Application of supramolecular nanostamping to the replication of DNA nanoarrays

The rapid development of molecular biology is creating a pressing need for arrays of biomolecules that are able to detect smaller and smaller volumes of analytes. This goal can be achieved by shrinking the average size and spacing of the arrays constituent features. While bioarrays with dot size and spacing on the nanometer scale have been successfully fabricated via scanning probe microscopy-based techniques, such fabrication methods are serial in nature and consequently slow and expensive. Additionally, the development of truly small arrays able to analyze scarce volumes of liquids is hindered by the present use of optical detection, which sets the minimum dot spacing on the order of roughly half the excitation wavelength. Here, we show that supramolecular nanostamping, a recently introduced truly parallel method for the stamping of DNA features, can efficiently reproduce DNA arrays with features as small as 14 +/- 2 nm spaced 77 +/- 10 nm. Moreover, we demonstrate that hybridization of these nanoarrays can be detected using atomic force microscopy in a simple and scaleable way that additionally does not require labeling of the DNA strands.
Publisher
Amer Chemical Soc
Issue Date
2007-10
Language
ENG
Keywords

DIP-PEN NANOLITHOGRAPHY; NANOFABRICATION; CLUSTERS; SURFACES; PROBES; ARRAY

Citation

NANO LETTERS, v.7, no.11, pp.3493 - 3498

ISSN
1530-6984
DOI
10.1021/nl0720758
URI
http://hdl.handle.net/10203/7946
Appears in Collection
CBE-Journal Papers(저널논문)
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