PMID:15591068
| Citation |
Sharma, S, Hoskins, JR and Wickner, S (2005) Binding and degradation of heterodimeric substrates by ClpAP and ClpXP. J. Biol. Chem. 280:5449-55 |
|---|---|
| Abstract |
ClpA and ClpX function both as molecular chaperones and as the regulatory components of ClpAP and ClpXP proteases, respectively. ClpA and ClpX bind substrate proteins through specific recognition signals, catalyze ATP-dependent protein unfolding of the substrate, and when in complexes with ClpP translocate the unfolded polypeptide into the cavity of the ClpP peptidase for degradation. To examine the mechanism of interaction of ClpAP with dimeric substrates, single round binding and degradation experiments were performed, revealing that ClpAP degraded both subunits of a RepA homodimer in one cycle of binding. Furthermore, ClpAP was able to degrade both protomers of a RepA heterodimer in which only one subunit contained the ClpA recognition signal. In contrast, ClpXP degraded both subunits of a dimeric substrate only when both protomers contained a recognition signal. These data suggest that ClpAP and ClpXP may recognize and bind substrates in significantly different ways. |
| Links |
PubMed Online version:10.1074/jbc.M412411200 |
| Keywords |
Adenosine Triphosphatases/metabolism; DNA Helicases/genetics; DNA Helicases/metabolism; DNA-Binding Proteins/genetics; DNA-Binding Proteins/metabolism; Dimerization; Endopeptidase Clp/metabolism; Escherichia coli/genetics; Escherichia coli/metabolism; Escherichia coli Proteins/metabolism; Molecular Chaperones/metabolism; Mutation/genetics; Protein Processing, Post-Translational; Protein Subunits/metabolism; RNA/genetics; RNA/metabolism; Substrate Specificity; Trans-Activators/genetics; Trans-Activators/metabolism |
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