Literature DB >> 10555973

ClpA and ClpP remain associated during multiple rounds of ATP-dependent protein degradation by ClpAP protease.

S K Singh1, F Guo, M R Maurizi.   

Abstract

The Escherichia coli ClpA and ClpP proteins form a complex, ClpAP, that catalyzes ATP-dependent degradation of proteins. Formation of stable ClpA hexamers and stable ClpAP complexes requires binding of ATP or nonhydrolyzable ATP analogues to ClpA. To understand the order of events during substrate binding, unfolding, and degradation by ClpAP, it is essential to know the oligomeric state of the enzyme during multiple catalytic cycles. Using inactive forms of ClpA or ClpP as traps for dissociated species, we measured the rates of dissociation of ClpA hexamers or ClpAP complexes. When ATP was saturating, the rate constant for dissociation of ClpA hexamers was 0.032 min(-1) (t(1/2) of 22 min) at 37 degrees C, and dissociation of ClpP from the ClpAP complexes occurred with a rate constant of 0. 092 min(-1) (t(1/2) of 7.5 min). Because the k(cat) for casein degradation is approximately 10 min(-1), these results indicate that tens of molecules of casein can be turned over by the ClpAP complex before significant dissociation occurs. Mutations in the N-terminal ATP binding site led to faster rates of ClpA and ClpAP dissociation, whereas mutations in the C-terminal ATP binding site, which cause significant decreases in ATPase activity, led to lower rates of dissociation of ClpA and ClpAP complexes. Dissociation rates for wild-type and first domain mutants of ClpA were faster at low nucleotide concentrations. The t(1/2) for dissociation of ClpAP complexes in the presence of nonhydrolyzable analogues was >/=30 min. Thus, ATP binding stabilizes the oligomeric state of ClpA, and cycles of ATP hydrolysis affect the dynamics of oligomer interaction. However, since the k(cat) for ATP hydrolysis is approximately 140 min(-1), ClpA and the ClpAP complex remain associated during hundreds of rounds of ATP hydrolysis. Our results indicate that the ClpAP complex is the functional form of the protease and as such engages in multiple rounds of interaction with substrate proteins, degradation, and release of peptide products without dissociation.

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Year:  1999        PMID: 10555973     DOI: 10.1021/bi991615f

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  21 in total

1.  Unfolding and internalization of proteins by the ATP-dependent proteases ClpXP and ClpAP.

Authors:  S K Singh; R Grimaud; J R Hoskins; S Wickner; M R Maurizi
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-01       Impact factor: 11.205

2.  Energy-dependent degradation: Linkage between ClpX-catalyzed nucleotide hydrolysis and protein-substrate processing.

Authors:  Randall E Burton; Tania A Baker; Robert T Sauer
Journal:  Protein Sci       Date:  2003-05       Impact factor: 6.725

3.  Alternating translocation of protein substrates from both ends of ClpXP protease.

Authors:  Joaquin Ortega; Hyun Sook Lee; Michael R Maurizi; Alasdair C Steven
Journal:  EMBO J       Date:  2002-09-16       Impact factor: 11.598

4.  Quantitative NMR spectroscopy of supramolecular complexes: dynamic side pores in ClpP are important for product release.

Authors:  Remco Sprangers; Anna Gribun; Peter M Hwang; Walid A Houry; Lewis E Kay
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-01       Impact factor: 11.205

5.  ATP-dependent proteases differ substantially in their ability to unfold globular proteins.

Authors:  Prakash Koodathingal; Neil E Jaffe; Daniel A Kraut; Sumit Prakash; Susan Fishbain; Christophe Herman; Andreas Matouschek
Journal:  J Biol Chem       Date:  2009-04-21       Impact factor: 5.157

6.  Stable isotope labeling with amino acids in cell culture based mass spectrometry approach to detect transient protein interactions using substrate trapping.

Authors:  Stefani N Thomas; Yunhu Wan; Zhongping Liao; Phyllis I Hanson; Austin J Yang
Journal:  Anal Chem       Date:  2011-06-15       Impact factor: 6.986

7.  Catalytic turnover triggers exchange of subunits of the magnesium chelatase AAA+ motor unit.

Authors:  Joakim Lundqvist; Ilka Braumann; Marzena Kurowska; André H Müller; Mats Hansson
Journal:  J Biol Chem       Date:  2013-07-08       Impact factor: 5.157

8.  Intersubunit cross-talk in pyridoxal 5'-phosphate synthase, coordinated by the C terminus of the synthase subunit.

Authors:  Thomas Raschle; Davide Speziga; Wolfgang Kress; Cyril Moccand; Peter Gehrig; Nikolaus Amrhein; Eilika Weber-Ban; Teresa B Fitzpatrick
Journal:  J Biol Chem       Date:  2008-12-14       Impact factor: 5.157

9.  Slippery substrates impair function of a bacterial protease ATPase by unbalancing translocation versus exit.

Authors:  Priscilla Hiu-Mei Too; Jenny Erales; Joana Danica Simen; Antonija Marjanovic; Philip Coffino
Journal:  J Biol Chem       Date:  2013-03-25       Impact factor: 5.157

10.  Synchrotron protein footprinting supports substrate translocation by ClpA via ATP-induced movements of the D2 loop.

Authors:  Jen Bohon; Laura D Jennings; Christine M Phillips; Stuart Licht; Mark R Chance
Journal:  Structure       Date:  2008-08-06       Impact factor: 5.006

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