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一种用于细胞内端粒酶活性原位“开-关”荧光成像的新型DNA四面体-发夹探针。

A novel DNA tetrahedron-hairpin probe for in situ"off-on" fluorescence imaging of intracellular telomerase activity.

作者信息

Feng Qiu-Mei, Zhu Meng-Jiao, Zhang Ting-Ting, Xu Jing-Juan, Chen Hong-Yuan

机构信息

State Key Laboratory of Analytical Chemistry for Life Science and Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, P.R. China.

出版信息

Analyst. 2016 Apr 21;141(8):2474-80. doi: 10.1039/c6an00241b. Epub 2016 Mar 16.

Abstract

A novel three-dimensionally structured DNA probe is reported to realize in situ"off-on" imaging of intracellular telomerase activity. The probe consists of a DNA tetrahedron and a hairpin DNA on one of the vertices of the DNA tetrahedron. It is composed of four modified DNA segments: S1-Au nanoparticle (NP) inserting a telomerase strand primer (TSP) and S2-S4, three Cy5 dye modified DNA segments. Fluorescence of Cy5 at three vertices of the DNA tetrahedron is quenched by the Au NP at the other vertex due to the effective fluorescence resonance energy transfer (FRET) ("off" state). When the probe meets telomerase, the hairpin structure changes to rod-like through complementary hybridization with the telomerase-triggered stem elongation product, resulting in a large distance between the Au NP and Cy5 and the recovery of Cy5 fluorescence ("on" state). The molar ratio of 3 : 1 between the reporter (Cy5) and the target related TSP makes the probe show high sensitivity and recovery efficiency of Cy5 in the presence of telomerase extracted from HeLa cells. Given the functional and compact nanostructure, the mechanically stable and noncytotoxic nature of the DNA tetrahedron, this FRET-based probe provides more opportunities for biosensing, molecular imaging and drug delivery.

摘要

据报道,一种新型的三维结构DNA探针可实现细胞内端粒酶活性的原位“开-关”成像。该探针由一个DNA四面体和位于DNA四面体一个顶点上的发夹DNA组成。它由四个修饰的DNA片段组成:插入端粒酶链引物(TSP)的S1-金纳米颗粒(NP)以及三个Cy5染料修饰的DNA片段S2-S4。由于有效的荧光共振能量转移(FRET)(“关”状态),DNA四面体三个顶点处的Cy5荧光被另一个顶点处的金纳米颗粒淬灭。当探针与端粒酶相遇时,发夹结构通过与端粒酶触发的茎伸长产物的互补杂交而变为棒状,导致金纳米颗粒与Cy5之间的距离增大,Cy5荧光恢复("开"状态)。报告基团(Cy5)与靶标相关TSP之间3:1的摩尔比使得该探针在存在从HeLa细胞中提取的端粒酶时显示出高灵敏度和Cy5的恢复效率。鉴于DNA四面体的功能性和紧凑的纳米结构、机械稳定性和无细胞毒性的性质,这种基于FRET的探针为生物传感、分子成像和药物递送提供了更多机会。

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