| Literature DB >> 29605907 |
Brian L Gilmore1, A Cameron Varano1,2, William Dearnaley1, Yanping Liang1, Bridget C Marcinkowski1, Madeline J Dukes3, Deborah F Kelly4,5.
Abstract
Recent advances in technology have enabled single-particle electron microscopy (EM) to rapidly progress as a preferred tool to study protein assemblies. Newly developed materials and methods present viable alternatives to traditional EM specimen preparation. Improved lipid monolayer purification reagents offer considerable flexibility, while ultrathin silicon nitride films provide superior imaging properties to the structural study of protein complexes. Here, we describe the steps for combining monolayer purification with silicon nitride microchips to create a tunable approach for the EM community.Entities:
Keywords: Affinity capture; Electron microscopy; Microchips; Protein assemblies; Silicon nitride; Single-particle analysis
Mesh:
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Year: 2018 PMID: 29605907 PMCID: PMC5947846 DOI: 10.1007/978-1-4939-7759-8_3
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745