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SERS-based immunoassay of tumor marker VEGF using DNA aptamers and silica-encapsulated hollow gold nanospheres

机译:使用DNA适体和硅胶包裹的空心金纳米球进行基于SERS的肿瘤标志物VEGF免疫分析

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摘要

A novel SERS-based sandwich immunoassay using DNA aptamers, silica-encapsulated hollow gold nanospheres (SEHGNs) and a gold-patterned microarray was developed for sensitive detection of VEGF (vascular endothelial growth factor) angiogenesis protein markers. Here, a DNA aptamer conjugated to SEHGN was used as a highly reproducible SERS-encoding nanoprobe, and a hybrid microarray including hydrophilic gold wells and other hydrophobic areas was used as a SERS substrate. Target specific DNA aptamers that fold into a G-quadruplex structure were used as a target recognition unit instead of VEGF antibodies. The detection sensitivity was increased by 2 or 3 orders of magnitude over the conventional ELISA method. In particular, the dynamic concentration range was 3 or 4 orders of magnitude greater than that of conventional ELISA. The results demonstrate that this sensing strategy using DNA aptamers is a powerful platform for the design of novel immune-sensors with high performance. In particular, SERS-based detection using SEHGNs provides great promise for highly sensitive biomarker sensing with unprecedented advantages.
机译:一种新型的基于SERS的夹心免疫测定法,利用DNA适体,硅胶包裹的空心金纳米球(SEHGNs)和金制微阵列技术开发,用于检测VEGF(血管内皮生长因子)血管生成蛋白标记。在这里,与SEHGN缀合的DNA适体被用作高度可复制的编码SERS的纳米探针,而包含亲水金孔和其他疏水区域的杂交微阵列被用作SERS底物。折叠成G-四链体结构的靶标特异性DNA适体代替VEGF抗体用作靶标识别单元。与传统的ELISA方法相比,检测灵敏度提高了2或3个数量级。特别地,动态浓度范围比常规ELISA大3或4个数量级。结果表明,这种使用DNA适体的传感策略是设计高性能新型免疫传感器的强大平台。特别是,使用SEHGNs的基于SERS的检测为具有高度优势的高灵敏度生物标志物传感提供了广阔前景。

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