Department of Physics, Arizona State University, P.O. Box 871504, Tempe, AZ 85287, USA.
Chemical Engineering, School for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, AZ 85287, USA.
Curr Opin Struct Biol. 2019 Oct;58:286-293. doi: 10.1016/j.sbi.2019.06.004. Epub 2019 Jul 22.
In recent years, nano and microcrystals have emerged as a valuable source of high-resolution structural information owing to the invention of serial femtosecond crystallography (SFX) with X-ray free electron lasers and microcrystal electron diffraction (MicroED) using electron cryomicroscopes. Once considered useless for structure determination, nano/microcrystals now confer significant advantages for static and time-resolved structure determination from a wide variety of difficult-to-study targets. MicroED has been used to obtain sub-Ångstrom resolution maps in which hydrogen atoms can be clearly resolved from only a few nano/microcrystals, while SFX has been used to probe protein dynamics following reaction initiation on time scales from femtoseconds to minutes. We review these two complementary techniques and their abilities for high-resolution structure determination.
近年来,随着利用自由电子激光的连续光谱 X 射线结晶学(SFX)和利用电子冷冻显微镜的微晶体电子衍射(MicroED)的发明,纳米和微晶体已经成为高分辨率结构信息的宝贵来源。曾经被认为对结构测定无用的纳米/微晶体,现在为从各种难以研究的目标进行静态和时间分辨结构测定提供了显著的优势。MicroED 已被用于获得亚埃分辨率的图谱,其中仅从少数纳米/微晶体中就可以清楚地分辨出氢原子,而 SFX 则被用于在皮秒到分钟的时间尺度上探测反应起始后的蛋白质动力学。我们回顾了这两种互补技术及其进行高分辨率结构测定的能力。