首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Double G-quadruplexes in a copper nanoparticle based fluorescent probe for determination of HIV genes
【24h】

Double G-quadruplexes in a copper nanoparticle based fluorescent probe for determination of HIV genes

机译:基于铜纳米粒子的荧光探针中的双G-四翻探针,用于测定HIV基因

获取原文
获取原文并翻译 | 示例
           

摘要

A DNA-templated copper nanoparticle (CuNP) probe has been developed for the determination of the human immunodeficiency virus oligonucleotide (HIV-DNA). The function of the probe relies on affinity binding-induced DNA hybridization associated with the use of double G-quadruplexes. Double-stranded DNA(dsDNA) with poly(AT-TA) bases was used as a template for synthesis of dsDNA-CuNPs. These have weak fluorescence. In the next step, two G-rich sequences that are linked to both sides of the ds-DNA are locked by HIV complementary DNA (cDNA). If HIV-DNA is introduced, it will hybridize with cDNA, thereby transforming the two G-rich sequences into G-quadruplexes. This enhances the fluorescence of the adjacent dsDNA-CuNPs. Fluorescence increases linearly in the 1 to 200 and 250-1000nM HIV-DNA concentration range, and the detection limit is 13 pM. This enzyme-free fluorometric assay is time-saving, easily operated, and therefore has large potential in biosensing because it may be extended to various other DNA targets.
机译:已经开发了DNA模板铜纳米粒子(CUNP)探针用于测定人免疫缺陷病毒寡核苷酸(HIV-DNA)。探针的功能依赖于与使用双g-四翻来的亲和结合诱导的DNA杂交。具有聚(AT-TA)碱基的双链DNA(DSDNA)用作合成DSDNA-CUNP的模板。这些具有弱荧光。在下一步中,通过HIV互补DNA(cDNA)锁定与DS-DNA的两侧连接的富含G的富含含量。如果引入HIV-DNA,则将其与cDNA杂交,从而将两个G的序列转化为G-四翻转。这增强了相邻的DSDNA-CUNP的荧光。荧光在1至200和250-1000nm的HIV-DNA浓度范围内线性增加,并且检测极限是下午13点。这种无酶荧光测定法是省气的,容易操作,因此在生物沉积中具有很大的电位,因为它可以扩展到各种其他DNA靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号