袁景利Jingli Yuan

(研究员)

 博士生导师  硕士生导师
学位:博士
性别:男
毕业院校:早稻田大学
所在单位:化学学院
电子邮箱:jlyuan@dlut.edu.cn

论文成果

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Design of a Room-Temperature Phosphorescence-Based Molecular Beacon for Highly Sensitive Detection of Nucleic Acids in Biological Fluids

发表时间:2019-03-09 点击次数:

论文名称:Design of a Room-Temperature Phosphorescence-Based Molecular Beacon for Highly Sensitive Detection of Nucleic Acids in Biological Fluids
论文类型:期刊论文
发表刊物:ANALYTICAL CHEMISTRY
收录刊物:SCIE、EI
卷号:83
期号:4
页面范围:1356-1362
ISSN号:0003-2700
摘要:Ultrasensitive fluorescent analysis or monitoring of significant molecules in complex samples is important for many biological studies, clinical diagnosis, and forensic investigations, the major obstacle for which is the background signals from ubiquitous endogenous fluorescent components of the environments. Herein, a room-temperature Phosphorescence (RTP)based molecular beacon (MB), employing a Eu(3+) complex of chlorosulfonylated tetradentate beta-diketone (L) and the quencher BHQ-2, was engineered for highly sensitive detection of DNA sequences in biological fluids. Complexation of Eu(3+). with the ligand L formed a strongly luminescent complex EuL(2). But when EuL(2) and BHQ-2 were labeled to two ends of a DNA molecule with hairpin structure, the luminescence of EuL(2) was quenched by BHQ-2 due to the stem-closed conformation of the beacon. Due to very low background luminescence from the probe molecule, >200-fold signal enhancement was achieved when nanomolar target sequence was introduced. This sensitivity is about 20-fold higher than the level achieved with conventional fluorescence-based molecular beacons. Furthermore, because the Eu(3+) complex has a much longer luminescence lifetime (approximate to 0.8 ms) than that of the background (<10 ns), RTP measurements were used to directly detect as low as 500 pM DNA in cell media quantitatively without any sample pretreatment.
发表时间:2011-02-15