用于实时DNA突变检测的微加热器阵列装置的研制与表征

SPIE MOEMS-MEMS Pub Date : 2008-02-07 DOI:10.1117/12.767286
Layne D. Williams, M. Okandan, A. Chagovetz, S. Blair
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引用次数: 1

摘要

DNA分析,特别是单核苷酸多态性(SNP)检测,在快速诊断和疾病检测中变得越来越重要。温度通常被控制,以帮助加快反应速率和执行熔融杂化寡核苷酸。对于给定的探针寡核苷酸,野生型和SNP序列之间的熔融温度Tm的差异表明了反应的特异性。我们在溶液和固体底物上鉴定了来自囊性纤维化相关的已知突变的三个序列的Tm。利用Tm的差异,设计了一种微加热器阵列装置,可以对多达18个特定杂交事件进行单独的温度控制。该装置是在桑迪亚国家实验室使用表面微加工技术制造的。利用桑迪亚的红外摄像机对微加热器进行了表征,并显示出以最小的热串扰进行单独的温度控制。描述了该装置作为实时DNA检测平台的发展,包括表面化学和相关的微流体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and characterization of a microheater array device for real-time DNA mutation detection
DNA analysis, specifically single nucleotide polymorphism (SNP) detection, is becoming increasingly important in rapid diagnostics and disease detection. Temperature is often controlled to help speed reaction rates and perform melting of hybridized oligonucleotides. The difference in melting temperatures, Tm, between wild-type and SNP sequences, respectively, to a given probe oligonucleotide, is indicative of the specificity of the reaction. We have characterized Tm's in solution and on a solid substrate of three sequences from known mutations associated with Cystic Fibrosis. Taking advantage of Tm differences, a microheater array device was designed to enable individual temperature control of up to 18 specific hybridization events. The device was fabricated at Sandia National Laboratories using surface micromachining techniques. The microheaters have been characterized using an IR camera at Sandia and show individual temperature control with minimal thermal cross talk. Development of the device as a real-time DNA detection platform, including surface chemistry and associated microfluidics, is described.
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