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


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.

SUBMITTER: Lee JY 

PROVIDER: S-EPMC3467351 | biostudies-literature | 2012 Oct

REPOSITORIES: biostudies-literature

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

Lee Ja Yil JY   Wang Feng F   Fazio Teresa T   Wind Shalom S   Greene Eric C EC  

Biochemical and biophysical research communications 20120904 4


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; a  ...[more]

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