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电化学生物传感器在检测有毒藻类中的应用进展。

Advances in the Detection of Toxic Algae Using Electrochemical Biosensors.

机构信息

Marine Biological Association of the UK, The Citadel, Plymouth PL1 2PB, UK.

Department of Analytical Chemistry, Universidad Complutense de Madrid, E-28040 Madrid, Spain.

出版信息

Biosensors (Basel). 2020 Dec 16;10(12):207. doi: 10.3390/bios10120207.

Abstract

Harmful algal blooms (HABs) are more frequent as climate changes and tropical toxic species move northward, especially along the Iberian Peninsula, a rich aquaculture area. Monitoring programs, detecting the presence of toxic algae before they bloom, are of paramount importance to protect ecosystems, aquaculture, human health and local economies. Rapid, reliable species identification methods using molecular barcodes coupled to biosensor detection tools have received increasing attention as an alternative to the legally required but impractical microscopic counting-based techniques. Our electrochemical detection system has improved, moving from conventional sandwich hybridization protocols using different redox mediators and signal probes with different labels to a novel strategy involving the recognition of RNA heteroduplexes by antibodies further labelled with bacterial antibody binding proteins conjugated with multiple enzyme molecules. Each change has increased sensitivity. A 150-fold signal increase has been produced with our newest protocol using magnetic microbeads (MBs) and amperometric detection at screen-printed carbon electrodes (SPCEs) to detect the target RNA of toxic species. We can detect as few as 10 cells L for some species by using a fast (2 h), simple (PCR-free) and cheap methodology (2 EUR/determination) that will allow this methodology to be integrated into easy-to-use portable systems.

摘要

有害藻类水华 (HABs) 随着气候变化和热带有毒物种向北迁移而更加频繁,尤其是在伊比利亚半岛这个水产养殖丰富的地区。监测计划对于保护生态系统、水产养殖、人类健康和当地经济至关重要,该计划旨在在藻类大量繁殖之前检测有毒藻类的存在。使用分子条码与生物传感器检测工具相结合的快速、可靠的物种鉴定方法,已经越来越受到关注,因为这些方法是替代法定的但不切实际的基于显微镜计数的技术的替代方法。我们的电化学检测系统已经得到了改进,从使用不同的氧化还原介体和带有不同标签的信号探针的传统三明治杂交方案,发展到一种新的策略,即通过与多个酶分子结合的细菌抗体结合蛋白进一步标记的抗体识别 RNA 异源双链体。每个变化都提高了灵敏度。我们使用最新的方案,在磁性微珠 (MBs) 和丝网印刷碳电极 (SPCE) 上进行安培检测,检测到了目标 RNA ,从而使信号增加了 150 倍。对于某些物种,我们可以检测到低至 10 个细胞/L 的水平,因为我们的方法快速(2 小时)、简单(无 PCR)且便宜(2 欧元/测定),这将使这种方法能够集成到易于使用的便携式系统中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d064/7765624/b561075d72db/biosensors-10-00207-g001.jpg

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