适体
SELEX适体技术
微流控
化学
多重位移放大
计算生物学
色谱法
核糖核酸
聚合酶链反应
指数富集配体系统进化
组合化学
分子生物学
核酸
分析物
DNA
生物
纳米技术
DNA提取
生物化学
材料科学
基因
作者
Chao-Jyun Huang,Hsin-I Lin,Shu‐Chu Shiesh,Gwo‐Bin Lee
标识
DOI:10.1016/j.bios.2012.02.024
摘要
The systematic evolution of ligands by exponential enrichment (SELEX) is a screening technique that involves the progressive selection of highly specific ligands via repeated rounds of partition and amplification from a large random pool of nucleic acid sequences. The products of this selection process are called aptamers and are either short single-stranded deoxyribonucleic acid (ssDNA) or ribonucleic acid (RNA) molecules with a high binding affinity to a large variety of target analytes. However, SELEX is a lengthy, labor-intensive, iterative process requiring multiple rounds of extraction and polymerase chain reaction (PCR) amplification. In order to address these problems, this study presents a new integrated microfluidic system consisting of a magnetic bead-based microfluidic SELEX chip and a competitive assay chip to automate the aptamer screening process. More importantly, the selected ssDNA sequences were confirmed to have a high affinity and specificity to the target molecules, using the developed competitive assay chip. With this approach, an aptamer specific to alpha-fetoprotein (AFP), which is a biomarker for liver cancers, has been successfully selected. The screened aptamer was used as a recognition molecule for AFP and has a linear detection range from 12.5 to 800 ng/mL, which was suitable for rapid clinical applications.
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