Micro-electron diffraction (MicroED) is an emerging technique to use cryo-electron microscope to study the crystal structures of macromolecule from its micro-/nano-crystals, which are not suitable for conventional X-ray crystallography. However, this technique has been prevented for its wide application by the limited availability of producing good micro-/nano-crystals and the inappropriate transfer of crystals. Here, we developed a complete workflow to prepare suitable crystals efficiently for MicroED experiment. This workflow includes in situ on-grid crystallization, single-side blotting, cryo-focus ion beam (cryo-FIB) fabrication, and cryo-electron diffraction of crystal cryo-lamella. This workflow enables us to apply MicroED to study many small macromolecular crystals with the size of 2-10 μm, which is too large for MicroED but quite small for conventional X-ray crystallography. We have applied this method to solve 2.5 à crystal structure of lysozyme from its micro-crystal within the size of 10âÃâ10âÃâ10 μm(3). Our work will greatly expand the availability space of crystals suitable for MicroED and fill up the gap between MicroED and X-ray crystallography.
In situ protein micro-crystal fabrication by cryo-FIB for electron diffraction.
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作者:Li Xinmei, Zhang Shuangbo, Zhang Jianguo, Sun Fei
| 期刊: | Biophysics Reports | 影响因子: | 0.000 |
| 时间: | 2018 | 起止号: | 2018;4(6):339-347 |
| doi: | 10.1007/s41048-018-0075-x | ||
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