| Literature DB >> 32735770 |
Lan Zhu1, Guanhong Bu2, Liang Jing1, Dan Shi3, Ming-Yue Lee1, Tamir Gonen4, Wei Liu5, Brent L Nannenga6.
Abstract
The lipidic cubic phase (LCP) technique has proved to facilitate the growth of high-quality crystals that are otherwise difficult to grow by other methods. However, the crystal size optimization process could be time and resource consuming, if it ever happens. Therefore, improved techniques for structure determination using these small crystals is an important strategy in diffraction technology development. Microcrystal electron diffraction (MicroED) is a technique that uses a cryo-transmission electron microscopy to collect electron diffraction data and determine high-resolution structures from very thin micro- and nanocrystals. In this work, we have used modified LCP and MicroED protocols to analyze crystals embedded in LCP converted by 2-methyl-2,4-pentanediol or lipase, including Proteinase K crystals grown in solution, cholesterol crystals, and human adenosine A2A receptor crystals grown in LCP. These results set the stage for the use of MicroED to analyze microcrystalline samples grown in LCP, especially for those highly challenging membrane protein targets.Entities:
Keywords: GPCR; Proteinase K; additive phase conversion; cholesterol; cryo-electron microscopy (cryo-EM); lipase hydrolysis; lipidic cubic phase (LCP); membrane protein; microcrystal electron diffraction (MicroED); microcrystallography
Year: 2020 PMID: 32735770 PMCID: PMC7544639 DOI: 10.1016/j.str.2020.07.006
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006