Foshan Green Intelligent Manufacturing Research Institute of Xiangtan University, Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan, 411105, China.
Mikrochim Acta. 2021 Jan 27;188(2):55. doi: 10.1007/s00604-020-04680-2.
A sensitive ratiometric fluorescence probe based on hybridization chain reaction (HCR) was constructed for sensitive detection of miRNA-21 by using G-triplex and silver nanocluster pairs (AgNC pairs) as an enzyme-free and label-free signal output group. miRNA-21 was used as the primer for the hybridization chain reaction of molecular beacon 1 (MB1) containing the locked G-triplex sequence and molecular beacon 2 (MB2) with intact AgNC pairs at the 5' and 3' end activation. The double-stranded product was obtained along with the opening of the G-triplex and the separation of the AgNC pairs. A detection limit of 67 pM and a linear detection range of 0.1-300 nM were obtained for miRNA-21 determination. The proposed strategy enabled the monitoring of miRNA-21 levels in at least three cell lines, indicating that it provided new ideas for detecting miRNA in real samples. MB1 and MB2 contained the locked G-triplex sequence and silver nanocluster pairs (AgNC pairs), respectively. In the presence of target, the hybridization chain reaction (HCR) between MB1 and MB2 was initiated. At the same time, the locked G-triplex was released and combined to the dye thioflavin T (THT) to increase fluorescence, while the separation of the AgNC pairs caused the fluorescence to decrease. The double-stranded (ds) DNA product was generated to form a ratiometric signal to be detected.
基于杂交链式反应(HCR)构建了一种灵敏的荧光比率探针,通过使用 G-三链体和银纳米簇对(AgNC 对)作为无酶和无标记信号输出基团,用于灵敏检测 miRNA-21。miRNA-21 用作分子信标 1(MB1)的引物,该分子信标含有锁定的 G-三链体序列和分子信标 2(MB2),在 5'和 3'端激活时带有完整的 AgNC 对。双链产物的形成伴随着 G-三链体的打开和 AgNC 对的分离。获得了用于 miRNA-21 测定的 67 pM 的检测限和 0.1-300 nM 的线性检测范围。该提出的策略能够监测至少三种细胞系中的 miRNA-21 水平,表明它为检测真实样本中的 miRNA 提供了新的思路。MB1 和 MB2 分别含有锁定的 G-三链体序列和银纳米簇对(AgNC 对)。在存在靶标的情况下,MB1 和 MB2 之间的杂交链式反应(HCR)被启动。同时,释放锁定的 G-三链体并与染料噻唑橙 T(THT)结合以增加荧光,而 AgNC 对的分离导致荧光降低。双链(ds)DNA 产物的生成形成了可检测的比率信号。