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

IF 13.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleic Acids Research Pub Date : 2024-12-31 DOI:10.1093/nar/gkae1275
Hasan Al Banna, Kimberley Berg, Tasnia Sadat, Naba Krishna Das, Roshan Paudel, Victoria D'Souza, Deepak Koirala
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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.
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合成用于哺乳动物细胞RNA可视化的抗RNA抗体衍生物
虽然抗体衍生物,如fab和scFvs,已经彻底改变了细胞成像、定量和蛋白质跟踪,但类似的工具和策略无法用于细胞RNA可视化。在这里,我们开发了四种合成的抗RNA scFv (sarabody)探针及其绿色荧光蛋白(GFP)融合物,并证明了它们在活体哺乳动物细胞中可视化RNA的潜力。我们表达了这些sarabodies和sarabody-GFP模块,纯化了它们作为可溶性蛋白,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,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,我们的方法为开发目标RNA特异性成像模块提供了强大的灵活性,因为表位特异性探针可以从多样化的sarabody互补决定区域生成的文库中选择。当我们继续优化这些探针,为各种靶rna开发新的探针,并结合其他荧光蛋白如mCherry和HaloTag时,我们的基础研究结果表明,这些第一种免疫荧光探针将在跟踪成熟rna方面具有巨大的潜力,并可能有助于可视化和量化许多细胞过程,以及检查各种rna的时空动态。
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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