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引用次数: 0
摘要
基于荧光的灵敏传感器一直被视为创新的分析工具,可用于检测和定量许多领域(包括医学和治疗学)中的分析物。传统的分子信标灵敏传感器设计使用 DNA 合体作为生物传感器的识别元件,利用 DNA 合体的目标诱导结构转换来产生可测量的荧光信号。然而,并非所有的 DNA 合体都会发生足够的目标特异性构象变化,从而产生显著的荧光测量结果。在此,我们建议使用互补的 "反义 "链,在与目标结合时通过链位移进行荧光测量。利用已发表的针对 SARS-CoV-2 受体结合结构域的目标特异性 DNA 类似物,我们设计了一种链霉亲和素-类似物珠复合物,用于目标检测的荧光位移测定。所开发的检测方法的线性范围为 50 至 800 纳摩尔(nM),检测限为 67.5 nM,定量限为 204.5 nM。通过对合适的靶标特异性 DNA 类似物及其互补反义链进行调整和功能化,该方法为检测和定量任何感兴趣的靶标提供了一种 "适用于目的 "的检测模型。
Enhancing Target Detection: A Fluorescence-Based Streptavidin-Bead Displacement Assay.
Fluorescence-based aptasensors have been regarded as innovative analytical tools for the detection and quantification of analytes in many fields, including medicine and therapeutics. Using DNA aptamers as the biosensor recognition component, conventional molecular beacon aptasensor designs utilise target-induced structural switches of the DNA aptamers to generate a measurable fluorescent signal. However, not all DNA aptamers undergo sufficient target-specific conformational changes for significant fluorescence measurements. Here, the use of complementary 'antisense' strands is proposed to enable fluorescence measurement through strand displacement upon target binding. Using a published target-specific DNA aptamer against the receptor binding domain of SARS-CoV-2, we designed a streptavidin-aptamer bead complex as a fluorescence displacement assay for target detection. The developed assay demonstrates a linear range from 50 to 800 nanomolar (nM) with a limit of detection calculated at 67.5 nM and a limit of quantification calculated at 204.5 nM. This provides a 'fit-for-purpose' model assay for the detection and quantification of any target of interest by adapting and functionalising a suitable target-specific DNA aptamer and its complementary antisense strand.
Biosensors-BaselBiochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
6.60
自引率
14.80%
发文量
983
审稿时长
11 weeks
期刊介绍:
Biosensors (ISSN 2079-6374) provides an advanced forum for studies related to the science and technology of biosensors and biosensing. It publishes original research papers, comprehensive reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.