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基于截短适配体-二硫化钼纳米片信号增强免标记荧光检测金刚烷胺OA北大核心CSTPCD

Detection of Amantadine by Label-free Fluorescence Method Based on Truncated Aptamer and Molybdenum Disulfide Nanosheet Signal Enhancement Strategy

中文摘要英文摘要

金刚烷胺(AMD)可与其核酸适配体特异性结合,导致构象由单链转换成茎环结构.为避免多余的核苷酸影响适配体与靶标结合形成复杂的空间结构,本研究通过保留适当的茎环结构对AMD原适配体J进行截短优化,开发出新的截短适配体.与原适配体相比,截短适配体J-7与AMD的亲和力和特异性更好.以J-7为特异性识别元件,结合二硫化钼纳米片(MoS2Ns)信号放大技术构建了一种基于核酸适配体-MoS2Ns的超灵敏免标记荧光法用于AMD的检测,检出限为0.11 ng/mL.将本方法用于实际牛奶、酸奶及SD大鼠血清样品中AMD的检测,回收率为86.6%~108.2%.本研究为其它长序列适配体的截短提供了参考依据,也为食品中AMD残留的检测提供了更灵敏的检测方法.

Amantadine(AMD)residue can accumulate in organisms through the food chain and cause serious harm to human body.AMD can specifically bind to AMD specific aptamer and cause its conformation to change from a random single strand to a stem-loop structure.To avoid the influence of excess nucleotides on binding of aptamer to AMD,the truncation of the AMD original aptamer J was optimized by retaining an appropriate stem-loop structure,and a new type of truncation aptamers was developed in this work.By comparing the truncated aptamer with the original aptamer,it was found that the truncated aptamer J-7 had better affinity and specificity with AMD.The detection limit of AMD was 0.11 ng/mL by using J-7 as specific recognition element and molybdenum disulfide nanosheet(MoS2Ns)as signal amplification element.The developed method base on truncated aptamer J-7 was used for detection of AMD in milk,yogurt and SD rat serum samples for the first time with recoveries of 86.6%-108.2%.This study provided a reference for truncating other long sequence aptamers and provided a more sensitive detection method for monitoring AMD residues in food.

兰艺凤;侯博雅;尉志文;刘文;张潮;左雅慧;贠克明

山西医科大学法医学院,晋中 030600山西医科大学基础医学院,晋中 030600中国辐射防护研究院,太原 030000

截短适配体二硫化钼纳米片信号增强金刚烷胺免标记荧光法

Truncated aptamerMolybdenum disulfide nanosheetSignal enhancementAmantadineLabel-free fluorescence sensing system

《分析化学》 2024 (002)

208-219,中插4-中插7 / 16

国家自然科学基金项目(No.82202083)和山西省自然科学基金项目(No.20210302124290)资助.Supported by the National Natural Science Foundation of China(No.82202083)and the Natural Science Foundation of Shanxi Province,China(No.20210302124290).

10.19756/j.issn.0253-3820.231127

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