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基于超灵敏量子点的 DNA 检测及与消逝波生物传感平台的杂交动力学分析。

Ultrasensitive quantum dots-based DNA detection and hybridization kinetics analysis with evanescent wave biosensing platform.

机构信息

Environmental Simulation and Pollution Control State Key Joint Laboratory, Department of Environment Science and Engineering, Tsinghua University, Beijing 100084, China.

出版信息

Biosens Bioelectron. 2011 Jan 15;26(5):2390-5. doi: 10.1016/j.bios.2010.10.018. Epub 2010 Oct 16.

Abstract

Ultrasensitive DNA detection was achieved using a new biosensing platform based on quantum dots (QDs) and total internal reflection fluorescence, which featured an exceptional detection limit of 3.2 amol of bound target DNA. The reusable sensor surface was produced by covalently immobilizing streptavidin onto a self-assembled alkanethiol monolayer of fiber optic probe through a heterobifunctional reagent. Streptavidin served as a versatile binding element for biotinylated single-strand DNA (ssDNA). The ssDNA-coated fiber probe was evaluated as a nucleic acid biosensor through a DNA-DNA hybridization assay for a 30-mer ssDNA, which were the segments of the uidA gene of Escherichia coli and labeled by QDs using avidin-biotin interaction. Several negative control tests revealed the absence of significant non-specific binding. It also showed that bound target DNA could easily be eluted from the sensor surface using SDS solution (pH 1.9) without any significant loss of performance after more than 30 assay cycles. A quantitative measurement of DNA binding kinetics was achieved with high accuracy, indicating an association rate of 1.38×10(6) M(-1) s(-1) and a dissociation rate of 4.67×10(-3) s(-1). The proposed biosensing platform provides a simple, cheap, fast, and robust solution for many potential applications including clinical diagnosis, pathology, and genetics.

摘要

基于量子点(QDs)和全内反射荧光的新型生物传感平台实现了超灵敏的 DNA 检测,其检测限达到了 3.2 amol 的结合目标 DNA。通过异双功能试剂将链霉亲和素共价固定在光纤探针的自组装烷硫醇单层上,制备了可重复使用的传感器表面。链霉亲和素是生物素化单链 DNA(ssDNA)的通用结合元件。ssDNA 涂层光纤探针通过 DNA-DNA 杂交测定法作为核酸生物传感器进行了评估,该测定法使用 avidin-biotin 相互作用对 30 个碱基 ssDNA 进行了标记,这些 ssDNA 是大肠杆菌 uidA 基因的片段。通过进行多次阴性对照测试,证实不存在明显的非特异性结合。实验还表明,结合的目标 DNA 可以使用 SDS 溶液(pH 1.9)从传感器表面轻松洗脱,并且在 30 多次测定循环后,性能没有明显下降。通过高精度实现了 DNA 结合动力学的定量测量,表明缔合速率为 1.38×10(6) M(-1) s(-1),解离速率为 4.67×10(-3) s(-1)。该生物传感平台为许多潜在应用提供了一种简单、廉价、快速且稳健的解决方案,包括临床诊断、病理学和遗传学。

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