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PMID: 8011660 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Fo membrane domain of ATP synthase from bovine heart mitochondria: purification, subunit composition, and reconstitution with F1-ATPase.

Biochemistry ·Vol. 33 ·No. 25 ·1994-06-28 ·Pages 7971-8

Collinson IR, Runswick MJ, Buchanan SK, Fearnley IM, Skehel JM, van Raaij MJ, Griffiths DE, Walker JE

Abstract

The Fo membrane domain of the F1Fo-ATP synthase complex has been purified from bovine heart mitochondria. The purification procedure involves the removal of peripheral membrane proteins, including F1-ATPase, from submitochondrial particles with guanidine hydrochloride, followed by extraction of Fo and other membrane proteins from the stripped membranes in the presence of the detergent n-dodecyl beta-D-maltoside. Fo was then purified by ion-exchange and dye ligand chromatography in the presence of the same detergent. Approximately 15 mg of pure Fo was recovered from 1.8 g of mitochondrial membrane protein. The purified Fo is a complex of nine different polypeptides. They are subunits a, b, c, d, e, F6, and A6L characterized before in F1Fo-ATPase preparations, and two new hitherto undetected subunits, named f and g. The sequences of subunits f and g have been determined. They are not related significantly to any known protein, but subunit f appears to contain a membrane-spanning alpha-helix. Proteins f and g are also present in approximately stoichiometric amounts in a highly purified preparation of intact F1Fo-ATPase, and so it is concluded that they are authentic subunits of the bovine enzyme with unknown functions. Dibutyltin 3-hydroxyflavone, an inhibitor of F1Fo-ATPase, also binds to the purified Fo in detergent and competes for binding with venturicidin. In the presence of F1 and OSCP, the purified Fo was reassembled into the intact F1Fo-ATPase complex. Therefore, this procedure provides a relatively abundant source of pure and functional Fo that is suitable for structural analysis.

MeSH Terms
Adenosine Triphosphatases/metabolism Amino Acid Sequence Animals Carrier Proteins Cattle Intracellular Membranes/enzymology Macromolecular Substances Mass Spectrometry Membrane Proteins/chemistry,metabolism Mitochondria, Heart/enzymology Mitochondrial Proton-Translocating ATPases Molecular Sequence Data Proton-Translocating ATPases/chemistry Submitochondrial Particles/enzymology
Chemicals
Carrier Proteins Macromolecular Substances Membrane Proteins Adenosine Triphosphatases Mitochondrial Proton-Translocating ATPases Proton-Translocating ATPases oligomycin sensitivity-conferring protein
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Collinson I R
MRC Laboratory of Molecular Biology, Cambridge, U.K.
Runswick M J
Buchanan S K
Fearnley I M
Skehel J M
van Raaij M J
Griffiths D E
Walker J E
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1994-06-28
Pages
7971-8
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Databases
GENBANK
S70447, S70448
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