Evidence map›Paper›PMID 38922685›Full record

ArticleNucleic acids research2024

Multiplexed sequential imaging in living cells with orthogonal fluorogenic RNA aptamer/dye pairs.

Ru Zheng, Rigumula Wu, Yuanchang Liu, Zhining Sun, Zhaolin Xue, Yousef Bagheri, Sima Khajouei, Lan Mi, Qian Tian, Raymond Pho and 4 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Imaging methods to monitor and quantify cell differentiation.Frontiers in cell and developmental biology · 2025
    Review
  6. Optogenetic Tools for Regulating RNA Metabolism and Functions.Chembiochem : a European journal of chemical biology · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ru ZhengDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Rigumula WuDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Yuanchang LiuDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Zhining SunDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Zhaolin XueDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Yousef BagheriDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Sima KhajoueiDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Lan MiDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Qian TianDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Raymond PhoDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA 01003, USA.
Qinge LiuDepartment of Chemistry, Mount Holyoke College, Holyoke, MA 01075, USA.
Sidrat SiddiquiDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.ORCID 0009-0002-1361-9278
Kewei RenDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Mingxu YouDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.ORCID 0000-0003-3293-9760

Funding

Chemistry-Biology Interface Predoctoral Training GrantT32GM139789 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ERIC Robert STRIETER · 2021 to 2026
$3.4M
Alfred P. Sloan Research FellowshipCamille Dreyfus Teacher-Scholar AwardChan Zuckerberg Initiative Dynamic Imaging 2023-321170NIGMS NIH HHS T32 GM139789NIH HHS T32GM139789NSF 1846152Paul Hatheway Terry ScholarshipSLAS Graduate Education FellowshipUMass Amherst
6 · The paper itself

Abstract

Detecting multiple targets in living cells is important in cell biology. However, multiplexed fluorescence imaging beyond two-to-three targets remains a technical challenge. Herein, we introduce a multiplexed imaging strategy, 'sequential Fluorogenic RNA Imaging-Enabled Sensor' (seqFRIES), which enables live-cell target detection via sequential rounds of imaging-and-stripping. In seqFRIES, multiple orthogonal fluorogenic RNA aptamers are genetically encoded inside cells, and then the corresponding cell membrane permeable dye molecules are added, imaged, and rapidly removed in consecutive detection cycles. As a proof-of-concept, we have identified in this study four fluorogenic RNA aptamer/dye pairs that can be used for highly orthogonal and multiplexed imaging in living bacterial and mammalian cells. After further optimizing the cellular fluorescence activation and deactivation kinetics of these RNA/dye pairs, the whole four-color semi-quantitative seqFRIES process can be completed in ∼20 min. Meanwhile, seqFRIES-mediated simultaneous detection of critical signalling molecules and mRNA targets was also achieved within individual living cells. We expect our validation of this new seqFRIES concept here will facilitate the further development and potential broad usage of these orthogonal fluorogenic RNA/dye pairs for multiplexed and dynamic live-cell imaging and cell biology studies.

Indexed as

Aptamers, NucleotideFluorescent DyesHumansOptical ImagingRNAAptamers, NucleotideFluorescent DyesRNA

Identifiers

PMID38922685
PMCPMC11347136

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.