4.5 Article

Three-dimensional hydrogel structures as optical sensor arrays, for the detection of specific DNA sequences

Journal

ANALYTICAL BIOCHEMISTRY
Volume 421, Issue 1, Pages 1-8

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2011.10.026

Keywords

Hydrogel; Biosensor; Biological assay development; Nanobiotechnology

Funding

  1. Enterprise Ireland [PC-2008-030]
  2. Wellcome Trust [075491/Z/04, p.W1282X, p.F508del]
  3. Electron Microscopy Facility Biosciences Institute in UCC
  4. Higher Education Authority of Ireland

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The fabrication and characterization of surface-attached PEG-diacrylate hydrogel structures and their application as sensing platforms for the detection of specific target sequences are reported. Hydrogel structures were formed by a photopolymerization process, using substrate-bound Eosin Y molecules for the production of free radicals. We have demonstrated that this fabrication process allows for control over hydrogel growth down to the micrometer scale. Confocal imaging revealed relatively large pore structures for 25% (v/v) PEG-diacrylate hydrogels, which appear to lie in tightly packed layers. Our data suggest that these pore structures decrease in size for hydrogels with increasing levels of PEG-diacrylate. Surface coverage values calculated for hydrogels immobilized with 21-mer DNA probe sequences were significantly higher compared to those previously reported for 2- and 3-dimensional sensing platforms, on the order of 10(16) molecules cm(-2). Used as sensing platforms in DNA hybridization assays, a detection limit of 3.9 nM was achieved for hybridization reactions between 21-mer probe and target sequences. The ability of these hydrogel sensing platforms to discriminate between wild-type and mutant allele sequences was also demonstrated, down to target concentrations of 1-2 nM. A reduction in the hybridization time down to a period of 15 min was also achieved, while still maintaining confident results, demonstrating the potential for future integration of these sensing platforms within Lab-on-Chip or diagnostic devices. (C) 2011 Elsevier Inc. All rights reserved.

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