Quantitative DNA hybridization in solution using magnetic/luminescent core-shell nanoparticles

被引:50
作者
Son, Ahjeong
Dosev, Dosi
Nichkova, Mikaela
Ma, Zhiya
Kennedy, Ian M.
Scow, Kate M.
Hristova, Krassimira R.
机构
[1] Univ Calif Davis, Dept Land Air & Water Resources, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Mech & Aeronaut Engn, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
关键词
DNA; hybridization-in-solution; nanoparticles; methyl tertiary-butyl ether; lanthanide oxide; magnetic particles;
D O I
10.1016/j.ab.2007.08.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nanoscale magnetic/luminescent core-shell particles were used for DNA quantification in a hybridization-in-solution approach. We demonstrated a rapid, simple, and non-polymerase chain reaction-based DNA hybridization-in-solution assay for quantifying bacteria capable of biodegrading methyl tertiary-butyl ether. Fe3O4/Eu:Gd-2-O-3 core-shell nanoparticles synthesized by spray pyrolysis were biofunctionalized with NeutrAvidin. Following immobilization of a biotinylated probe DNA on the particles' surfaces via passive adsorption, target DNA labeled with fluorescein isothiocyanate was hybridized with probe DNA. The hybridized DNA complex was separated from solution with a magnet, while nonhybridized DNA remained in solution. The normalized fluorescence (fluorescein isothiocyanate/ nanoparticles) measured with a spectrofluorometer indicated a linear quantification (R-2 = 0.98) of the target bacterial 16 S rDNA. The rate of hybridization increased concurrently with the target DNA concentration. In addition, this approach differentiated between the signal outputs from perfectly complementary target and two-base mismatched target DNA in a range of concentrations, showing the specificity of the assay and the possibility for environmental applications. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:186 / 194
页数:9
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