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Dynamics and stoichiometry of a regulated enhancer-binding protein in live Escherichia coli cells

Author

Listed:
  • Parul Mehta

    (Imperial College London)

  • Goran Jovanovic

    (Imperial College London)

  • Tchern Lenn

    (Imperial College London
    Present address: Lawrence Berkeley National laboratory, University of California, Berkeley, USA)

  • Andreas Bruckbauer

    (Lymphocyte Interaction Laboratory, London Research Institute, Cancer Research UK)

  • Christoph Engl

    (Imperial College London
    Present address: Skirball Institute of Biomolecular Medicine, New York University Medical School, New York, USA)

  • Liming Ying

    (Faculty of Medicine, Molecular Medicine, National Heart and Lung Institute, Imperial College London)

  • Martin Buck

    (Imperial College London)

Abstract

Bacterial enhancer-dependent transcription systems support major adaptive responses and offer a singular paradigm in gene control analogous to complex eukaryotic systems. Here we report new mechanistic insights into the control of one-membrane stress-responsive bacterial enhancer-dependent system. Using millisecond single-molecule fluorescence microscopy of live cells we determine the localizations, two-dimensional diffusion dynamics and stoichiometries of complexes of the bacterial enhancer-binding ATPase PspF during its action at promoters as regulated by inner membrane interacting negative controller PspA. We establish that a stable repressive PspF–PspA complex is located in the nucleoid, transiently communicating with the inner membrane via PspA. The PspF as a hexamer stably binds only one of the two psp promoters at a time, suggesting that psp promoters will fire asynchronously and cooperative interactions of PspF with the basal transcription complex influence dynamics of the PspF hexamer–DNA complex and regulation of the psp promoters.

Suggested Citation

  • Parul Mehta & Goran Jovanovic & Tchern Lenn & Andreas Bruckbauer & Christoph Engl & Liming Ying & Martin Buck, 2013. "Dynamics and stoichiometry of a regulated enhancer-binding protein in live Escherichia coli cells," Nature Communications, Nature, vol. 4(1), pages 1-9, October.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2997
    DOI: 10.1038/ncomms2997
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