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Self-assembly of nucleic acid molecular aggregates catalyzed by a triple-helix probe for miRNA detection and single cell imaging

机译:三螺旋探针催化的核酸分子聚集体的自组装用于miRNA检测和单细胞成像

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摘要

We herein report a novel finding that nucleic acid molecular aggregates (NAMAs) self-assembled on graphene oxide nanoplates (GONPs) as a result of DNA rolling circle amplification (RCA) and a functionalized triple-helix probe (THP) in single cells. The functionalized THP containing the aptamer region for target recognition and the trigger DNA region for RCA was firstly used to activate RCA for miRNA imaging in single cells. Interestingly, NAMAs with the fluorescent labels were hybridized by both the RCA products and FAM-DNA, and could partly self-assemble on GONPs; meanwhile, NAMAs could extend from the GONPs, which led to the quenched fluorescence being renewed. Significantly, the NAMAs were successfully applied for low-abundance miRNA detection and imaging in single cells. The self-assembled NAMAs could generate prominent and agminated fluorescence-bright spots in single cancer cells, which will effectively drive cell imaging into a new era.
机译:我们在这里报告了一个新发现,即由于DNA滚环扩增(RCA)和功能化的三螺旋探针(THP)在单细胞中,核酸分子聚集体(NAMAs)自组装在氧化石墨烯纳米板上(GONPs)。包含用于靶标识别的适体区域和用于RCA的触发DNA区域的功能化THP首先用于激活RCA,以在单细胞中进行miRNA成像。有趣的是,带有荧光标记的NAMA可通过RCA产物和FAM-DNA杂交,并且可以在GONP上部分自组装。同时,NAMAs可能从GONPs延伸出来,导致淬灭的荧光得到更新。重要的是,NAMA已成功应用于单细胞低丰度miRNA检测和成像。自组装的NAMA可以在单个癌细胞中产生显着的,闪烁的荧光亮点,这将有效地推动细胞成像进入新时代。

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