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血清及血清 - 十二烷基硫酸钠中DNA与RNA杂交的动力学

Kinetics of DNA and RNA Hybridization in Serum and Serum-SDS.

作者信息

Graugnard Elton, Cox Amber, Lee Jeunghoon, Jorcyk Cheryl, Yurke Bernard, Hughes William L

机构信息

Department of Materials Science & Engineering, Boise State University, Boise, ID 83725 USA.

出版信息

IEEE Trans Nanotechnol. 2010 Sep 1;9(5):603-609. doi: 10.1109/TNANO.2010.2053380.

DOI:10.1109/TNANO.2010.2053380
PMID:20967137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2957020/
Abstract

Cancer is recognized as a serious health challenge both in the United States and throughout the world. While early detection and diagnosis of cancer leads to decreased mortality rates, current screening methods require significant time and costly equipment. Recently, increased levels of certain micro-ribonucleic acids (miRNAs) in the blood have been linked to the presence of cancer. While blood-based biomarkers have been used for years in cancer detection, studies analyzing trace amounts of miRNAs in blood and serum samples are just beginning. Recent developments in deoxyribonucleic acid (DNA) nanotechnology and DNA computing have shown that it is possible to construct nucleic-acid-based chemical networks that accept miRNAs as inputs, perform Boolean logic functions on those inputs, and generate as an output a large number of DNA strands that can readily be detected. Since miRNAs occur in blood in low abundance, these networks would allow for amplification without using polymerase chain reaction. In this study, we report initial progress in the development of a DNA-based cross-catalytic network engineered to amplify specific cancer-related miRNAs. Subcomponents of the DNA network were tested individually, and their operation in serum, as well as a mixture of serum with sodium dodecyl sulfate, is demonstrated. Preliminary simulations of the full cross-catalytic network indicate successful operation.

摘要

癌症在美国乃至全世界都是一项严峻的健康挑战。尽管癌症的早期检测和诊断能降低死亡率,但当前的筛查方法需要耗费大量时间且设备成本高昂。最近,血液中某些微小核糖核酸(miRNA)水平的升高与癌症的存在有关。虽然基于血液的生物标志物多年来一直用于癌症检测,但分析血液和血清样本中痕量miRNA的研究才刚刚起步。脱氧核糖核酸(DNA)纳米技术和DNA计算的最新进展表明,构建以核酸为基础的化学网络是可行的,该网络可以将miRNA作为输入,对这些输入执行布尔逻辑功能,并生成大量易于检测的DNA链作为输出。由于miRNA在血液中的丰度较低,这些网络无需使用聚合酶链反应就能实现扩增。在本研究中,我们报告了一种基于DNA的交叉催化网络的初步开发进展,该网络旨在扩增特定的癌症相关miRNA。对DNA网络的子组件进行了单独测试,并展示了它们在血清以及血清与十二烷基硫酸钠混合物中的运行情况。对完整交叉催化网络的初步模拟表明其运行成功。

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