Laboratory of Biotechnology, Research Institute of Green Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan.
Laboratory of Biotechnology, Research Institute of Green Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan; Laboratory of Biotechnology, Department of Bioscience, Graduate School of Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan.
Biosens Bioelectron. 2016 Jun 15;80:483-490. doi: 10.1016/j.bios.2016.02.020. Epub 2016 Feb 9.
Conventional techniques used to diagnose influenza virus face several challenges, such as low sensitivity, slow detection, false positive results and misinterpreted data. Hence, diagnostic probes that can offer robust detection qualities, such as high sensitivity, rapid detection, elimination of false positive data, and specificity for influenza virus, are urgently needed. The near-infrared (NIR) range is an attractive spectral window due to low photon absorption by biological tissues, hence well-constructed fluorescent biosensors that emit within the NIR window can offer an improved limit of detection (LOD). Here, we demonstrate the use of a newly synthesized NIR quinternary alloyed CdZnSeTeS quantum dots (QDs) as an ultrasensitive fluorescence reporter in a conjugated molecular beacon (MB) assay to detect extremely low concentrations of influenza virus H1N1 RNA. Under optimum conditions, two different strains of influenza virus H1N1 RNA were detected based on fluorescence enhancement signal transduction. We successfully discriminated between two different strains of influenza virus H1N1 RNA based on the number of complementary nucleotide base pairs of the MB to the target RNA sequence. The merits of our bioprobe system are rapid detection, high sensitivity (detects H1N1 viral RNA down to 2 copies/mL), specificity and versatility (detects H1N1 viral RNA in human serum). For comparison, a conventional CdSe/ZnS-MB probe could not detect the extremely low concentrations of H1N1 viral RNA detected by our NIR alloyed CdZnSeTeS-MB probe. Our bioprobe detection system produced a LOD as low as ~1 copy/mL and is more sensitive than conventional molecular tests and rapid influenza detection tests (RIDTS) probes.
传统的用于诊断流感病毒的技术面临着许多挑战,例如灵敏度低、检测速度慢、假阳性结果和数据误判。因此,迫切需要能够提供稳健检测质量的诊断探针,例如高灵敏度、快速检测、消除假阳性数据以及对流感病毒的特异性。近红外(NIR)范围是一个有吸引力的光谱窗口,因为生物组织对光子的吸收较低,因此在 NIR 窗口内发射的构造良好的荧光生物传感器可以提供改进的检测限(LOD)。在这里,我们展示了一种新合成的 NIR 五元合金 CdZnSeTeS 量子点(QDs)作为共轭分子信标(MB)测定法中极其灵敏的荧光报告分子,以检测极低浓度的流感病毒 H1N1 RNA。在最佳条件下,根据荧光增强信号转导,检测了两种不同株系的流感病毒 H1N1 RNA。我们成功地根据 MB 与靶 RNA 序列的互补核苷酸碱基对的数量区分了两种不同株系的流感病毒 H1N1 RNA。我们的生物探针系统的优点是快速检测、高灵敏度(检测到 H1N1 病毒 RNA 低至 2 拷贝/mL)、特异性和多功能性(在人血清中检测到 H1N1 病毒 RNA)。相比之下,常规的 CdSe/ZnS-MB 探针无法检测到我们的 NIR 合金 CdZnSeTeS-MB 探针检测到的极低浓度的 H1N1 病毒 RNA。我们的生物探针检测系统的检测限低至约 1 拷贝/mL,比常规分子检测和快速流感检测试验(RIDTS)探针更灵敏。