| Literature DB >> 27806259 |
Guimei Yu1, Kunpeng Li1, Pengwei Huang2, Xi Jiang2, Wen Jiang3.
Abstract
The affinity cryoelectron microscopy (cryo-EM) approach has been explored in recent years to simplify and/or improve the sample preparation for cryo-EM, which can bring previously challenging specimens such as those of low abundance and/or unpurified ones within reach of the cryo-EM technique. Despite the demonstrated successes for solving structures to low to intermediate resolutions, the lack of near-atomic structures using this approach has led to a common perception of affinity cryo-EM as a niche technique incapable of reaching high resolutions. Here, we report a ∼2.6-Å structure solved using the antibody-based affinity grid approach with low-concentration Tulane virus purified from a low-yield cell-culture system that has been challenging to standard cryo-EM grid preparation. Quantitative analyses of the structure indicate data and reconstruction quality comparable with the conventional grid preparation method using samples at high concentration.Entities:
Keywords: Tulane virus; affinity cryoelectron microscopy; antibody-based affinity grid; single-particle 3D reconstruction
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Year: 2016 PMID: 27806259 PMCID: PMC5123806 DOI: 10.1016/j.str.2016.09.008
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006