posted on 2017-04-28, 18:09authored byCameron
L. C. Smith, Anil H. Thilsted, Jonas N. Pedersen, Tomas H. Youngman, Julia C. Dyrnum, Nicolai A. Michaelsen, Rodolphe Marie, Anders Kristensen
The ability to handle
single, free molecules in lab-on-a-chip systems
is key to the development of advanced biotechnologies. Entropic confinement
offers passive control of polymers in nanofluidic systems by locally
asserting a molecule’s number of available conformation states
through structured landscapes. Separately, a range of plasmonic configurations
have demonstrated active manipulation of nano-objects by harnessing
concentrated electric fields. The integration of these two independent
techniques promises a range of sophisticated and complementary functions
to handle, for example, DNA, but numerous difficulties, in particular,
conflicting requirements of channel size, have prevented progress.
Here, we show that metallic V-groove waveguides, embedded in fluidic
nanoslits, form entropic potentials that trap and guide DNA molecules
over well-defined routes while simultaneously promoting photothermal
transport of DNA through the losses of plasmonic modes. The propulsive
forces, assisted by in-coupling to propagating channel plasmon polaritons,
extend along the V-grooves with a directed motion up to ≈0.5
μm·mW–1 away from the input beam and
λ-DNA velocities reaching ≈0.2 μm·s–1·mW–1. The entropic trapping enables the V-grooves
to be flexibly loaded and unloaded with DNA by variation of transverse
fluid flow, a process that is selective to biopolymers versus fixed-shape objects and also allows the technique to address the
challenges of nanoscale interaction volumes. Our self-aligning, light-driven
actuator provides a convenient platform to filter, route, and manipulate
individual molecules and may be realized wholly by wafer-scale fabrication
suitable for parallelized investigation.