An ultrasensitive SiO2-encapsulated alloyed CdZnSeS quantum dot-molecular beacon nanobiosensor for norovirus

被引:43
作者
Adegoke, Oluwasesan [1 ]
Seo, Min-Woong [2 ]
Kato, Tatsuya [1 ,3 ]
Kawahito, Shoji [2 ]
Park, Enoch Y. [1 ,3 ]
机构
[1] Shizuoka Univ, Res Inst Green Sci & Technol, Biotechnol Lab, Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
[2] Shizuoka Univ, Elect Res Inst, Imaging Devices Lab, Naka Ku, Johoku 3-5-1, Hamamatsu, Shizuoka 4328011, Japan
[3] Shizuoka Univ, Grad Sch Sci & Technol, Biotechnol Lab, Dept Biosci,Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
基金
日本学术振兴会;
关键词
Molecular beacon; Quantum dots; Alloy; Norovirus virus; RNA; Bioprobe; REVERSE TRANSCRIPTION-PCR; SEMICONDUCTOR NANOCRYSTALS; ASSAY; SINGLE; VIRUS;
D O I
10.1016/j.bios.2016.06.027
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Ultrasensitive, rapid and selective diagnostic probes are urgently needed to overcome the limitations of traditional probes for norovirus (NV). Here, we report the detection of NV genogroup II via nucleic acid hybridization technology using a quantum dot (QD)-conjugated molecular beacon (MB) probe. To boost the sensitivity of the MB assay system, an ultrasensitive QD fluorophore with unique optical properties was synthesized, characterized and exploited as a fluorescence signal generator. Alloyed thioglycolic (TGA)-capped CdZnSeS QDs with a high photoluminescence (PL) quantum yield (QY) value of 92% were synthesized, and a modified silanization method was employed to encapsulate the thiol-capped QDs in a silica layer. The resulting highly luminescent alloyed SiO2-coated CdZnSeS QDs had a remarkable PL QY value of 98%. Transmission electron microscopy and dynamic light scattering confirmed the monodispersity of the alloyed nanocrystals, and zeta potential analysis confirmed their colloidal stability. Powder X-ray diffraction and PL lifetime measurements confirmed the surface modification of the QDs. The alloyed TGA-capped and SiO2-coated CdZnSeS QD-conjugated MB bioprobes detected extremely low concentrations of NV RNA. Ultrasensitive detection of low concentrations of NV RNA with a limit of detection (LOD) of 8.2 copies/mL in human serum and a LOD of 9.3 copies/mL in buffer was achieved using the SiO2-coated CdZnSeS QD-MB probes, an increase in sensitivity of 3-fold compared with the detection limit for NV RNA using TGA-capped CdZnSeS QD-MBs. The additional merits of our detection system are rapidity, specificity and improved sensitivity over conventional molecular test probes. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:135 / 142
页数:8
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