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用于复杂介质中甲基膦酸直接分析的量子点 - DNA 荧光共振能量转移共轭物

Quantum Dot-DNA FRET Conjugates for Direct Analysis of Methylphosphonic Acid in Complex Media.

作者信息

Demers Steven M E, Kuhne Wendy W, Swindle Ashlee R, Dick Don D, Coopersmith Kaitlin J

机构信息

Global Security Directorate, Savannah River National Laboratory, P.O. Box A, Aiken, South Carolina 29808, United States.

出版信息

ACS Omega. 2023 Jun 9;8(25):23017-23023. doi: 10.1021/acsomega.3c02173. eCollection 2023 Jun 27.

Abstract

Rapid detection of nerve agents from complex matrices with minimal sample preparation is essential due to their high toxicity and bioavailability. In this work, quantum dots (QDs) were functionalized with oligonucleotide aptamers that specifically targeted a nerve agent metabolite, methylphosphonic acid (MePA). These QD-DNA bioconjugates were covalently linked to quencher molecules to form Förster resonance energy transfer (FRET) donor-acceptor pairs that quantitatively measure the presence of MePA. Using the FRET biosensor, the MePA limit of detection was 743 nM in artificial urine. A decrease in the QD lifetime was measured upon DNA binding and was recovered with MePA. The biosensor's flexible design makes it a strong candidate for the rapid detection of chemical and biological agents for deployable, in-field detectors.

摘要

由于神经毒剂具有高毒性和生物利用度,因此从复杂基质中快速检测神经毒剂且样品制备最少至关重要。在这项工作中,量子点(QDs)用寡核苷酸适配体进行功能化,这些适配体特异性靶向神经毒剂代谢物甲基膦酸(MePA)。这些量子点 - 脱氧核糖核酸生物共轭物与猝灭分子共价连接,形成福斯特共振能量转移(FRET)供体 - 受体对,用于定量测量MePA的存在。使用FRET生物传感器,在人工尿液中MePA的检测限为743 nM。在DNA结合时测量到量子点寿命降低,而与MePA结合后恢复。该生物传感器的灵活设计使其成为用于可部署的现场探测器快速检测化学和生物制剂的有力候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be4/10308513/d30b30afd643/ao3c02173_0002.jpg

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