Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1179752 | Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics | 2006 | 4 Pages |
Abstract
NADH:quinone oxidoreductases (NDHs), constitute one of the electron entry points into membrane-bound respiratory chains, oxidising NADH and reducing quinones. Type-II NDHs (NDH-2) are functionally unable to translocate protons and are typically constituted by a single â¼50 kDa subunit lacking iron-sulfur clusters and containing one flavin as the sole redox centre. No three dimensional crystal structure is yet available for NDHs. We describe the crystallisation and preliminary structure determination of a NDH-2 that contains a covalently bound FAD, isolated from the membrane fraction of Acidianus ambivalens, a hyperthermoacidophilic archaeon capable of growing at 80 °C and pH 2.0. NDH-2 was solubilised with the detergent n-dodecyl-β-d-maltoside and crystallised using ammonium phosphate as precipitant. The structure was solved by MIRAS using Pt and I derivatives.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
José A. Brito, Tiago M. Bandeiras, Miguel Teixeira, Clemens Vonrhein, Margarida Archer,