PMID:9468613
| Citation |
Wilkens, S, Rodgers, A, Ogilvie, I and Capaldi, RA (1997) Structure and arrangement of the delta subunit in the E. coli ATP synthase (ECF1F0). Biophys. Chem. 68:95-102 |
|---|---|
| Abstract |
F1F0 type ATPases are made up of two parts, an F1, which contains three catalytic sites on beta subunits, and an F0 which contains the proton channel. These two domains have been visualized in electron microscopy as linked by a narrow stalk of around 45 A in length. Biochemical studies have provided clear evidence that the gamma and epsilon subunits are components of this stalk. There is an emerging consensus that the gamma and epsilon subunits rotate relative to the alpha 3 beta 3 domain as part of the cooperativity and energy coupling within the complex. Two other subunits are required to link the F1 to F0 in the E. coli enzyme, and these are the delta and b subunits. The structure of a major part of the delta subunit (residues 1-134) has now been obtained by NMR spectroscopy. The main feature is a six alpha-helix bundle, which provides the N-terminal domain of the delta subunit. This domain interacts with the F1 core via the N-terminal part of the alpha subunit. The C-terminal domain of delta is less well defined. This part is required for binding to the F0 part by direct interaction with the b subunits. It is argued that delta and the two copies of the b subunit are components of a second stalk linking the F1 and F0 parts, which acts as a stator to allow the energy-linked rotational movements of delta and epsilon subunits. |
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| Keywords |
Amino Acid Sequence; Binding Sites; Escherichia coli/enzymology; Macromolecular Substances; Molecular Sequence Data; Nuclear Magnetic Resonance, Biomolecular/methods; Protein Conformation; Proton-Translocating ATPases/chemistry; Proton-Translocating ATPases/metabolism; Proton-Translocating ATPases/physiology |
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