7V66
Structure of Apoferritin
7V66 の概要
| エントリーDOI | 10.2210/pdb7v66/pdb |
| EMDBエントリー | 31736 |
| 分子名称 | Ferritin heavy chain (1 entity in total) |
| 機能のキーワード | complex, transport protein, oxidoreductase |
| 由来する生物種 | Homo sapiens (Human) |
| タンパク質・核酸の鎖数 | 24 |
| 化学式量合計 | 482797.13 |
| 構造登録者 | |
| 主引用文献 | Wu, C.,Shi, H.,Zhu, D.,Fan, K.,Zhang, X. Low-cooling-rate freezing in biomolecular cryo-electron microscopy for recovery of initial frames. QRB Discov, 2:-, 2021 Cited by PubMed Abstract: When biological samples are first exposed to electrons in cryo-electron microcopy (cryo-EM), proteins exhibit a rapid 'burst' phase of beam-induced motion that cannot be corrected with software. This lowers the quality of the initial frames, which are the least damaged by the electrons. Hence, they are commonly excluded or down-weighted during data processing, reducing the undamaged signal and the resolution in the reconstruction. By decreasing the cooling rate during sample preparation, either with a cooling-rate gradient or by increasing the freezing temperature, we show that the quality of the initial frames for various protein and virus samples can be recovered. Incorporation of the initial frames in the reconstruction increases the resolution by an amount equivalent to using ~60% more data. Moreover, these frames preserve the high-quality cryo-EM densities of radiation-sensitive residues, which is often damaged or very weak in canonical three-dimensional reconstruction. The improved freezing conditions can be easily achieved using existing devices and enhance the overall quality of cryo-EM structures. PubMed: 37529673DOI: 10.1017/qrd.2021.8 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (1.89 Å) |
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