Low Kim-Fatt, Rijiravanich Patsamon, Singh Kirnpal Kaur Banga, Surareungchai Werasak, Yean Chan Yean
J Biomed Nanotechnol. 2015 Apr;11(4):702-10. doi: 10.1166/jbn.2015.1956.
An ultrasensitive electrochemical genosensing assay was developed for the sequence-specific detection of Vibrio cholerae DNA using magnetic beads as the biorecognition surface and gold nanoparticle-loaded latex microspheres (latex-AuNPs) as a signal-amplified hybridization tag. This biorecognition surface was prepared by immobilizing specific biotinylated capturing probes onto the streptavidin-coupled magnetic beads. Fabricating a hybridization tag capable of amplifying the electrochemical signal involved loading multiple AuNPs onto polyelectrolyte multilayer film-coated poly(styrene-co-acrylic acid) latex microspheres as carrier particles. The detection targets, single-stranded 224-bp asymmetric PCR amplicons of the V. cholerae lolB gene, were sandwich-hybridized to magnetic bead-functionalized capturing probes and fluorescein-labeled detection probes and tagged with latex-AuNPs. The subsequent electrochemical stripping analysis of chemically dissolved AuNPs loaded onto the latex microspheres allowed for the quantification of the target amplicons. The high-loading capacity of the AuNPs on the latex microspheres for sandwich-type dual-hybridization genosensing provided eminent signal amplification. The genosensing variables were optimized, and the assay specificity was demonstrated. The clinical applicability of the assay was evaluated using spiked stool specimens. The current signal responded linearly to the different V. cholerae concentrations spiked into stool specimens with a detection limit of 2 colony-forming units (CFU)/ml. The proposed latex-AuNP-based magnetogenosensing platform is promising, exhibits an effective amplification performance, and offers new opportunities for the ultrasensitive detection of other microbial pathogens.
开发了一种超灵敏电化学基因传感检测方法,用于霍乱弧菌DNA的序列特异性检测,该方法以磁珠作为生物识别表面,以负载金纳米颗粒的乳胶微球(乳胶-AuNPs)作为信号放大杂交标签。通过将特异性生物素化捕获探针固定在链霉亲和素偶联的磁珠上来制备这种生物识别表面。制备能够放大电化学信号的杂交标签包括将多个金纳米颗粒负载到聚电解质多层膜包覆的聚(苯乙烯-共-丙烯酸)乳胶微球作为载体颗粒上。检测靶标为霍乱弧菌lolB基因的单链224 bp不对称PCR扩增子,通过夹心杂交与磁珠功能化捕获探针和荧光素标记的检测探针结合,并用乳胶-AuNPs进行标记。随后对负载在乳胶微球上的化学溶解金纳米颗粒进行电化学溶出分析,从而对靶标扩增子进行定量。乳胶微球上金纳米颗粒对夹心型双杂交基因传感的高负载能力提供了显著的信号放大。对基因传感变量进行了优化,并证明了该检测方法的特异性。使用加标的粪便标本评估了该检测方法的临床适用性。电流信号对添加到粪便标本中的不同霍乱弧菌浓度呈线性响应,检测限为2个菌落形成单位(CFU)/ml。所提出的基于乳胶-AuNP的磁基因传感平台具有前景,表现出有效的放大性能,并为其他微生物病原体的超灵敏检测提供了新机会。