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用于特定核酸检测的量子点介导的生物传感分析

Quantum dot-mediated biosensing assays for specific nucleic acid detection.

作者信息

Yeh Hsin-Chih, Ho Yi-Ping, Wang Tza-Huei

机构信息

Johns Hopkins University, Baltimore, Maryland 21218, USA.

出版信息

Nanomedicine. 2005 Jun;1(2):115-21. doi: 10.1016/j.nano.2005.03.004.

Abstract

Two new classes of quantum dot (QD)-mediated biosensing methods have been developed to detect specific DNA sequences in a separation-free format. Both methods use 2 target-specific oligonucleotide probes to recognize a specific target. The first method is based on cross-linking of 2 QDs with distinct emission wavelengths caused by probe-target hybridization. The second method uses QDs as both fluorescent tags and nanoscaffolds that capture multiple fluorescently labeled hybridization products, resulting in amplified target signals. The presence of targets is determined according to spatiotemporal coincidence of 2 different wavelength fluorescent signals emitted from the QD/DNA/probe complexes. With a single wavelength-excitation, dual wavelength-emission confocal spectroscopic system, the fluorescent signals can be measured with single-dot/molecule sensitivity. Compared with other nanoparticle-based, separation-free assays, our method shows advantages in simplicity, testing speed, and multiplexed applications.

摘要

已经开发出两类新型的量子点(QD)介导的生物传感方法,用于以无分离形式检测特定DNA序列。这两种方法都使用2种靶标特异性寡核苷酸探针来识别特定靶标。第一种方法基于由探针-靶标杂交引起的具有不同发射波长的2个量子点的交联。第二种方法使用量子点作为荧光标签和纳米支架,捕获多个荧光标记的杂交产物,从而放大靶标信号。根据从量子点/DNA/探针复合物发出的2种不同波长荧光信号的时空重合来确定靶标的存在。使用单波长激发、双波长发射共聚焦光谱系统,可以以单点/单分子灵敏度测量荧光信号。与其他基于纳米颗粒的无分离检测方法相比,我们的方法在简单性、检测速度和多重应用方面具有优势。

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