Evidence map›Paper›PMID 38079451›Full record

ArticlePLoS biology2023

Protein nanobarcodes enable single-step multiplexed fluorescence imaging.

Daniëlle de Jong-Bolm, Mohsen Sadeghi, Cristian A Bogaciu, Guobin Bao, Gabriele Klaehn, Merle Hoff, Lucas Mittelmeier, F Buket Basmanav, Felipe Opazo, Frank Noé and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Simulating Multicolor Super-Resolution Imaging Using an RGB Camera.Computational and structural biotechnology journal · 2026
    Article
  2. Review
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 2 countries.

Daniëlle de Jong-BolmDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.ORCID 0000-0002-7422-1725
Mohsen SadeghiDepartment of Mathematics and Computer Science, Free University of Berlin, Berlin, Germany.ORCID 0000-0002-7698-5630
Cristian A BogaciuDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
Guobin BaoInstitute of Pharmacology and Toxicology, University Medical Center, Georg-August-University, Göttingen, Germany.
Gabriele KlaehnDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
Merle HoffDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
Lucas MittelmeierDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
F Buket BasmanavDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
Felipe OpazoDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
Frank NoéDepartment of Mathematics and Computer Science, Free University of Berlin, Berlin, Germany.
Silvio O RizzoliDepartment of Neuro- and Sensory physiology, University of Göttingen Medical Center, Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.
University of Göttingen · DEFreie Universität Berlin · DEMicrosoft (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiplexed cellular imaging typically relies on the sequential application of detection probes, as antibodies or DNA barcodes, which is complex and time-consuming. To address this, we developed here protein nanobarcodes, composed of combinations of epitopes recognized by specific sets of nanobodies. The nanobarcodes are read in a single imaging step, relying on nanobodies conjugated to distinct fluorophores, which enables a precise analysis of large numbers of protein combinations. Fluorescence images from nanobarcodes were used as input images for a deep neural network, which was able to identify proteins with high precision. We thus present an efficient and straightforward protein identification method, which is applicable to relatively complex biological assays. We demonstrate this by a multicell competition assay, in which we successfully used our nanobarcoded proteins together with neurexin and neuroligin isoforms, thereby testing the preferred binding combinations of multiple isoforms, in parallel.

Indexed as

Single-Domain AntibodiesAntibodiesDNAOptical ImagingProtein IsoformsAntibodiesDNAProtein IsoformsSingle-Domain Antibodies

Identifiers

PMID38079451
PMCPMC10735187
OpenAlexW4389547042

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.