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在单分子水平监测分子信标DNA探针杂交。

Monitoring molecular beacon DNA probe hybridization at the single-molecule level.

作者信息

Yao Gang, Fang Xiaohong, Yokota Hiroaki, Yanagida Toshio, Tan Weihong

机构信息

Center for Research at the Interface of Bio/nano, Department of Chemistry and the McKnight Brain Institute, University of Florida, Gainesville, FL 32611, USA.

出版信息

Chemistry. 2003 Nov 21;9(22):5686-92. doi: 10.1002/chem.200304977.

DOI:10.1002/chem.200304977
PMID:14639652
Abstract

We have monitored the reaction dynamics of the DNA hybridization process on a liquid/solid interface at the single-molecule level by using a hairpin-type molecular beacon DNA probe. Fluorescence images of single DNA probes were recorded by using total internal reflection fluorescence microscopy. The fluorescence signal of single DNA probes during the hybridization to individual complementary DNA probes was monitored over time. Among 400 molecular beacon DNA probes that we tracked, 349 molecular beacons (87.5 %) were hybridized quickly and showed an abrupt fluorescence increase, while 51 probes (12.5 %) reacted slowly, resulting in a gradual fluorescence increase. This ratio stayed about the same when varying the concentrations of cDNA in MB hybridization on the liquid/surface interface. Statistical data of the 51 single-molecule hybridization images showed that there was a multistep hybridization process. Our results also showed that photostability for the dye molecules associated with the double-stranded hybrids was better than that for those with the single-stranded molecular beacon DNA probes. Our results demonstrate the ability to obtain a better understanding of DNA hybridization processes using single-molecule techniques, which will improve biosensor and biochip development where surface-immobilized molecular beacon DNA probes provide unique advantages in signal transduction.

摘要

我们使用发夹型分子信标DNA探针,在单分子水平上监测了液/固界面上DNA杂交过程的反应动力学。通过全内反射荧光显微镜记录单个DNA探针的荧光图像。随着时间的推移,监测单个DNA探针与单个互补DNA探针杂交过程中的荧光信号。在我们追踪的400个分子信标DNA探针中,349个分子信标(87.5%)快速杂交,荧光急剧增加,而51个探针(12.5%)反应缓慢,导致荧光逐渐增加。在液/表面界面上进行MB杂交时,改变cDNA浓度,该比例基本保持不变。51个单分子杂交图像的统计数据表明存在多步杂交过程。我们的结果还表明,与双链杂交体相关的染料分子的光稳定性优于与单链分子信标DNA探针相关的染料分子。我们的结果证明了使用单分子技术能够更好地理解DNA杂交过程,这将改善生物传感器和生物芯片的开发,其中表面固定的分子信标DNA探针在信号转导方面具有独特优势。

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