Literature DB >> 12667450

Proteomic discovery of cellular substrates of the ClpXP protease reveals five classes of ClpX-recognition signals.

Julia M Flynn1, Saskia B Neher, Yong In Kim, Robert T Sauer, Tania A Baker.   

Abstract

ClpXP is a protease involved in DNA damage repair, stationary-phase gene expression, and ssrA-mediated protein quality control. To date, however, only a handful of ClpXP substrates have been identified. Using a tagged and inactive variant of ClpP, substrates of E. coli ClpXP were trapped in vivo, purified, and identified by mass spectrometry. The more than 50 trapped proteins include transcription factors, metabolic enzymes, and proteins involved in the starvation and oxidative stress responses. Analysis of the sequences of the trapped proteins revealed five recurring motifs: two located at the C terminus of proteins, and three N-terminal motifs. Deletion analysis, fusion proteins, and point mutations established that sequences from each motif class targeted proteins for degradation by ClpXP. These results represent a description of general rules governing substrate recognition by a AAA+ family ATPase and suggest strategies for regulation of protein degradation.

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Year:  2003        PMID: 12667450     DOI: 10.1016/s1097-2765(03)00060-1

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  236 in total

Review 1.  The RpoS-mediated general stress response in Escherichia coli.

Authors:  Aurelia Battesti; Nadim Majdalani; Susan Gottesman
Journal:  Annu Rev Microbiol       Date:  2011       Impact factor: 15.500

2.  Latent ClpX-recognition signals ensure LexA destruction after DNA damage.

Authors:  Saskia B Neher; Julia M Flynn; Robert T Sauer; Tania A Baker
Journal:  Genes Dev       Date:  2003-05-01       Impact factor: 11.361

3.  Distinct peptide signals in the UmuD and UmuD' subunits of UmuD/D' mediate tethering and substrate processing by the ClpXP protease.

Authors:  Saskia B Neher; Robert T Sauer; Tania A Baker
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-31       Impact factor: 11.205

4.  Recruitment of a cytoplasmic response regulator to the cell pole is linked to its cell cycle-regulated proteolysis.

Authors:  Kathleen R Ryan; Sarah Huntwork; Lucy Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-29       Impact factor: 11.205

5.  A proteomic approach for the discovery of protease substrates.

Authors:  Andrew J Bredemeyer; Renate M Lewis; James P Malone; Alan E Davis; Julia Gross; R Reid Townsend; Timothy J Ley
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-27       Impact factor: 11.205

6.  Modulating substrate choice: the SspB adaptor delivers a regulator of the extracytoplasmic-stress response to the AAA+ protease ClpXP for degradation.

Authors:  Julia M Flynn; Igor Levchenko; Robert T Sauer; Tania A Baker
Journal:  Genes Dev       Date:  2004-09-15       Impact factor: 11.361

7.  Role of the processing pore of the ClpX AAA+ ATPase in the recognition and engagement of specific protein substrates.

Authors:  Samia M Siddiqui; Robert T Sauer; Tania A Baker
Journal:  Genes Dev       Date:  2004-02-15       Impact factor: 11.361

8.  Crystal structure of Lon protease: molecular architecture of gated entry to a sequestered degradation chamber.

Authors:  Sun-Shin Cha; Young Jun An; Chang Ro Lee; Hyun Sook Lee; Yeon-Gil Kim; Sang Jin Kim; Kae Kyoung Kwon; Gian Marco De Donatis; Jung-Hyun Lee; Michael R Maurizi; Sung Gyun Kang
Journal:  EMBO J       Date:  2010-09-10       Impact factor: 11.598

9.  The YjbH protein of Bacillus subtilis enhances ClpXP-catalyzed proteolysis of Spx.

Authors:  Saurabh K Garg; Sushma Kommineni; Luke Henslee; Ying Zhang; Peter Zuber
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

10.  A trapping approach reveals novel substrates and physiological functions of the essential protease FtsH in Escherichia coli.

Authors:  Kai Westphal; Sina Langklotz; Nikolas Thomanek; Franz Narberhaus
Journal:  J Biol Chem       Date:  2012-10-22       Impact factor: 5.157

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