Suppr超能文献

硫化镉纳米颗粒作为寡核苷酸标记物在电化学检测NOS终止子基因序列中的应用。

Application of cadmium sulfide nanoparticles as oligonucleotide labels for the electrochemical detection of NOS terminator gene sequences.

作者信息

Sun Wei, Zhong Jianghua, Zhang Bo, Jiao Kui

机构信息

College of Chemistry and Molecular Engineering, Key Laboratory of Eco-Chemical Engineering of Ministry of Education, Qingdao University of Science and Technology, Qingdao, 266042, China.

出版信息

Anal Bioanal Chem. 2007 Dec;389(7-8):2179-84. doi: 10.1007/s00216-007-1661-9. Epub 2007 Oct 16.

Abstract

A mercaptoacetic acid (MAA)-modified cadmium sulfide (CdS) nanoparticle was synthesized in aqueous solution and used as an oligonucleotide label for the electrochemical detection of nopaline synthase (NOS) terminator gene sequence. The carboxyl groups on the surface of the CdS nanoparticle can be easily covalently linked with NH2-modified NOS oligonucleotide probe sequences. The target ssDNA sequence was fixed onto the electrode surface by covalently linking to a mercaptoethanol self-assembled gold electrode, and the DNA hybridization of target ssDNA with probe ssDNA was accomplished on the electrode surface. The CdS nanoparticles anchored on the hybrids were dissolved in the solution by the oxidation with HNO3 and further detected by a sensitive differential pulse anodic stripping voltammetric method. The detection results can be used for monitoring the hybridization, and the NOS target sequence was satisfactorily detected in the approximate range from 8.0 x 10(-12) to 4.0 x 10(-9) mol L(-1) with a detection limit of 2.75 x 10(-12) mol L(-1) (3sigma). The established method extended the nanoparticle-labeled electrochemical DNA analysis to genetically modified organisms (GMOs) specific sequence samples with higher sensitivity and selectivity.

摘要

在水溶液中合成了巯基乙酸(MAA)修饰的硫化镉(CdS)纳米颗粒,并将其用作寡核苷酸标记物,用于电化学检测胭脂碱合成酶(NOS)终止子基因序列。CdS纳米颗粒表面的羧基可轻松与氨基修饰的NOS寡核苷酸探针序列共价连接。通过与巯基乙醇自组装金电极共价连接,将目标单链DNA序列固定在电极表面,并在电极表面完成目标单链DNA与探针单链DNA的DNA杂交。通过用HNO3氧化,将锚定在杂交体上的CdS纳米颗粒溶解在溶液中,并通过灵敏的差分脉冲阳极溶出伏安法进一步检测。检测结果可用于监测杂交情况,在大约8.0×10^(-12)至4.0×10^(-9) mol L^(-1)的范围内令人满意地检测到了NOS目标序列,检测限为2.75×10^(-12) mol L^(-1)(3σ)。所建立的方法将纳米颗粒标记的电化学DNA分析扩展到了具有更高灵敏度和选择性的转基因生物(GMO)特定序列样品。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验