Prohibitin and prohibitone are contained in high-molecular weight complexes and interact with alpha-actinin and annexin A2.
The closely related proteins prohibitin (p32) and prohibitone (p37) are evolutionarily conserved with homologues found from cyanobacteria to man. They are thought to be exclusively mitochondrial and have been assigned many-rather different-functions, ranging from a role in lifespan, in mitochondrial inheritance and as chaperones of mitochondrial proteases in yeast. Evidence ... for a localisation outside of mitochondria has been brought forward in mammalian cells, where they influence cell-cycle progression and are found in association with cell surface receptors. We have employed a yeast two-hybrid screen to identify other interacting proteins and have identified alpha-actinin and annexin A2 as binding partners for prohibitin and prohibitone. Coprecipitation experiments supported the putative binding between prohibitin and prohibitone on the one hand and annexin A2 or alpha-actinin on the other hand in intact cells. Surface plasmon resonance analysis was used to determine relative affinities between prohibitin and alpha-actinin and between prohibitone and annexin A2 and alpha-actinin, respectively. We further show that prohibitin and prohibitone can also form homomeric (preferentially tetrameric) and heteromultimeric complexes, with significant affinities.
Mesh Terms:
Actinin, Amino Acid Sequence, Animals, Annexin A2, Binding Sites, Blotting, Western, Chromatography, Gel, DNA-Binding Proteins, Dimerization, Dose-Response Relationship, Drug, Kinetics, Macromolecular Substances, Molecular Sequence Data, Molecular Weight, Precipitin Tests, Protein Binding, Proteins, Receptors, Cell Surface, Repressor Proteins, Sequence Analysis, Sequence Homology, Amino Acid, Surface Plasmon Resonance, Time Factors, Tumor Cells, Cultured, Two-Hybrid System Techniques
Actinin, Amino Acid Sequence, Animals, Annexin A2, Binding Sites, Blotting, Western, Chromatography, Gel, DNA-Binding Proteins, Dimerization, Dose-Response Relationship, Drug, Kinetics, Macromolecular Substances, Molecular Sequence Data, Molecular Weight, Precipitin Tests, Protein Binding, Proteins, Receptors, Cell Surface, Repressor Proteins, Sequence Analysis, Sequence Homology, Amino Acid, Surface Plasmon Resonance, Time Factors, Tumor Cells, Cultured, Two-Hybrid System Techniques
Biochimie
Date: Dec. 01, 2002
PubMed ID: 12628297
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