利用末端脱氧核苷酸转移酶在片上扩增信号的微阵列检测病原体基因的方法

IF 4.7 Q2 NANOSCIENCE & NANOTECHNOLOGY Micro and Nano Systems Letters Pub Date : 2022-08-22 DOI:10.1186/s40486-022-00153-8
Tai-Yong Kim, Min-Cheol Lim, Jeong-A Lim, Sung-Wook Choi, Min-Ah Woo
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引用次数: 2

摘要

利用末端脱氧核苷酸转移酶(TdT)在芯片上扩增信号,建立了一种检测致病基因的微阵列检测方法。用氧等离子体处理用于微阵列的环烯烃共聚物(COC)底物,诱导其表面亲水性能。通过紫外照射将捕获探针DNA固定在COC表面。固定在COC表面的捕获探针DNA的3′末端用磷酸基团修饰,以提供对TdT反应的抗性。因此,只有当捕获探针DNA获得目标基因,并在目标基因的3′端连续添加生物素-11-脱氧尿苷三磷酸(b-dUTP)时,才会触发TdT反应。随后,利用生物素-链霉亲和素相互作用,将链霉亲和素共轭金纳米粒子(s-AuNPs)标记在聚尿苷尾部。在s-AuNPs的存在下,视觉信号被银增强放大。通过对四种病原菌的分析和目视鉴定,证实了这种检测方法的有效性。
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Microarray detection method for pathogen genes by on-chip signal amplification using terminal deoxynucleotidyl transferase

A microarray detection method based on on-chip signal amplification using terminal deoxynucleotidyl transferase (TdT) was developed to visualize pathogenic genes. Cyclic olefin copolymer (COC) substrate for microarrays was treated with oxygen plasma to induce hydrophilic surface properties. The capture probe DNA was immobilized on the COC surface by UV irradiation. The 3ʹ end of the capture probe DNA immobilized on the COC surface was modified with a phosphate group to provide resistance against the TdT reaction. Therefore, the TdT reaction was triggered only when the capture probe DNA acquired the target gene, and biotin-11-deoxyuridine triphosphate (b-dUTP) was continuously added to the 3ʹ end of the target gene. Thereafter, streptavidin-conjugated gold nanoparticles (s-AuNPs) tagged the poly uridine tails by the biotin–streptavidin interaction. The visual signal was amplified by silver enhancement in the presence of the s-AuNPs. The usefulness of this detection method was confirmed by analyzing four pathogens and allowing their visual identification.

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来源期刊
Micro and Nano Systems Letters
Micro and Nano Systems Letters Engineering-Biomedical Engineering
CiteScore
10.60
自引率
5.60%
发文量
16
审稿时长
13 weeks
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