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Keyword
- ATP-dependent protease1
- bovine serum albumin1
- BSA1
- DDS1
- DHFR1
- dichlorodimethylsilane1
- dihydrofolate reductase1
- enzyme kinetics1
- GAr1
- glycine-alanine repeat1
- LCR1
- low complexity region1
- methotrexate1
- MTX1
- polyG1
- polyglycine1
- protein degradation1
- protein sequence1
- single molecule biophysics1
- TIRF1
- total internal reflection fluorescence1
Protein Synthesis and Degradation
1 Results
- Research ArticleOpen Access
Single molecule microscopy reveals diverse actions of substrate sequences that impair ClpX AAA+ ATPase function
Journal of Biological ChemistryVol. 298Issue 10102457Published online: September 2, 2022- Xiao Wang
- Sanford M. Simon
- Philip Coffino
Cited in Scopus: 0AAA+ (ATPases Associated with diverse cellular Activities) proteases unfold substrate proteins by pulling the substrate polypeptide through a narrow pore. To overcome the barrier to unfolding, substrates may require extended association with the ATPase. Failed unfolding attempts can lead to a slip of grip, which may result in substrate dissociation, but how substrate sequence affects slippage is unresolved. Here, we measured single molecule dwell time using total internal reflection fluorescence microscopy, scoring time-dependent dissociation of engaged substrates from bacterial AAA+ ATPase unfoldase/translocase ClpX.