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Real-time Tracking of DNA Fragment Separation by Smartphone
Published on: June 1, 2017
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Gel-on-a-chip: continuous, velocity-dependent DNA separation using nanoscale lateral displacement
Benjamin H Wunsch1, Sung-Cheol Kim, Stacey M Gifford
1IBM T. J. Watson Research Center, Yorktown Heights, New York 10598, USA. bhwunsch@us.ibm.com kimsung@us.ibm.com.
Lab on a Chip
|March 29, 2019
Summary
Nanoscale deterministic lateral displacement (nanoDLD) arrays fractionate polymers by size. Flow velocity fine-tunes polymer separation, enabling precise DNA fragment separation and concentration.
Area of Science:
- Polymer physics
- Nanofluidics
- Biomolecular engineering
Background:
- Deterministic lateral displacement (DLD) arrays are micro/nanoscale devices used for particle and cell separation.
- Polymers exhibit complex dynamics in fluid flow, influenced by their size, shape, and flow conditions.
- Efficient separation and fractionation of polymers, such as DNA, are crucial for molecular biology and nanotechnology.
Purpose of the Study:
- To investigate polymer trajectory dynamics in a nanoscale deterministic lateral displacement (nanoDLD) array.
- To demonstrate the potential of nanoDLD devices as a continuous polymer fractionation tool.
- To establish optimal conditions for size-selective separation of double-stranded DNA (dsDNA) fragments.
Main Methods:
- Simulating and analyzing the trajectories of polymers advected and diffusing in a pressure-driven flow through a nanoDLD array.
- Utilizing double-stranded DNA (dsDNA) of varying lengths (100-10,000 base pairs) as a model system.
- Developing a phenomenological model to describe polymer trajectory dependence on gap size and flow velocity.
Main Results:
- Polymers follow size- and velocity-dependent trajectories in nanoDLD arrays.
- dsDNA fragments in the 100-10,000 bp range were separated with a resolution of 200 bp.
- Polymer elongation in shear flow leads to decreased trajectory angles with increasing flow velocity.
- Optimal separation conditions were identified, achieving over 75% recovery and 3-fold concentration of dsDNA fragments.
- Flow velocity was shown to be a key parameter for fine-tuning separation efficiency and resolution.
Conclusions:
- nanoDLD devices offer a continuous, size-selective fractionation method for polymers.
- The velocity-dependent behavior of polymer trajectories provides independent control over separation parameters.
- This technique enables precise separation and concentration of DNA fragments, with potential applications in molecular diagnostics and synthetic biology.
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