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Hybridization chain reaction amplification for highly sensitive fluorescence detection of DNA with dextran coated microarrays

DNA微阵列 荧光 聚合酶链反应 DNA 多重位移放大 连锁反应 化学 杂交探针 核酸热力学 DNA–DNA杂交 荧光原位杂交 右旋糖酐 分子生物学 DNA提取 色谱法 生物 基序列 生物化学 基因 光化学 基因表达 物理 量子力学 染色体
作者
Jie Chao,Zhenhua Li,Jing Li,Hongzhen Peng,Shao Su,Qian Li,Chengfeng Zhu,Xiaolei Zuo,Shiping Song,Lianhui Wang,Lihua Wang
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:81: 92-96 被引量:31
标识
DOI:10.1016/j.bios.2016.01.093
摘要

Microarrays of biomolecules hold great promise in the fields of genomics, proteomics, and clinical assays on account of their remarkably parallel and high-throughput assay capability. However, the fluorescence detection used in most conventional DNA microarrays is still limited by sensitivity. In this study, we have demonstrated a novel universal and highly sensitive platform for fluorescent detection of sequence specific DNA at the femtomolar level by combining dextran-coated microarrays with hybridization chain reaction (HCR) signal amplification. Three-dimensional dextran matrix was covalently coated on glass surface as the scaffold to immobilize DNA recognition probes to increase the surface binding capacity and accessibility. DNA nanowire tentacles were formed on the matrix surface for efficient signal amplification by capturing multiple fluorescent molecules in a highly ordered way. By quantifying microscopic fluorescent signals, the synergetic effects of dextran and HCR greatly improved sensitivity of DNA microarrays, with a detection limit of 10fM (1×10(5) molecules). This detection assay could recognize one-base mismatch with fluorescence signals dropped down to ~20%. This cost-effective microarray platform also worked well with samples in serum and thus shows great potential for clinical diagnosis.

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