Single and multiple molecular beacon probes for DNA hybridization studies on a silica glass surface

被引:2
作者
Fang, XH [1 ]
Liu, XJ [1 ]
Tan, WH [1 ]
机构
[1] Univ Florida, Dept Chem, Gainesville, FL 32601 USA
来源
ADVANCES IN FLUORESCENCE SENSING TECHNOLOGY IV, PROCEEDINGS OF | 1999年 / 3602卷
关键词
surface immobilization; molecular beacon; fluorescence; DNA hybridization; DNA probe; biosensors; multiple analytes; silica surface;
D O I
10.1117/12.347516
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Surface immobilizable molecular beacons have been developed for DNA hybridization studies on a silica glass plate. Molecular beacons are a new class of oligonucleotide probes that have a loop-and-stem structure with a fluorophore and a quencher attached to the two ends of the stem. They only emit intense fluorescence when hybridize to their target molecules. This provides an excellent selectivity for the detection of DNA molecules. We have designed biotinylated molecular beacons which can be immobilized onto a solid surface. The molecular beacon is synthesized using DABCYL as the quencher and an optical stable dye, tetramethylrhodamine, as the fluorophore. Mass spectrometry is used to confirm the synthesized molecular beacon. The molecular beacons have been immobilized onto a silica surface through biotin-avidin binding. The surface immobilized molecular beacons have been used for the detection of target DNA with subnanomolar analytical sensitivity. We have also immobilized two different molecular beacons on a silica surface in spatially resolved microscopic regions. The hybridization study of these two different molecular beacon probes has shown excellent selectivity for their target sequences. The newly designed molecular beacons are intended for DNA molecular interaction studies at an interface and for the development of ultrasensitive DNA sensors for a variety of applications including disease diagnosis, disease mechanism studies, new drug development, and in the investigation of molecular interactions between DNA molecules and other interesting biomolecules.
引用
收藏
页码:149 / 155
页数:7
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