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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1984-1990 |
| Number of pages | 7 |
| Journal | Structure |
| Volume | 24 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 1 2016 |
All Science Journal Classification (ASJC) codes
- Structural Biology
- Molecular Biology