基于 DNA Aptamer 量子点的沙西毒素和河豚毒素竞争性侧流测定的初步开发。

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
John G Bruno
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引用次数: 0

摘要

红色量子点(Qdots)竞争性横向流动(LF)检测条的初步概念验证结果表明,Qdots-蛋白质-沙门氏菌毒素(Stx)和-河豚毒素(Ttx)共轭物的竞争性置换作用持续 15 分钟。出于安全考虑,使用牛血清白蛋白(BSA)-Stx 或 -Ttx 共轭物作为分析物,并应用 NIH ImageJ 图像分析时,最佳版本的检测限(LOD)在 1-2 µg 范围内。但是,如果假定 BSA 中只有一个用 Stx 或 Ttx 标记的伯胺需要作为捕获的 "表位",并按 1 µg 毒素-BSA 共轭物的等摩尔重量计算毒素加合物的重量,则 LOD 低至 4.5 ng 毒素。当 BSA-Stx 和 BSA-Ttx 作为分析物交换时,这些原型试纸条在其各自的检测限或接近检测限时没有出现交叉反应,这与文献中公布的这些适配体的特异性和亲和性研究结果一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preliminary Development of DNA Aptamer Quantum Dot-Based Competitive Lateral Flow Assays for Saxitoxin and Tetrodotoxin.

Initial proof-of-concept development of competitive lateral flow (LF) test strips involving red quantum dots (Qdots) is demonstrated with visible confirmation of the competitive displacement of Qdot-protein-saxitoxin (Stx) and -tetrodotoxin (Ttx) conjugates over 15 min. The measured limits of detection (LODs) for the best versions of the assays were in the 1-2 µg range when a bovine serum albumin (BSA)-Stx or -Ttx conjugate was used as the analyte for safety reasons and NIH ImageJ image analysis was applied. However, when one assumes that only one of the primary amines in BSA labeled with Stx or Ttx is needed as the "epitope" for capture and calculates the weight of the toxin adducts on an equal mole basis to that of 1 µg of toxin-BSA conjugate, the LODs are as low as 4.5 ng of toxin. No cross-reactivity was seen for these prototype test strips when BSA-Stx and BSA-Ttx were switched as analytes at or near their respective LODs which is in agreement with published specificity and affinity studies for these aptamers in the literature.

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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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