首页> 外文期刊>Analytical Letters >Detection of DNA Hybridization via Fluorescence Intensity Variations of ZnSe-DNA Quantum Dot Biosensors
【24h】

Detection of DNA Hybridization via Fluorescence Intensity Variations of ZnSe-DNA Quantum Dot Biosensors

机译:ZnSe-DNA量子点生物传感器的荧光强度变化检测DNA杂交。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

ZnSe quantum dots (QDs) that were capped with 11-mercaptoundecanoic acid (MUA) and conjugated to amino-modified ssDNA molecules exhibited variations in fluorescence emission intensity upon hybridization with complementary ssDNA in solution, a phenomenon that can be exploited for rapid detection of free ssDNA sequences. Conjugation of MUA-capped ZnSe QDs to amino-modified ssDNA molecules resulted in increased fluorescence emission intensity and stability at room temperature. Increasing the length of the ssDNA, that was conjugated to the QDs, resulted in increased fluorescence emission intensity up to a length of about 50 nucleotide bases, beyond which the peak emission intensity reached a plateau. Hybridization of QD-ssDNA conjugates with complementary ssDNA, either in free form or bound to QDs from the same population, resulted in additional fluorescence emission intensity amplification. A small red shift was observed when three-dimensional QD-dsDNA-QD structures were formed. The QD-ssDNA sensors with single ssDNA molecule per QD were developed and used for rapid quantitative detection of fully or partially complementary free ssDNA sequences in aqueous solution. Partial hybridization of the QD-ssDNA sensors with short ssDNA targets resulted in smaller QD emission intensity amplification, when compared to full hybridization. A QD-ssDNA sensor containing a sequence corresponding to the hemoglobin beta gene was used to detect and discriminate between free ssDNA targets consisting of a complementary ssDNA sequence and targets containing a single-base mutation that can cause sickle-cell anemia. Such QD-based biosensors can form the basis for rapid separation-free assays that can be used to detect target biomolecules in solution.View full textDownload full textKeywordsBiosensors, DNA mutation detection, DNA sequence detection, Flourescence intensity variation, Homogeneous separation-free assays, Nanocrystal-DNA bioconjunction, Quantum dots, Zinc selenide nanocrystalsRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/00032719.2011.633190
机译:ZnSe量子点(QDs)被11-巯基癸酸(MUA)封盖并与氨基修饰的ssDNA分子缀合后,与溶液中的互补ssDNA杂交后,荧光发射强度发生变化,这种现象可用于快速检测游离态ssDNA序列。 MUA封口的ZnSe QD与氨基修饰的ssDNA分子的缀合导致室温下荧光发射强度和稳定性增加。增加与QD偶联的ssDNA的长度,导致荧光发射强度增加,直至大约50个核苷酸碱基的长度,超过此长度,峰值发射强度达到平稳状态。 QD-ssDNA缀合物与互补ssDNA的游离形式或与来自同一种群的QD的杂交,导致了额外的荧光发射强度扩增。当形成三维QD-dsDNA-QD结构时,观察到小的红移。开发了每个QD具有单个ssDNA分子的QD-ssDNA传感器,并用于快速定量检测水溶液中完全或部分互补的游离ssDNA序列。与完全杂交相比,具有短ssDNA靶标的QD-ssDNA传感器的部分杂交导致较小的QD发射强度扩增。包含与血红蛋白β基因相对应的序列的QD-ssDNA传感器用于检测和区分由互补ssDNA序列组成的游离ssDNA靶标和含有可能导致镰状细胞性贫血的单碱基突变的靶标。此类基于QD的生物传感器可以构成可用于检测溶液中目标生物分子的快速无分离测定的基础。查看全文下载全文关键词生物传感器纳米晶体-DNA生物结合体,量子点,硒化锌纳米晶体pubid:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/00032719.2011.633190

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