6WXB
Cryo-EM Structure of Influenza Hemagglutinin (HA) Trimer Vitrified Using Back-it-up
6WXB の概要
| エントリーDOI | 10.2210/pdb6wxb/pdb |
| EMDBエントリー | 21954 |
| 分子名称 | Hemagglutinin, 2-acetamido-2-deoxy-beta-D-glucopyranose, beta-D-mannopyranose (3 entities in total) |
| 機能のキーワード | hemagglutinin, trimer, influenza, back-it-up, through-grid wicking, viral protein |
| 由来する生物種 | Influenza A virus (strain A/Hong Kong/1/1968 H3N2) |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 191760.61 |
| 構造登録者 | |
| 主引用文献 | Tan, Y.Z.,Rubinstein, J.L. Through-grid wicking enables high-speed cryoEM specimen preparation. Acta Crystallogr D Struct Biol, 76:1092-1103, 2020 Cited by PubMed Abstract: Blotting times for conventional cryoEM specimen preparation complicate time-resolved studies and lead to some specimens adopting preferred orientations or denaturing at the air-water interface. Here, it is shown that solution sprayed onto one side of a holey cryoEM grid can be wicked through the grid by a glass-fiber filter held against the opposite side, often called the `back', of the grid, producing a film suitable for vitrification. This process can be completed in tens of milliseconds. Ultrasonic specimen application and through-grid wicking were combined in a high-speed specimen-preparation device that was named `Back-it-up' or BIU. The high liquid-absorption capacity of the glass fiber compared with self-wicking grids makes the method relatively insensitive to the amount of sample applied. Consequently, through-grid wicking produces large areas of ice that are suitable for cryoEM for both soluble and detergent-solubilized protein complexes. The speed of the device increases the number of views for a specimen that suffers from preferred orientations. PubMed: 33135680DOI: 10.1107/S2059798320012474 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.9 Å) |
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