High-sensitivity detection of DNA hybridization on microarrays using resonance light scattering

被引:170
作者
Bao, P
Frutos, AG
Greef, C
Lahiri, J [1 ]
Muller, U
Peterson, TC
Warden, L
Xie, XY
机构
[1] Corning Inc, Biochem Technol, Div Sci & Technol, Corning, NY 14831 USA
[2] Genicon Sci Corp, San Diego, CA 92121 USA
关键词
D O I
10.1021/ac0111964
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The application of resonance light scattering (RLS) particles for high-sensitivity detection of DNA hybridization on cDNA microarrays is demonstrated. Arrays composed of similar to2000 human genes ("targets") were hybridized with colabeled (Cy3 and biotin) human lung cDNA probes at concentrations ranging from 8.3 ng/muL to 16.7 pg/muL. After hybridization, the arrays were imaged using a fluorescence scanner. The arrays were then treated with 80-nm-diameter gold RLS Particles coated with anti-biotin antibodies and imaged in a white light, CCD-based imaging system. At low probe concentrations, significantly more genes were detected by RLS compared to labeling by Cy3. For example, for hybridizations with a probe concentration of 83.3 pg/muL, similar to 1150 positive genes were detected using RLS compared to similar to110 positive genes detected with Cy3. In a differential gene expression experiment using human lung and leukemia RNA samples, similar differential expression profiles were obtained for labeling by RLS and fluorescence technologies. The use of RLS Particles is particularly attractive for detection and identification of low-abundance mRNAs and for those applications in which the amount of sample is limited.
引用
收藏
页码:1792 / 1797
页数:6
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