Fast microscopical dissection of action scenes played by Escherichia coli RNA polymerase

FEBS Lett. 2012 Sep 21;586(19):3187-92. doi: 10.1016/j.febslet.2012.06.033. Epub 2012 Jul 4.

Abstract

Using fast-scanning atomic force microscopy, we directly visualized the interaction of Escherichia coli RNA polymerase (RNAP) with DNA at the scan rate of 1-2 frames per second. The analyses showed that the RNAP can locate the promoter region not only by sliding but also by hopping and/or segmental transfer. Upon the addition of 0.05 mM NTPs to the stalled complex, the RNAP molecule pulled the template DNA uni-directionally at the rates of 15 nucleotides/s on average. The present method is potentially applicable to examine a variety of protein-nucleic acid interactions, especially those involved in the process of gene regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA Primers / genetics
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / genetics
  • DNA, Bacterial / metabolism
  • DNA, Bacterial / ultrastructure
  • DNA-Directed RNA Polymerases / chemistry
  • DNA-Directed RNA Polymerases / metabolism*
  • DNA-Directed RNA Polymerases / ultrastructure
  • Escherichia coli / enzymology
  • Escherichia coli / genetics
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / metabolism*
  • Escherichia coli Proteins / ultrastructure
  • Microscopy, Atomic Force / methods
  • Promoter Regions, Genetic

Substances

  • DNA Primers
  • DNA, Bacterial
  • Escherichia coli Proteins
  • DNA-Directed RNA Polymerases