8DFC
CryoEM structure of the 1:1 ADP-tetrafluoroaluminate stabilized nitrogenase complex from Azotobacter vinelandii
8DFC の概要
エントリーDOI | 10.2210/pdb8dfc/pdb |
EMDBエントリー | 27404 27405 |
分子名称 | Nitrogenase molybdenum-iron protein alpha chain, TETRAFLUOROALUMINATE ION, MAGNESIUM ION, ... (12 entities in total) |
機能のキーワード | nitrogenase, metalloenzyme, metal binding protein, oxidoreductase |
由来する生物種 | Azotobacter vinelandii 詳細 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 297796.25 |
構造登録者 | |
主引用文献 | Warmack, R.A.,Wenke, B.B.,Spatzal, T.,Rees, D.C. Anaerobic cryoEM protocols for air-sensitive nitrogenase proteins. Nat Protoc, 2024 Cited by PubMed Abstract: Single-particle cryo-electron microscopy (cryoEM) provides an attractive avenue for advancing our atomic resolution understanding of materials, molecules and living systems. However, the vast majority of published cryoEM methodologies focus on the characterization of aerobically purified samples. Air-sensitive enzymes and microorganisms represent important yet understudied systems in structural biology. We have recently demonstrated the success of an anaerobic single-particle cryoEM workflow applied to the air-sensitive nitrogenase enzymes. In this protocol, we detail the use of Schlenk lines and anaerobic chambers to prepare samples, including a protein tag for monitoring sample exposure to oxygen in air. We describe how to use a plunge freezing apparatus inside of a soft-sided vinyl chamber of the type we routinely use for anaerobic biochemistry and crystallography of oxygen-sensitive proteins. Manual control of the airlock allows for introduction of liquid cryogens into the tent. A custom vacuum port provides slow, continuous evacuation of the tent atmosphere to avoid accumulation of flammable vapors within the enclosed chamber. These methods allowed us to obtain high-resolution structures of both nitrogenase proteins using single-particle cryoEM. The procedures involved can be generally subdivided into a 4 d anaerobic sample generation procedure, and a 1 d anaerobic cryoEM sample preparation step, followed by conventional cryoEM imaging and processing steps. As nitrogen is a substrate for nitrogenase, the Schlenk lines and anaerobic chambers described in this procedure are operated under an argon atmosphere; however, the system and these procedures are compatible with other controlled gas environments. PubMed: 38575747DOI: 10.1038/s41596-024-00973-5 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (2.48 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード
