Evidence map›Paper›PMID 29426856›Full record

ArticleNature communications2018

Cellular imaging by targeted assembly of hot-spot SERS and photoacoustic nanoprobes using split-fluorescent protein scaffolds.

Tuğba Köker, Nathalie Tang, Chao Tian, Wei Zhang, Xueding Wang, Richard Martel, Fabien Pinaud

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 133 citations in OpenAlex.

  1. Review
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  10. Design and Synthesis of SERS Materials for In Vivo Molecular Imaging and Biosensing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  11. Article
  12. Silica Shell Thickness-Dependent Fluorescence Properties of SiOInternational journal of molecular sciences · 2022
    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

7 authors at 3 institutions in 2 countries.

Tuğba KökerDepartment of Biological Sciences, University of Southern California, 1050 Child Way, Los Angeles, CA, 90089, USA.
Nathalie TangDepartment of Chemistry, University of Montréal, C. P. 6128, Succursale Centre-Ville, Montréal, QC, H3C 3J7, Canada.
Chao TianDepartment of Biomedical Engineering, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, MI, 48109, USA.
Wei ZhangDepartment of Biomedical Engineering, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, MI, 48109, USA.
Xueding WangDepartment of Biomedical Engineering, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, MI, 48109, USA.
Richard MartelDepartment of Chemistry, University of Montréal, C. P. 6128, Succursale Centre-Ville, Montréal, QC, H3C 3J7, Canada.ORCID http://orcid.org/0000-0002-9021-4656
Fabien PinaudDepartment of Biological Sciences, University of Southern California, 1050 Child Way, Los Angeles, CA, 90089, USA. pinaud@usc.edu.ORCID http://orcid.org/0000-0002-4272-3616
University of Michigan · USUniversité de Montréal · CAUniversity of Southern California · US

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
Physiology of Inflammatory Arthritis in High ResolutionR01AR060350 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, XUEDING · 2011 to 2021
$6.0M
Photonic Nanosonophores for Functional and Structural ImagingR01CA186769 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOPELMAN, RAOUL, WANG, XUEDING · 2014 to 2018
$1.6M
NCI NIH HHS P30 CA014089NCI NIH HHS R01 CA186769NIAMS NIH HHS R01 AR060350
6 · The paper itself

Abstract

The in cellulo assembly of plasmonic nanomaterials into photo-responsive probes is of great interest for many bioimaging and nanophotonic applications but remains challenging with traditional nucleic acid scaffolds-based bottom-up methods. Here, we address this quandary using split-fluorescent protein (FP) fragments as molecular glue and switchable Raman reporters to assemble gold or silver plasmonic nanoparticles (NPs) into photonic clusters directly in live cells. When targeted to diffusing surface biomarkers in cancer cells, the NPs self-assemble into surface-enhanced Raman-scattering (SERS) nanoclusters having hot spots homogenously seeded by the reconstruction of full-length FPs. Within plasmonic hot spots, autocatalytic activation of the FP chromophore and near-field amplification of its Raman fingerprints enable selective and sensitive SERS imaging of targeted cells. This FP-driven assembly of metal colloids also yields enhanced photoacoustic signals, allowing the hybrid FP/NP nanoclusters to serve as contrast agents for multimodal SERS and photoacoustic microscopy with single-cell sensitivity.

Indexed as

Molecular ProbesAcousticsBiomarkers, TumorCatalysisColloidsDiffusionFluorescenceGoldGreen Fluorescent ProteinsHumansMetal NanoparticlesMicroscopyMicroscopy, Electron, TransmissionPhotoacoustic TechniquesSilverSpectrum Analysis, RamanBiomarkers, TumorColloidsGoldGreen Fluorescent ProteinsMolecular ProbesSilver

Identifiers

PMID29426856
PMCPMC5807522
OpenAlexW2805870691

What OpenQuestion holds

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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.