Cao Yuan-Cheng, Liu Tian-Cai, Hua Xiao-Feng, Zhu Xiao-Xia, Wang Hai-Qiao, Huang Zhen-Li, Zhao Yuan-Di, Liu Man-Xi, Luo Qing-Ming
Key Laboratory of Biomedical Photonics of Ministry of Education, HuBei Bioinformatics and Molecular Imaging Key Laboratory, Huazhong University of Science and Technology, College of Life Science and Technology, Wuhan, HuBei, China 430074.
J Biomed Opt. 2006 Sep-Oct;11(5):054025. doi: 10.1117/1.2358957.
A novel multiplex analysis technology based on quantum dot (QD) optical encoded beads was studied. Carboxyl functionalized polystyrene beads, about 100 microm in size, were precisely encoded by the various ratios of two types of QDs whose emission wavelengths are 576 and 628 nm, respectively. Then the different encoded beads were covalently immobilized with different probes in the existing of sulfo-NHS and 1-[3-(Dimethylamino) propyl]-3-ethylcarbodiimide methiodide, and the probe density could reach to 3.1 mmol/g. These probe-linked encoded beads were used to detect the target DNA sequences in complex DNA solution by hybridization. Hybridization was visualized using fluorescein isothiocynate-labeled DNA sequences. The results show that the QDs and target signals can be obviously identified from a single-bead-level spectrum. This technology can detect DNA targets effectively with a detection limit of 0.2 microg/mL in complex solution.
研究了一种基于量子点(QD)光学编码微球的新型多重分析技术。尺寸约为100微米的羧基功能化聚苯乙烯微球,通过两种发射波长分别为576纳米和628纳米的量子点的不同比例进行精确编码。然后,在磺基-NHS和1-[3-(二甲氨基)丙基]-3-乙基碳二亚胺甲基碘存在的情况下,将不同编码的微球与不同的探针共价固定,探针密度可达3.1 mmol/g。这些连接了探针的编码微球用于通过杂交检测复杂DNA溶液中的目标DNA序列。使用异硫氰酸荧光素标记的DNA序列对杂交进行可视化。结果表明,从单微球水平光谱中可以明显识别量子点和目标信号。该技术能够在复杂溶液中有效检测DNA目标,检测限为0.2微克/毫升。