Evidence map›Paper›PMID 37391423›Full record

ArticleNature communications2023

Fast-exchanging spirocyclic rhodamine probes for aptamer-based super-resolution RNA imaging.

Daniel Englert, Eva-Maria Burger, Franziska Grün, Mrigank S Verma, Jens Lackner, Marko Lampe, Bastian Bühler, Janin Schokolowski, G Ulrich Nienhaus, Andres Jäschke and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
9.8field-weighted citation impact, top 1% of its field
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

19 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  12. Imaging methods to monitor and quantify cell differentiation.Frontiers in cell and developmental biology · 2025
    Review
  13. Super-Resolved Protein Imaging Using Bifunctional Light-Up Aptamers.Angewandte Chemie (International ed. in English) · 2024
    Article
  14. Article
  15. Structure-based insights into fluorogenic RNA aptamers.Acta biochimica et biophysica Sinica · 2024
    Review
  16. 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 at 3 institutions in 3 countries.

Daniel EnglertInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany.
Eva-Maria BurgerInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany.
Franziska GrünInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany.
Mrigank S VermaInstitute of Applied Physics (APH), Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.ORCID 0000-0001-8149-0774
Jens LacknerInstitute of Applied Physics (APH), Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.
Marko LampeAdvanced Light Microscopy Facility, European Molecular Biology Laboratory, Heidelberg, Germany.ORCID 0000-0002-4510-9048
Bastian BühlerInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-2990-4962
Janin SchokolowskiInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany.
G Ulrich NienhausInstitute of Applied Physics (APH), Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany. uli@uiuc.edu.ORCID 0000-0002-5027-3192
Andres JäschkeInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany. jaeschke@uni-hd.de.ORCID 0000-0002-4625-2655
Murat SunbulInstitute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Heidelberg, Germany. msunbul@uni-heidelberg.de.ORCID 0000-0001-5284-3884
Heidelberg University · DEKarlsruhe Institute of Technology · DEEuropean Molecular Biology Laboratory · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Live-cell RNA imaging with high spatial and temporal resolution remains a major challenge. Here we report the development of RhoBAST:SpyRho, a fluorescent light-up aptamer (FLAP) system ideally suited for visualizing RNAs in live or fixed cells with various advanced fluorescence microscopy modalities. Overcoming problems associated with low cell permeability, brightness, fluorogenicity, and signal-to-background ratio of previous fluorophores, we design a novel probe, SpyRho (Spirocyclic Rhodamine), which tightly binds to the RhoBAST aptamer. High brightness and fluorogenicity is achieved by shifting the equilibrium between spirolactam and quinoid. With its high affinity and fast ligand exchange, RhoBAST:SpyRho is a superb system for both super-resolution SMLM and STED imaging. Its excellent performance in SMLM and the first reported super-resolved STED images of specifically labeled RNA in live mammalian cells represent significant advances over other FLAPs. The versatility of RhoBAST:SpyRho is further demonstrated by imaging endogenous chromosomal loci and proteins.

Indexed as

Fluorescent DyesOligonucleotidesAnimalsIonophoresMammalsMicroscopy, FluorescenceRhodaminesRNAFluorescent DyesIonophoresOligonucleotidesRhodaminesRNA

Identifiers

PMID37391423
PMCPMC10313827
OpenAlexW4382775756

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.