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用于体内超灵敏定量检测微小RNA的比率型荧光共振能量转移编码分层ZrMOF@Au簇

Ratiometric FRET Encoded Hierarchical ZrMOF @ Au Cluster for Ultrasensitive Quantifying MicroRNA In Vivo.

作者信息

Liang Zichen, Hao Changlong, Chen Chen, Ma Wei, Sun Maozhong, Xu Liguang, Xu Chuanlai, Kuang Hua

机构信息

International Joint Research Laboratory for Biointerface and Biodetection, Jiangnan University, Wuxi, Jiangsu, 214122, China.

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, China.

出版信息

Adv Mater. 2022 Jan;34(1):e2107449. doi: 10.1002/adma.202107449. Epub 2021 Oct 23.

Abstract

Here, Zirconium metal-organic frameworks @ gold (ZrMOF @ Au) cluster architectures have been fabricated and then functionalized with two fluorescent dyes (Quasar [QS] and Cyanine5.5 [Cy5.5]) through deoxyribonucleic acid hybridization, to form a fluorescence resonance energy transfer (FRET) encoded ZrMOF  @  Au-QS/Cy5.5 complex. In the presence of the target intracellular microRNA (miR)-21, the fluorescence of Cy5.5 at 705 nm (F ) decreases and the fluorescence of QS at 665 nm (F ) increases when Cy5.5 is released from the surface of ZrMOF  @  Au-QS/Cy5.5. The change in the fluorescence ratio (F /F ) shows an outstanding linear range of 0.006-67.9 amol/ng , and the limit of detection is 4.51 zmol/ng in living cells. The high ratio loading of nucleic acid on surface of ZrMOF @ Au cluster and two fluorescence encoded signal enables better sensitivity and reliability. Zeptomolar sensitivity and good linearity against target affords distinct imaging-based monitoring of the cancer marker miR-21 both in living cells and in vivo. At the same time, the architecture displays remarkable photothermal conversion efficiency (53.7%) and gives rise to outstanding therapy ability in vivo. This strategy offers new avenues for the intelligent quantification of miRNAs for simultaneous diagnoses and treatments of early-stage cancers.

摘要

在此,已制备出锆基金属有机框架@金(ZrMOF@Au)簇结构,然后通过脱氧核糖核酸杂交用两种荧光染料(类喹吖因[QS]和花青素5.5[Cy5.5])进行功能化,以形成荧光共振能量转移(FRET)编码的ZrMOF@Au-QS/Cy5.5复合物。在靶细胞内微小RNA(miR)-21存在的情况下,当Cy5.5从ZrMOF@Au-QS/Cy5.5表面释放时,705nm处Cy5.5的荧光(F)降低,665nm处QS的荧光(F)增加。荧光比率(F/F)的变化显示出0.006 - 67.9 amol/ng的出色线性范围,活细胞中的检测限为4.51 zmol/ng。ZrMOF@Au簇表面核酸的高比率负载和两个荧光编码信号实现了更好的灵敏度和可靠性。zeptomolar灵敏度和对靶标的良好线性使得能够在活细胞和体内对癌症标志物miR-21进行基于成像的独特监测。同时,该结构显示出显著的光热转换效率(53.7%),并在体内产生出色的治疗能力。这种策略为智能定量检测miRNAs以同时诊断和治疗早期癌症提供了新途径。

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