atom probe tomography.From experimental data and theoretical descriptions,3D structures of various amorphous materials have been built up.Particularly,we introduce the principles and recent progress of AET,and highlight the most recent groundbreaking feat accomplished by AET,i.e.,the first experimental determination of all 3D atomic positions in a multi-component glass-forming alloy and the 3D atomic packing in amorphous solids.We also discuss the new opportunities and challenges for characterizing the chemical and structural defects in amorphous materials.

Cryo-EM for nanomaterials:Progress and perspective

Cryogenic electron microscopy(cryo-EM)has extensively boosted structural biology research since the“resolution revolution”in the year of 2013 which was soon awarded the Nobel Prize in Chemistry in 2017.The advances in camera techniques and software algorithms enabled cryoEM to routinely characterize the three-dimensional structures of biomolecules at near-atomic resolution.Biomolecules are basically sensitive to electron irradiation damage,which can be minimized at cryo-temperature.This principle has inspired material scientists to characterize electron beam-or air-sensitive materials by cryo-EM,such as the electrodes in the lithium-ion battery,metal-organic frameworks(MOFs),covalent-organic frameworks(COFs)and zeolites.In addition,the reaction systems can be fast-frozen at vitreous ice in cryoEM,which correspondingly preserves the materials at the close-to-native state.Herein,we summarized the development and applications of both the cryo-EM technique and other emerging cryo-techniques in materials science,and energy storage and conversion.Cryo-EM techniques,capable of the direct observation of sensitive materials and electrochemical reaction processes,will greatly renew our understanding of materials science and related mechanisms.