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基于DNA适配体-量子点的弯曲杆菌磁性夹心分析方法的进一步表征及独立验证

Further characterization and independent validation of a DNA aptamer-quantum dot-based magnetic sandwich assay for Campylobacter.

作者信息

Bruno John G, Sivils Jeffrey C

机构信息

Operational Technologies Corporation, 4100 NW Loop 410, Suite 230, San Antonio, TX, 78229, USA.

出版信息

Folia Microbiol (Praha). 2017 Nov;62(6):485-490. doi: 10.1007/s12223-017-0520-0. Epub 2017 Mar 24.

Abstract

Previously reported DNA aptamers developed against surface proteins extracted from Campylobacter jejuni were further characterized by aptamer-based Western blotting and shown to bind epitopes on proteins weighing ~16 and 60 kD from reduced C. jejuni and Campylobacter coli lysates. Proteins of these approximate weights have also been identified in traditional antibody-based Western blots of Campylobacter spp. Specificity of the capture and reporter aptamers from the previous report was further validated by aptamer-based ELISA-like (ELASA) colorimetric microplate assay. Finally, the limit of detection of the previously reported plastic-adherent aptamer-magnetic bead and aptamer-quantum dot sandwich assay (PASA) was validated by an independent food safety testing laboratory to lie between 5 and 10 C. jejuni cells per milliliter in phosphate buffered saline and repeatedly frozen and thawed chicken rinsate. Such ultrasensitive and rapid (30 min) aptamer-based assays could provide alternative or additional screening tools to enhance food safety testing for Campylobacter and other foodborne pathogens.

摘要

先前报道的针对从空肠弯曲杆菌中提取的表面蛋白开发的DNA适配体,通过基于适配体的蛋白质印迹法进一步表征,并显示其与还原型空肠弯曲杆菌和大肠弯曲杆菌裂解物中重量约为16 kD和60 kD的蛋白质上的表位结合。在弯曲杆菌属的传统基于抗体的蛋白质印迹中也鉴定出了这些近似重量的蛋白质。通过基于适配体的类ELISA(ELASA)比色微孔板测定法进一步验证了先前报道的捕获适配体和报告适配体的特异性。最后,一个独立的食品安全检测实验室验证了先前报道的塑料粘附适配体-磁珠和适配体-量子点夹心测定法(PASA)的检测限,在磷酸盐缓冲盐水以及反复冻融的鸡肉冲洗液中为每毫升5至10个空肠弯曲杆菌细胞。这种超灵敏且快速(30分钟)的基于适配体的测定法可为加强弯曲杆菌和其他食源性病原体的食品安全检测提供替代或额外的筛选工具。

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