Evidence map›Paper›PMID 33637723›Full record

ArticleNature communications2021

Ultra-bright Raman dots for multiplexed optical imaging.

Zhilun Zhao, Chen Chen, Shixuan Wei, Hanqing Xiong, Fanghao Hu, Yupeng Miao, Tianwei Jin, Wei Min

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
13.2field-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

29 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
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  7. Review
  8. Principle of Stimulated Raman Scattering Microscopy: Emerging at High Spatiotemporal Limits.The journal of physical chemistry. C, Nanomaterials and interfaces · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. High-multiplex tissue imaging in routine pathology-are we there yet?Virchows Archiv : an international journal of pathology · 2023
    Review
  17. Article
  18. Toward the Next Frontiers of Vibrational Bioimaging.Chemical & biomedical imaging · 2023
    Review
  19. Design and Synthesis of SERS Materials for In Vivo Molecular Imaging and Biosensing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Zhilun Zhao *Department of Chemistry, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-1058-8173
Chen Chen *Department of Chemistry, Columbia University, New York, NY, USA.
Shixuan WeiDepartment of Chemistry, Columbia University, New York, NY, USA.
Hanqing XiongDepartment of Chemistry, Columbia University, New York, NY, USA.
Fanghao HuDepartment of Chemistry, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-8659-4027
Yupeng MiaoDepartment of Chemistry, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-7365-4828
Tianwei JinDepartment of Applied Physics and Applied Mathematics, Columbia University, New York, NY, USA.
Wei MinDepartment of Chemistry, Columbia University, New York, NY, USA. wm2256@columbia.edu.ORCID http://orcid.org/0000-0003-2570-3557
Columbia University · US

Funding

Super-multiplex vibrational imaging in living cellsR01GM128214 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MIN, WEI · 2018 to 2021
$1.5M
Ultrahigh-resolution and single-molecule stimulated Raman scattering (SRS) microscopyR01GM132860 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MIN, WEI · 2019 to 2022
$1.3M
NIGMS NIH HHS R01 GM128214NIGMS NIH HHS R01 GM132860
6 · The paper itself

Abstract

Imaging the spatial distribution of biomolecules is at the core of modern biology. The development of fluorescence techniques has enabled researchers to investigate subcellular structures with nanometer precision. However, multiplexed imaging, i.e. observing complex biological networks and interactions, is mainly limited by the fundamental 'spectral crowding' of fluorescent materials. Raman spectroscopy-based methods, on the other hand, have a much greater spectral resolution, but often lack the required sensitivity for practical imaging of biomarkers. Addressing the pressing need for new Raman probes, herein we present a series of Raman-active  nanoparticles (Rdots) that exhibit the combined advantages of ultra-brightness and compact sizes (~20 nm). When coupled with the emerging stimulated Raman scattering (SRS) microscopy, these Rdots are brighter than previously reported Raman-active organic probes by two to three orders of magnitude. We further obtain evidence supporting for SRS imaging of Rdots at single particle level. The compact size and ultra-brightness of Rdots allows immunostaining of specific protein targets (including cytoskeleton and low-abundant surface proteins) in mammalian cells and tissue slices with high imaging contrast. These Rdots thus offer a promising tool for a large range of studies on complex biological networks.

Indexed as

AnimalsBiomarkersChlorocebus aethiopsCOS CellsCytoskeletonHeLa CellsHumansMicroscopyNanoparticlesOptical ImagingSpectrum Analysis, RamanBiomarkers

Identifiers

PMID33637723
PMCPMC7910594
OpenAlexW3131570608

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.