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利用对G-四链体环部的构型调节进行传感器的设计

段娜娜 王娜 杨薇 孔德明

分析化学Issue(10):1414-1420,7.
分析化学Issue(10):1414-1420,7.DOI:10.11895/j.issn.0253-3820.140338

利用对G-四链体环部的构型调节进行传感器的设计

Sensor Design Based on Structure Adjustment in Loops of G-quadruplex

段娜娜 1王娜 1杨薇 1孔德明1

作者信息

  • 1. 南开大学分析科学研究中心,南开大学化学学院,天津300071
  • 折叠

摘要

Abstract

The effects of linking loop structure between guanine ( G) repeats on G-quadruplex formation were investigated. The results show that the unfavorable effects of long linking loops on G-quadruplex formation can be overcome by introducing double-stranded structures in linking loop regions. This finding provides a new way for sensor design. The activity of G-quadruplex DNAzyme can be tuned by utilizing target-mediated formation of double-stranded structures in loops. As an example, T-T mismatches are introduced in loops to destroy double-stranded structures. The stabilization of Hg2+ to T-T mismatches promotes the reformation of double-stranded structures. Correspondingly, the oligonucleotide folds into G-quadruplex, which binds with hemin to form peroxidase-like G-quadruplex DNAzyme. Hg2+ sensor is designed based on this principle. Using this method, Hg2+ quantitation is achieved in the concentration range of 10-700 nmol/L, with a detection limit of 8. 7 nmol/L. Cysteine will compete with T bases to bind with Hg2+, releasing Hg2+from T-Hg2+-T base pairs. Thus cysteine can also be quantified with this system in the concentration range of 20-700 nmol/L, with a detection limit of 14 nmol/L.

关键词

G-四链体/DNA酶/传感器/汞离子/半胱氨酸

Key words

G-quadruplex/DNAzyme/Sensor/Mercurry(Ⅱ)/Cysteine

引用本文复制引用

段娜娜,王娜,杨薇,孔德明..利用对G-四链体环部的构型调节进行传感器的设计[J].分析化学,2014,(10):1414-1420,7.

基金项目

本文系天津市应用基础与前沿科技研究计划(No.12JCYBJC13300)资助项目 (No.12JCYBJC13300)

分析化学

OA北大核心CSCDCSTPCDSCI

0253-3820

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