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基于适体的生物芯片用于 SPR 成像法无标记检测植物病毒外壳蛋白。

Aptamer-based biochips for label-free detection of plant virus coat proteins by SPR imaging.

机构信息

Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, Szt. Gellért tér 4, H-1111 Budapest, Hungary.

出版信息

Analyst. 2010 May;135(5):918-26. doi: 10.1039/b922829b. Epub 2010 Feb 11.

Abstract

Specific detection of virus strains by affinity-based bioassays is often limited by the availability of ligands able to differentiate among close homologues of virus coat proteins. As viruses are prone to mutation, the ligand generation should, in addition, be fast enough to allow rapid identification of new varieties. These two criteria are difficult to be fulfilled by antibodies; however, they open up opportunities for aptamer-based detection. Here we report on the feasibility of selectively detecting the apple stem pitting virus (ASPV) coat proteins (PSA-H, MT32) using original DNA aptamers. Surface plasmon resonance (SPR) imaging was used together with aptamer-modified sensor chips to optimize the aptamer immobilization for highest sensitivity and to characterize the aptamer-virus coat protein binding. Different parameters affecting this binding, such as the aptamer flanking, surface coverage, and type of spacer molecules, were identified and their influence was determined. A direct label-free method is proposed for assessing the ASPV based on the detection of the respective virus coat proteins in plant extracts.

摘要

基于亲和力的生物测定法对病毒株的特异性检测通常受到能够区分病毒衣壳蛋白近亲的配体的可用性的限制。由于病毒容易发生突变,配体的产生还应该足够快,以允许快速识别新变种。这两个标准很难通过抗体来满足;然而,它们为基于适配体的检测开辟了机会。在这里,我们报告了使用原始 DNA 适体选择性检测苹果茎痘病毒(ASPV)衣壳蛋白(PSA-H、MT32)的可行性。表面等离子体共振(SPR)成像与适体修饰的传感器芯片一起用于优化适体固定化以获得最高灵敏度,并表征适体-病毒衣壳蛋白的结合。确定了影响这种结合的不同参数,例如适体侧翼、表面覆盖率和间隔分子的类型,并确定了它们的影响。提出了一种直接的无标记方法,用于基于在植物提取物中检测各自的病毒衣壳蛋白来评估 ASPV。

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