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An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells

机译:一种基于适体的适体荧光探针用于检测HepG2细胞

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摘要

It is significant to develop a probe with sensitivity and specificity for the detection of cancer cells. The present study aimed to develop an ‘activatable’ aptamer-based fluorescence probe (AAFP) to detect cancer cells and frozen cancer tissue. This AAFP consisted of two fragments: aptamer TLS11a that targets HepG2 cells, and two short extending complementary DNA sequences with a 5′- and 3′-terminus that make the aptamer in hairpin structure a capable quencher to fluorophore. The ability of the AAFP to bind specifically to cancer cells was assessed using flow cytometry, fluorescence spectroscopy and fluorescence microscopy. Its ability to bind to frozen cancer tissue was assessed using fluorescence microscopy. As a result, in the absence of cancer cells, AAFP showed minimal fluorescence, reflecting auto-quenching. In the presence of cancer cells, however, AAFP showed a strong fluorescent signal. Therefore, this AAFP may be a promising tool for sensitive and specific detection of cancer.
机译:开发对癌细胞检测具有敏感性和特异性的探针具有重要意义。本研究旨在开发一种基于“适体”的适体荧光探针(AAFP),以检测癌细胞和冷冻的癌组织。该AAFP由两个片段组成:靶向HepG2细胞的适体TLS11a,以及两个带有5'-和3'-末端的短延伸互补DNA序列,使发夹结构中的适体成为荧光团的有效猝灭剂。使用流式细胞仪,荧光光谱法和荧光显微术评估AAFP与癌细胞特异性结合的能力。使用荧光显微镜评估其与冷冻癌组织结合的能力。结果,在没有癌细胞的情况下,AAFP显示出最小的荧光,反映了自动猝灭。但是,在癌细胞存在下,AAFP显示出很强的荧光信号。因此,该AAFP可能是用于灵敏和特异性检测癌症的有前途的工具。

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