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基于光捕获 FRET 的纳米探针的智能手机辅助核酸检测。

Smartphone-assisted detection of nucleic acids by light-harvesting FRET-based nanoprobe.

机构信息

Laboratoire de Biophotonique et Pathologies, Faculté de Pharmacie, UMR 7021, CNRS, Université de Strasbourg, 74, Route du Rhin, 67401, Cedex, Illkirch, France.

Laboratoire de Biophotonique et Pathologies, Faculté de Pharmacie, UMR 7021, CNRS, Université de Strasbourg, 74, Route du Rhin, 67401, Cedex, Illkirch, France.

出版信息

Biosens Bioelectron. 2020 Nov 15;168:112515. doi: 10.1016/j.bios.2020.112515. Epub 2020 Aug 15.

DOI:10.1016/j.bios.2020.112515
PMID:32862092
Abstract

Point-of-care assays for optical detection of biomolecular markers attract growing attention, because of their capacity to provide rapid and inexpensive diagnostics of cancer and infectious diseases. Here, we designed a nanoprobe compatible with a smartphone RGB camera for detection of nucleic acids. It is based on light-harvesting polymeric nanoparticles (NPs) encapsulating green fluorescent donor dyes that undergo efficient Förster Resonance Energy Transfer (FRET) to red fluorescent acceptor hybridized at the particle surface. Green-emitting NPs are based on rhodamine 110 and 6G dyes paired with bulky hydrophobic counterions, which prevent dye self-quenching and ensure efficient energy transfer. Their surface is functionalized with a capture DNA sequence for cancer marker survivin, hybridized with a short oligonucleotide bearing FRET acceptor ATTO647N. Obtained 40-nm poly(methyl methacrylate)-based NP probe, encapsulating octadecyl rhodamine 6G dyes with tetrakis(perfluoro-tert-butoxy)aluminate counterions (~6000 dyes per NP), and bearing 65 acceptors, shows efficient FRET with >20% quantum yield and a signal amplification (antenna effect) of 25. It exhibits ratiometric response to the target DNA by FRET acceptor displacement and enables DNA detection in solution by fluorescence spectroscopy (limit of detection 3 pM) and on surfaces at the single-particle level using two-color fluorescence microscopy. Using a smartphone RGB camera, the nanoprobe response can be readily detected at 10 pM target in true color and in red-to-green ratio images. Thus, our FRET-based nanoparticle biosensor enables detection of nucleic acid targets using a smartphone coupled to an appropriate optical setup, opening the way to simple and inexpensive point-of-care assays.

摘要

即时检测光学生物标志物的分析方法因其能够快速、廉价地诊断癌症和传染病而受到越来越多的关注。在这里,我们设计了一种与智能手机 RGB 摄像头兼容的纳米探针,用于检测核酸。它基于光收集聚合物纳米粒子(NPs),其中封装了绿色荧光供体染料,这些染料通过高效Förster 共振能量转移(FRET)与粒子表面杂交的红色荧光受体发生作用。绿色发射 NPs 基于罗丹明 110 和 6G 染料与庞大的疏水性抗衡离子配对,这可以防止染料自猝灭并确保有效的能量转移。它们的表面用用于癌症标志物生存素的捕获 DNA 序列进行功能化,与带有 FRET 受体 ATTO647N 的短寡核苷酸杂交。获得的 40nm 聚(甲基丙烯酸甲酯)基 NP 探针,封装了十八烷基罗丹明 6G 染料和四(全氟叔丁氧基)铝酸盐抗衡离子(每个 NP 约 6000 个染料),并带有 65 个受体,显示出高效的 FRET,量子产率超过 20%,并且具有 25 的信号放大(天线效应)。它通过 FRET 受体置换对靶 DNA 表现出比率响应,并能够通过荧光光谱法在溶液中(检测限为 3 pM)和在表面上(使用双色荧光显微镜)在单粒子水平上进行 DNA 检测。使用智能手机 RGB 摄像头,可以在 10 pM 目标物的真彩色和红-绿比图像中轻松检测到纳米探针的响应。因此,我们基于 FRET 的纳米颗粒生物传感器能够使用智能手机与适当的光学设备结合检测核酸靶标,为简单且廉价的即时检测分析方法开辟了道路。

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