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Structure and function of ClpXP, a AAA+ proteolytic machine powered by probabilistic ATP hydrolysis.

Robert T SauerXue FeiTristan A BellTania A Baker
Published in: Critical reviews in biochemistry and molecular biology (2021)
ClpXP is an archetypical AAA+ protease, consisting of ClpX and ClpP. ClpX is an ATP-dependent protein unfoldase and polypeptide translocase, whereas ClpP is a self-compartmentalized peptidase. ClpXP is currently the only AAA+ protease for which high-resolution structures exist, the molecular basis of recognition for a protein substrate is understood, extensive biochemical and genetic analysis have been performed, and single-molecule optical trapping has allowed direct visualization of the kinetics of substrate unfolding and translocation. In this review, we discuss our current understanding of ClpXP structure and function, evaluate competing sequential and probabilistic mechanisms of ATP hydrolysis, and highlight open questions for future exploration.
Keyphrases
  • single molecule
  • high resolution
  • amino acid
  • protein protein
  • atomic force microscopy
  • minimally invasive
  • anaerobic digestion
  • binding protein
  • mass spectrometry
  • deep learning
  • machine learning
  • tandem mass spectrometry