Local Hybridization Chain-Reactions

A majority of enzyme-free DNA hybridization reactions in DNA-based molecular systems are limited by the diffusion process - the reaction rates occur faster in the presence of high concentration of reactants, and vice versa. However spurious/unintended interactions are found to be correlated with high concentration of reactants. A solution to reduce spurious interactions is to decrease the concentration of the reactants; however, the hybridization reaction rates, due to the diffusion limitation, take longer for the reactions to complete. Because spurious interactions mitigate the overall functionalities of the DNA-based molecular systems, we propose an alternative method (a follow-up work to Chandran et. al. in 2011) to reduce the interactions. By directly performing the DNA hybridization reactions on fixed nanoscale substrates instead of free-floating in solutions, we conjecture that the spurious interactions are reduced due to spatial locality. This method is expected to achieve minimal spurious interactions and fast DNA hybridization reaction rates.

Instruments & Techniques

  • Transmission electron microscopy
  • DNA quantifications
  • Electroelution
  • Agarose and polyacrylamide gel electrophoresis
  • Agilent (formerly Varian) Eclipse Fluorescence Spectrophotometer
  • Ensemble fluorescence spectroscopy
  • Fluorescence kinetics
  • Bruker (formerly Veeco) Atomic Force Microscope Multimode
  • Tapping in fluid mode
  • Tapping in air mode (AC mode)
  • Alpha Innotech FluoroChem Q MultiImage III
  • Multicolor fluorescence imaging
  • Chemiluminescence
  • Nikon Inverted Microscope
  • LakeShore Cryogenic Probe Station
  • Keithley 4200-SCS Semiconductor Characterization System
  • Agilent 4156C Precision Semiconductor Parameter Analyzer
  • Agilent 4284A Precision LCR Meter

  • Software

  • Mathematica, Matlab, Maple
  • Java, R, EndNote, LaTex, MacPyMol
  • Inkscape, Gimp, Cadnano, ChemBioDraw