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Detection of DNA alterations using gold nanoparticles exploiting the LSP phenomenon

机译:利用金纳米粒子利用LSP现象检测DNA改变

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In this paper we propose the theoretical possibility to use plasmonic nanoparticles to investigate alternative gene splicing. Nanoparticle flows are transmitted by a nanomachine, and diffuse in a biological environment, till reaching a receiver. The detection process of DNA alterations is accomplished when nanoparticles are captured at the receiver, through ligand-receptor bindings. A sensing platform, consisting of a silica substraste with an array of thin gold patches, is used for the immobilization of DNA capture sequence. The colloidal particles are functionalized with specific splice junctions of gene sequences (particularly, we considered the breast cancer susceptibility gene 1), to reveal alterations that could be associated to an early disease condition. A sandwich structure occurs only if the mutation (i.e., a target sequence) is present. To test this scheme, the electromagnetic analysis of the sensing platform is derived through full-wave numerical simulations. The Extinction-Cross Section is evaluated, in the case of synchronous and asynchronous nanoparticles detection.
机译:在本文中,我们提出了使用等离激元纳米粒子研究替代基因剪接的理论可能性。纳米粒子流由纳米机器传输,并在生物环境中扩散,直到到达接收器。当通过配体-受体结合将纳米颗粒捕获在受体上时,就完成了DNA改变的检测过程。由二氧化硅基质和一系列薄金片组成的传感平台用于固定DNA捕获序列。胶体颗粒通过基因序列的特定剪接连接功能化(特别是我们认为是乳腺癌易感基因1),以揭示可能与早期疾病状况相关的改变。仅当存在突变(即靶序列)时,才发生夹心结构。为了测试该方案,通过全波数值模拟推导了感测平台的电磁分析。在同步和异步纳米粒子检测的情况下,对消光横截面进行评估。

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