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用于哺乳动物细胞中RNA可视化的合成抗RNA抗体衍生物。

Synthetic anti-RNA antibody derivatives for RNA visualization in mammalian cells.

作者信息

Banna Hasan Al, Berg Kimberley, Sadat Tasnia, Das Naba Krishna, Paudel Roshan, D'Souza Victoria, Koirala Deepak

机构信息

Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.

Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkae1275.

Abstract

Although antibody derivatives, such as Fabs and scFvs, have revolutionized the cellular imaging, quantification and tracking of proteins, analogous tools and strategies are unavailable for cellular RNA visualization. Here, we developed four synthetic anti-RNA scFv (sarabody) probes and their green fluorescent protein (GFP) fusions and demonstrated their potential to visualize RNA in live mammalian cells. We expressed these sarabodies and sarabody-GFP modules, purified them as soluble proteins, characterized their binding interactions with their corresponding epitopes and finally employed two of the four modules, sara1-GFP and sara1c-GFP, to visualize a target messenger RNA in live U2OS cells. Our current RNA imaging strategy is analogous to the existing MCP-MS2 system for RNA visualization, but additionally, our approach provides robust flexibility for developing target RNA-specific imaging modules, as epitope-specific probes can be selected from a library generated by diversifying the sarabody complementarity determining regions. While we continue to optimize these probes, develop new probes for various target RNAs and incorporate other fluorescence proteins like mCherry and HaloTag, our groundwork results demonstrated that these first-of-a-kind immunofluorescent probes will have tremendous potential for tracking mature RNAs and may aid in visualizing and quantifying many cellular processes as well as examining the spatiotemporal dynamics of various RNAs.

摘要

尽管抗体衍生物,如Fab片段和单链抗体,已经彻底改变了蛋白质的细胞成像、定量和追踪,但类似的工具和策略在细胞RNA可视化方面却无法实现。在这里,我们开发了四种合成抗RNA单链抗体(sarabody)探针及其绿色荧光蛋白(GFP)融合体,并展示了它们在活的哺乳动物细胞中可视化RNA的潜力。我们表达了这些sarabody和sarabody-GFP模块,将它们作为可溶性蛋白进行纯化,表征了它们与相应表位的结合相互作用,最后使用四个模块中的两个,即sara1-GFP和sara1c-GFP,在活的U2OS细胞中可视化目标信使RNA。我们目前的RNA成像策略类似于现有的用于RNA可视化的MCP-MS2系统,但此外,我们的方法为开发靶标RNA特异性成像模块提供了强大的灵活性,因为可以从通过多样化sarabody互补决定区产生的文库中选择表位特异性探针。虽然我们继续优化这些探针,开发针对各种靶标RNA的新探针,并纳入其他荧光蛋白,如mCherry和HaloTag,但我们的基础研究结果表明,这些首创的免疫荧光探针在追踪成熟RNA方面将具有巨大潜力,并且可能有助于可视化和量化许多细胞过程以及研究各种RNA的时空动态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/852e/11879077/b05e952e95b8/gkae1275figgra1.jpg

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