Difference between revisions of "2010Zhang OpNS"

Revision as of 14:26, 30 June 2020

Citation

Rames, Matthew, Yu, Yadong, and Ren, Gang. Optimized Negative Staining: a High-throughput Protocol for Examining Small and Asymmetric Protein Structure by Electron Microscopy. United States: N. p., 2014. Web. doi:10.3791/51087

Zhang L, Song J, Newhouse Y, Zhang S, Weisgraber KH, Ren G. An optimized negative-staining protocol of electron microscopy for apoE4 POPC lipoprotein. J Lipid Res. 2010;51(5):1228-1236. doi:10.1194/jlr.D002493

Abstract

Apolipoprotein E (apoE), one of the major protein components of lipoproteins in the peripheral and central nervous systems, regulates cholesterol metabolism through its interaction with members of the low density lipoprotein receptor family. One key to understanding apoE function is determining the structure of lipid-bound forms of apoE. Negative-staining (NS) electron microscopy (EM) is an easy and rapid approach for studying the structure and morphology of lipid-bound forms of apoE. However, an artifact of using the conventional NS protocol is that the apoE phospholipid particles form rouleaux. In this study, we used cryo-electron microscopy (cryo-EM) to examine apoE4 palmitoyl-oleoylphosphatidylcholine (POPC) particles in a frozen-hydrated native state. By comparing the particle sizes and shapes produced by different NS protocols to those produced by cryo-EM, we propose an optimized protocol to examine apoE4 POPC particles. Statistical analysis demonstrated that the particle sizes differ by less than 5% between the optimized protocol and the cryo-EM method, with similar shapes. The high contrast and fine detail of particle images produced using this optimized protocol lend themselves to the structural study of lipid-bound forms of apoE.

Keywords

protein structure, lipoprotein structure, electron microscopy, negative-staining, optimized negative-staining protocol, individual-particle electron tomography

Links

https://pubmed.ncbi.nlm.nih.gov/19965615/ https://www.ncbi.nlm.nih.gov/pubmed/29129068 http://www.ncbi.nlm.nih.gov/pubmed/20978167 http://www.nature.com/articles/ncomms11083

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Related methods

https://pubmed.ncbi.nlm.nih.gov/20978167/ https://pubmed.ncbi.nlm.nih.gov/25145703/ https://pubmed.ncbi.nlm.nih.gov/20978167/ https://www.springer.com/gp/book/9781627032742 https://pubmed.ncbi.nlm.nih.gov/23032862/

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