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利用葡萄糖氧化酶和三链DNA识别HIV-1双链DNA的灵敏荧光传感器

Sensitive Fluorescent Sensor for Recognition of HIV-1 dsDNA by Using Glucose Oxidase and Triplex DNA.

作者信息

Li Yubin, Liu Sheng, Ling Liansheng

机构信息

College of Chemistry and Environment, Guangdong Ocean University, Zhanjiang 524088, China.

School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.

出版信息

J Anal Methods Chem. 2018 Apr 1;2018:8298365. doi: 10.1155/2018/8298365. eCollection 2018.

Abstract

A sensitive fluorescent sensor for sequence-specific recognition of double-stranded DNA (dsDNA) was developed on the surface of silver-coated glass slide (SCGS). Oligonucleotide-1 (Oligo-1) was designed to assemble on the surface of SCGS and act as capture DNA, and oligonucleotide-2 (Oligo-2) was designed as signal DNA. Upon addition of target HIV-1 dsDNA (Oligo-3•Oligo-4), signal DNA could bind on the surface of silver-coated glass because of the formation of C•GoC in parallel triplex DNA structure. Biotin-labeled glucose oxidase (biotin-GOx) could bind to signal DNA through the specific interaction of biotin-streptavidin, thereby GOx was attached to the surface of SCGS, which was dependent on the concentration of target HIV-1 dsDNA. GOx could catalyze the oxidation of glucose and yield HO, and the HPPA can be oxidized into a fluorescent product in the presence of HRP. Therefore, the concentration of target HIV-1 dsDNA could be estimated with fluorescence intensity. Under the optimum conditions, the fluorescence intensity was proportional to the concentration of target HIV-1 dsDNA over the range of 10 pM to 1000 pM, the detection limit was 3 pM. Moreover, the sensor had good sequence selectivity and practicability and might be applied for the diagnosis of HIV disease in the future.

摘要

一种用于双链 DNA(dsDNA)序列特异性识别的灵敏荧光传感器在镀银玻片(SCGS)表面构建而成。寡核苷酸 -1(Oligo -1)被设计组装在 SCGS 表面并作为捕获 DNA,寡核苷酸 -2(Oligo -2)被设计为信号 DNA。加入目标 HIV -1 dsDNA(Oligo -3•Oligo -4)后,由于平行三链 DNA 结构中 C•GoC 的形成,信号 DNA 能够结合在镀银玻璃表面。生物素标记的葡萄糖氧化酶(生物素 -GOx)可通过生物素 -链霉亲和素的特异性相互作用与信号 DNA 结合,从而使 GOx 附着在 SCGS 表面,这取决于目标 HIV -1 dsDNA 的浓度。GOx 可催化葡萄糖氧化并产生 H₂O₂,在辣根过氧化物酶(HRP)存在下,HPPA 可被氧化为荧光产物。因此,可通过荧光强度估算目标 HIV -1 dsDNA 的浓度。在最佳条件下,荧光强度在 10 pM 至 1000 pM 范围内与目标 HIV -1 dsDNA 的浓度成正比,检测限为 3 pM。此外,该传感器具有良好的序列选择性和实用性,未来可能应用于 HIV 疾病的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98d5/5901486/7ab0ba81f502/JAMC2018-8298365.001.jpg

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