Measuring intermolecular rupture forces with a combined TIRF-optical trap microscope and DNA curtains

Biochem Biophys Res Commun. 2012 Oct 5;426(4):565-70. doi: 10.1016/j.bbrc.2012.08.127. Epub 2012 Sep 4.

Abstract

We report a new approach to probing DNA-protein interactions by combining optical tweezers with a high-throughput DNA curtains technique. Here we determine the forces required to remove the individual lipid-anchored DNA molecules from the bilayer. We demonstrate that DNA anchored to the bilayer through a single biotin-streptavidin linkage withstands ∼20pN before being pulled free from the bilayer, whereas molecules anchored to the bilayer through multiple attachment points can withstand ⩾65pN; access to this higher force regime is sufficient to probe the responses of protein-DNA interactions to force changes. As a proof-of-principle, we concurrently visualized DNA-bound fluorescently-tagged RNA polymerase while simultaneously stretching the DNA molecules. This work presents a step towards a powerful experimental platform that will enable concurrent visualization of DNA curtains while applying defined forces through optical tweezers.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • DNA / chemistry*
  • DNA-Directed RNA Polymerases / chemistry
  • Lipid Bilayers / chemistry
  • Microscopy, Fluorescence / methods*
  • Optical Tweezers*
  • Protein Binding
  • Proteins / chemistry*

Substances

  • Lipid Bilayers
  • Proteins
  • DNA
  • DNA-Directed RNA Polymerases