Interaction of Amphipols with Sarcoplasmic Reticulum Ca2+-ATPase
| Autor: | Philippe Champeil, Thierry Menguy, Marc le Maire, Christophe Tribet, J.-L. Popot |
|---|---|
| Rok vydání: | 2000 |
| Předmět: |
Protein Denaturation
Aqueous solution biology Polymers Chemistry ATPase Endoplasmic reticulum Detergents Calcium-Transporting ATPases Cell Biology Hydrogen-Ion Concentration Binding Competitive Biochemistry Sarcoplasmic Reticulum Solubility Membrane protein Amphiphile biology.protein Atpase activity Particle Size Binding site Molecular Biology Incubation |
| Zdroj: | Journal of Biological Chemistry. 275:18623-18637 |
| ISSN: | 0021-9258 |
| Popis: | Amphipols are short-chain amphipathic polymers designed to keep membrane proteins soluble in aqueous solutions. We have evaluated the effects of the interaction of amphipols with sarcoplasmic reticulum Ca(2+)-ATPase either in a membrane-bound or a soluble form. If the addition of amphipols to detergent-solubilized ATPase was followed by removal of detergent, soluble complexes formed, but these complexes retained poor ATPase activity, were not very stable upon long incubation periods, and at high concentrations they experienced aggregation. Nevertheless, adding excess detergent to diluted detergent-free ATPase-amphipol complexes incubated for short periods immediately restored full activity to these complexes, showing that amphipols had protected solubilized ATPase from the rapid and irreversible inactivation that otherwise follows detergent removal. Amphipols also protected solubilized ATPase from the rapid and irreversible inactivation observed in detergent solutions if the ATPase Ca(2+) binding sites remain vacant. Moreover, in the presence of Ca(2+), amphipol/detergent mixtures stabilized concentrated ATPase against inactivation and aggregation, whether in the presence or absence of lipids, for much longer periods of time (days) than detergent alone. Our observations suggest that mixtures of amphipols and detergents are promising media for handling solubilized Ca(2+)-ATPase under conditions that would otherwise lead to its irreversible denaturation and/or aggregation. |
| Databáze: | OpenAIRE |
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