Analysis of DNA coverage using enzymatic cleavage of fluorescent labels

Authors
Kim, Mi JungZheng, ShunKim, Tae SongKim, Sang Kyung
Issue Date
2011-03-20
Publisher
SPRINGER
Citation
BIOCHIP JOURNAL, v.5, no.1, pp.39 - 46
Abstract
In this study, a method to determine the degree of DNA coverage on gold surface using a fluorescent dye and Deoxyribonuclease I (DNase I) was developed. Gold surfaces were first functionalized with fluorescent dye labeled DNA, which was followed by DNase T digestion. The number of released fluorescent dyes represented the quantity of DNA immobilized. The use of DNase I to enzymatically cleave the fluorescent dye decreased the time needed for quantification to 1 h. In this way, the effect of a back-filler, DNA concentration, incubation time and spacer on DNA immobilization via gold-thiol chemistry was examined. The concentration of oligonucleotides and the ionic environment were the major factors determining DNA density. We also found that the length of DNA molecule influenced the rate of immobilization on Au. In addition, mixed self-assembled monolayer (mixed-SAM) with various composition and the the effect on DNA density was investigated.
Keywords
SURFACE-PLASMON RESONANCE; HYBRIDIZATION EFFICIENCY; GOLD SURFACES; MONOLAYERS; SPECTROSCOPY; BIOSENSORS; DENSITY; NANOPARTICLES; ADSORPTION; BINDING; SURFACE-PLASMON RESONANCE; HYBRIDIZATION EFFICIENCY; GOLD SURFACES; MONOLAYERS; SPECTROSCOPY; BIOSENSORS; DENSITY; NANOPARTICLES; ADSORPTION; BINDING; DNA quantification; Gold; Biosensor; Deoxyribonuclease I; Fluorescent label
ISSN
1976-0280
URI
https://pubs.kist.re.kr/handle/201004/130520
DOI
10.1007/s13206-011-5107-2
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KIST Article > 2011
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