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基于分子信标的成肌过程中多个 microRNAs 的生物成像。

Molecular beacon-based bioimaging of multiple microRNAs during myogenesis.

机构信息

Division of Nuclear Medicine, Department of Nuclear Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

出版信息

Biomaterials. 2011 Mar;32(7):1915-22. doi: 10.1016/j.biomaterials.2010.11.007. Epub 2010 Dec 3.

Abstract

MicroRNAs (miRNAs, miR) are associated with multiple cellular processes and diseases. Here, we designed fluorescent DNA probes composed of stem loop-structured DNA complementary to miRNAs and fluorophore-quencher pairs [molecular beacon (MB)] to simultaneously monitor the biogenesis of miR-206 and miR-26a, which are highly expressed during myogenic differentiation. C2C12 cells were transfected with an MB targeting miR-26a and containing a 6-FAM-BHQ1 pair (miRNA-26a MB) or an MB targeting miR-206 with a Texas Red-BHQ2 pair (miRNA-206 MB). In vitro and in vivo fluorescence analysis revealed that, only in differentiated single C2C12 cell, significantly increased fluorescence signals of miRNA-26a MB, miRNA-206 MB or simultaneous incubation of both beacons were detected due to the hybridization of miR-206 or miR-26a with their respective beacons, resulting in activation of fluorescence. Our MB-based miRNA imaging system may serve as a new imaging probe for monitoring multiple miRNAs during various cellular or disease processes associated with miRNAs.

摘要

微小 RNA(miRNAs,miR)与多种细胞过程和疾病有关。在这里,我们设计了由与 miRNAs 互补的茎环结构 DNA 组成的荧光 DNA 探针,并带有荧光团-猝灭剂对[分子信标(MB)],以同时监测 miR-206 和 miR-26a 的生物发生,这两种 miRNA 在肌生成分化过程中高度表达。将针对 miR-26a 并包含 6-FAM-BHQ1 对的 MB(miRNA-26a MB)或针对 miR-206 并包含 Texas Red-BHQ2 对的 MB(miRNA-206 MB)转染到 C2C12 细胞中。体外和体内荧光分析显示,仅在分化的单个 C2C12 细胞中,由于 miR-206 或 miR-26a 与各自的信标杂交,检测到 miRNA-26a MB、miRNA-206 MB 或同时孵育两种信标的荧光信号显著增加,从而激活了荧光。我们基于 MB 的 miRNA 成像系统可用作在与 miRNA 相关的各种细胞或疾病过程中监测多种 miRNA 的新型成像探针。

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