Dec 10, 2013

Ordered, Random, Monotonic, and Non-monotonic Digital Nanodot Gradients

BioRxiv : the Preprint Server for Biology
Grant OngoDavid Juncker

Abstract

Cell navigation is directed by inhomogeneous distributions of extracellular cues. It is well known that noise plays a key role in biology and is present in naturally occurring gradients at the micro- and nanoscale, yet it has not been studied with gradients in vitro . Here, we introduce novel algorithms to produce ordered and random gradients of discrete nanodots – called digital nanodot gradients (DNGs) – according to monotonic and non-monotonic density functions. The algorithms generate continuous DNGs, with dot spacing changing in two dimensions along the gradient direction according to arbitrary mathematical functions, with densities ranging from 0.02% to 44.44%. The random gradient algorithm compensates for random nanodot overlap, and the randomness and spatial homogeneity of the DNGs were confirmed with Ripley’s K function. An array of 100 DNGs, each 400 × 400 µm2, comprising a total of 57 million 200 × 200 nm2 dots was designed and patterned into silicon using electron-beam lithography, then patterned as fluorescently labeled IgGs on glass using lift-off nanocontact printing. DNGs will facilitate the study of the effects of noise and randomness at the micro- and nanoscales on cell migration and growth.

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Mentioned in this Paper

Teleradiotherapy Using Electrons
Mirafra passerina
Extracellular
Spatial Distribution
Molecular_function
Patient Navigation
OFD1 protein, rat
Migration, Cell
Array
Silicon

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