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磁性粒子和量子点探针上核酸杂交的定量分析。

Quantitative analysis of nucleic Acid hybridization on magnetic particles and quantum dot-based probes.

机构信息

Diagnostics, Institut Pasteur Korea, 696 Sampyeong-dong, Bundang-gu, Seongnam City, Gyeonggi-do, Korea, 443-270.

出版信息

Sensors (Basel). 2009;9(7):5590-9. doi: 10.3390/s90705590. Epub 2009 Jul 14.

Abstract

In the present study we describe sandwich design hybridization probes consisting of magnetic particles (MP) and quantum dots (QD) with target DNA, and their application in the detection of avian influenza virus (H5N1) sequences. Hybridization of 25-, 40-, and 100-mer target DNA with both probes was analyzed and quantified by flow cytometry and fluorescence microscopy on the scale of single particles. The following steps were used in the assay: (i) target selection by MP probes and (ii) target detection by QD probes. Hybridization efficiency between MP conjugated probes and target DNA hybrids was controlled by a fluorescent dye specific for nucleic acids. Fluorescence was detected by flow cytometry to distinguish differences in oligo sequences as short as 25-mer capturing in target DNA and by gel-electrophoresis in the case of QD probes. This report shows that effective manipulation and control of micro- and nanoparticles in hybridization assays is possible.

摘要

在本研究中,我们描述了由磁性颗粒 (MP) 和量子点 (QD) 与目标 DNA 组成的夹心设计杂交探针,并将其应用于禽流感病毒 (H5N1) 序列的检测。通过在单颗粒尺度上的流式细胞术和荧光显微镜分析和定量了 25 、 40 和 100 -mer 目标 DNA 与两种探针的杂交。该测定法包括以下步骤:(i)通过 MP 探针选择目标,(ii)通过 QD 探针检测目标。与目标 DNA 杂交的 MP 缀合探针之间的杂交效率通过专门针对核酸的荧光染料来控制。通过流式细胞术检测荧光以区分目标 DNA 中短至 25-mer 捕获的寡核苷酸序列的差异,并且在 QD 探针的情况下通过凝胶电泳进行区分。本报告表明,在杂交测定中可以有效地操作和控制微球和纳米颗粒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/3274159/5ddd566d572d/sensors-09-05590f1.jpg

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