Electronics and Photonics Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan.
PLoS One. 2013 Jul 11;8(7):e69121. doi: 10.1371/journal.pone.0069121. Print 2013.
Gold nanoparticles were conjugated to an antibody (immuno-AuNP) against A/Udorn/307/1972 (H3N2) influenza virus to detect viruses on a sensing plate designed for an evanescent field-coupled waveguide-mode sensor. Experiments were conducted using human influenza A/H3N2 strains, and immuno-AuNP could detect 8×10(5) PFU/ml (40 pg/µl) intact A/Udorn/307/1972 and 120 pg/µl A/Brisbane/10/2007. Furthermore, increased signal magnitude was achieved in the presence of non-ionic detergent, as the virtual detection level was increased to 8×10(4) PFU/ml A/Udorn/307/1972. Immuno-AuNPs were then complexed with viruses to permit direct observation, and they formed a ring of confined nanodots on the membrane of both intact and detergent-treated viruses as directly visualized by scanning electron microscopy. With this complex the detection limit was improved further to 8×10(3) PFU/ml on anti-rabbit IgG immobilized sensing plate. These strategies introduce methods for observing trapped intact viruses on the sensing plates generated for optical systems.
金纳米粒子被连接到针对 A/Udorn/307/1972(H3N2)流感病毒的抗体(免疫 AuNP)上,以在为瞬逝场耦合波导模式传感器设计的传感板上检测病毒。实验使用人源甲型流感 A/H3N2 株进行,免疫 AuNP 可检测到 8×10(5)PFU/ml(40 pg/µl)完整的 A/Udorn/307/1972 和 120 pg/µl A/Brisbane/10/2007。此外,在存在非离子型洗涤剂的情况下,信号幅度增加,因为虚拟检测水平提高到 8×10(4)PFU/ml A/Udorn/307/1972。然后将免疫 AuNP 与病毒复合,允许直接观察,并且它们在完整和用洗涤剂处理的病毒的膜上形成了一个受限纳米点环,这可以通过扫描电子显微镜直接可视化。通过这种复合物,在固定有抗兔 IgG 的传感板上,检测限进一步提高到 8×10(3)PFU/ml。这些策略为在光学系统产生的传感板上观察捕获的完整病毒引入了方法。