Disturbance-free rapid solution exchange for magnetic tweezers single-molecule studies

Nucleic Acids Res. 2015 Sep 30;43(17):e113. doi: 10.1093/nar/gkv554. Epub 2015 May 24.

Abstract

Single-molecule manipulation technologies have been extensively applied to studies of the structures and interactions of DNA and proteins. An important aspect of such studies is to obtain the dynamics of interactions; however the initial binding is often difficult to obtain due to large mechanical perturbation during solution introduction. Here, we report a simple disturbance-free rapid solution exchange method for magnetic tweezers single-molecule manipulation experiments, which is achieved by tethering the molecules inside microwells (typical dimensions-diameter (D): 40-50 μm, height (H): 100 μm; H:D∼2:1). Our simulations and experiments show that the flow speed can be reduced by several orders of magnitude near the bottom of the microwells from that in the flow chamber, effectively eliminating the flow disturbance to molecules tethered in the microwells. We demonstrate a wide scope of applications of this method by measuring the force dependent DNA structural transitions in response to solution condition change, and polymerization dynamics of RecA on ssDNA/SSB-coated ssDNA/dsDNA of various tether lengths under constant forces, as well as the dynamics of vinculin binding to α-catenin at a constant force (< 5 pN) applied to the α-catenin protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA / chemistry
  • DNA, Single-Stranded / metabolism
  • DNA-Binding Proteins / metabolism
  • Microfluidic Analytical Techniques*
  • Rec A Recombinases / metabolism
  • Sodium Chloride
  • Vinculin / metabolism
  • alpha Catenin / metabolism

Substances

  • DNA, Single-Stranded
  • DNA-Binding Proteins
  • alpha Catenin
  • Vinculin
  • Sodium Chloride
  • DNA
  • Rec A Recombinases