Evidence map›Paper›PMID 39739875›Full record

ArticleNucleic acids research2025

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

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

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Hasan Al BannaDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.ORCID 0000-0001-7475-6706
Kimberley BergDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Tasnia SadatDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.
Naba Krishna DasDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.ORCID 0000-0002-5308-2746
Roshan PaudelDepartment of Computer Science, Morgan State University, Baltimore, MD 21251, USA.ORCID 0000-0001-8134-8348
Victoria D'SouzaDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Deepak KoiralaDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.ORCID 0000-0001-6424-3173

Funding

Center for Structural Biology of HIV RNAU54AI170660 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALICE TELESNITSKY · 2022 to 2026
$32.1M
Graduate Training at The Chemistry Biology InterfaceT32GM066706 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SELEY-RADTKE, KATHERINE L, SMITH, AARON T · 2004 to 2023
$3.3M
Structural and mechanistic studies of cap-independent genome translation in (+)-strand RNA virusesR35GM150869 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI Deepak Koirala · 2023 to 2026
$1.4M
Division of Microbiology and Infectious Diseases NIH NIAID1U54AI170660NIAID NIH HHS U54 AI170660NIGMS NIH HHS 1R35GM150869NIGMS NIH HHS R35 GM150869NIGMS NIH HHS T32 GM066706
6 · The paper itself

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.

Indexed as

RNARNA, MessengerSingle-Chain AntibodiesAnimalsCell Line, TumorEpitopesGreen Fluorescent ProteinsHumansRecombinant Fusion ProteinsEpitopesGreen Fluorescent ProteinsRecombinant Fusion ProteinsRNARNA, MessengerSingle-Chain Antibodies

Identifiers

PMID39739875
PMCPMC11879077

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.