Evidence map›Paper›PMID 39779896›Full record

ReviewNature protocols2025

Sialic acid aptamer and RNA in situ hybridization-mediated proximity ligation assay for spatial imaging of glycoRNAs in single cells.

Weijie Guo, Yuan Ma, Quanbing Mou, Xiangli Shao, Mingkuan Lyu, Valeria Garcia, Linggen Kong, Whitney Lewis, Zhenglin Yang, Shuya Lu and 1 more

Abstract readReview
In one paragraph

Review in Nature protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
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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

11 authors.

Weijie Guo *Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.ORCID 0000-0001-5694-2142
Yuan Ma *Department of Chemistry, The University of Texas at Austin, Austin, TX, USA.
Quanbing MouDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.
Xiangli ShaoDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.
Mingkuan LyuDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.
Valeria GarciaDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.
Linggen KongDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.ORCID 0000-0003-4055-8626
Whitney LewisDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.ORCID 0000-0003-1203-6441
Zhenglin YangDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.
Shuya LuDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.ORCID 0009-0001-2767-4932
Yi LuInterdisciplinary Life Sciences Graduate Programs, The University of Texas at Austin, Austin, TX, USA. yi.lu@utexas.edu.ORCID 0000-0003-1221-6709

Funding

Design and Selection of Novel Metalloenzymes for Biocatalysis, Bioimaging, and Genetic EngineeringR35GM141931 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI Yi Lu · 2021 to 2026
$3.5M
NIGMS NIH HHS R35 GM141931U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) GM141931Welch Foundation F-0020
6 · The paper itself

Abstract

Glycosylated RNAs (glycoRNAs) have recently emerged as a new class of molecules of substantial interest owing to their potential roles in cellular processes and diseases. However, studying glycoRNAs is challenging owing to the lack of effective research tools including, but not limited to, imaging techniques to study the spatial distribution of glycoRNAs. Recently, we reported the development of a glycoRNA imaging technique, called sialic acid aptamer and RNA in situ hybridization-mediated proximity ligation assay (ARPLA), to visualize sialic acid-containing glycoRNAs with high sensitivity and specificity. Here we describe the experimental design principles and detailed step-by-step procedures for ARPLA-assisted glycoRNA imaging across multiple cell types. The procedure includes details for target selection, oligo design and preparation, optimized steps for RNA in situ hybridization, glycan recognition, proximity ligation, rolling circle amplification and a guideline for image acquisition and analysis. With properly designed probe sets and cells prepared, ARPLA-based glycoRNA imaging can typically be completed within 1 d by users with expertise in biochemistry and fluorescence microscopy. The ARPLA approach enables researchers to explore the spatial distribution, trafficking and functional contributions of glycoRNAs in various cellular processes.

Indexed as

Aptamers, NucleotideIn Situ HybridizationN-Acetylneuraminic AcidRNASingle-Cell AnalysisAnimalsGlycosylationHumansAptamers, NucleotideN-Acetylneuraminic AcidRNA

Identifiers

PMID39779896
PMCPMC12234808

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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.