Evidence map›Paper›PMID 25762511›Full record

ArticleScientific reports2015

In vivo X-ray elemental imaging of single cell model organisms manipulated by laser-based optical tweezers.

Eva Vergucht, Toon Brans, Filip Beunis, Jan Garrevoet, Maarten De Rijcke, Stephen Bauters, David Deruytter, Michiel Vandegehuchte, Ine Van Nieuwenhove, Colin Janssen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

4 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Three-dimensional optical trapping and orientation of microparticles for coherent X-ray diffraction imaging.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  3. Article
  4. Article
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

12 authors at 2 institutions in 2 countries.

Eva VerguchtX-ray Microspectroscopy and Imaging Group, Ghent University, Krijgslaan 281 (S12), B-9000 Ghent, Belgium.
Toon Brans1] Department of Electronics and Information Systems, Ghent University, Sint-Pietersnieuwstraat 41, B-9000 Ghent, Belgium [2] Center for Nano and Biophotonics, Ghent University, Sint-Pietersnieuwstraat 41, B-9000 Ghent, Belgium.
Filip Beunis1] Department of Electronics and Information Systems, Ghent University, Sint-Pietersnieuwstraat 41, B-9000 Ghent, Belgium [2] Center for Nano and Biophotonics, Ghent University, Sint-Pietersnieuwstraat 41, B-9000 Ghent, Belgium.
Jan GarrevoetX-ray Microspectroscopy and Imaging Group, Ghent University, Krijgslaan 281 (S12), B-9000 Ghent, Belgium.
Maarten De RijckeLaboratory of Environmental Toxicology and Aquatic Ecology, Ghent University, Jozef Plateaustraat 22, B-9000 Ghent, Belgium.
Stephen Bauters1] X-ray Microspectroscopy and Imaging Group, Ghent University, Krijgslaan 281 (S12), B-9000 Ghent, Belgium [2] European Synchrotron Radiation Facility, 71 avenue des Martyrs, F-38000 Grenoble, France.
David DeruytterLaboratory of Environmental Toxicology and Aquatic Ecology, Ghent University, Jozef Plateaustraat 22, B-9000 Ghent, Belgium.
Michiel VandegehuchteLaboratory of Environmental Toxicology and Aquatic Ecology, Ghent University, Jozef Plateaustraat 22, B-9000 Ghent, Belgium.
Ine Van NieuwenhovePolymer Chemistry and Biomaterials Group, Ghent University, Krijgslaan 281 (S4), B-9000 Ghent, Belgium.
Colin JanssenLaboratory of Environmental Toxicology and Aquatic Ecology, Ghent University, Jozef Plateaustraat 22, B-9000 Ghent, Belgium.
Manfred Burghammer1] European Synchrotron Radiation Facility, 71 avenue des Martyrs, F-38000 Grenoble, France [2] X-ray Microspectroscopy and Imaging Group, Ghent University, Krijgslaan 281 (S12), B-9000 Ghent, Belgium.
Laszlo VinczeX-ray Microspectroscopy and Imaging Group, Ghent University, Krijgslaan 281 (S12), B-9000 Ghent, Belgium.
Ghent University · BEEuropean Synchrotron Radiation Facility · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report on a radically new elemental imaging approach for the analysis of biological model organisms and single cells in their natural, in vivo state. The methodology combines optical tweezers (OT) technology for non-contact, laser-based sample manipulation with synchrotron radiation confocal X-ray fluorescence (XRF) microimaging for the first time. The main objective of this work is to establish a new method for in vivo elemental imaging in a two-dimensional (2D) projection mode in free-standing biological microorganisms or single cells, present in their aqueous environment. Using the model organism Scrippsiella trochoidea, a first proof of principle experiment at beamline ID13 of the European Synchrotron Radiation Facility (ESRF) demonstrates the feasibility of the OT XRF methodology, which is applied to study mixture toxicity of Cu-Ni and Cu-Zn as a result of elevated exposure. We expect that the new OT XRF methodology will significantly contribute to the new trend of investigating microorganisms at the cellular level with added in vivo capability.

Indexed as

MicroalgaeOptical TweezersSpectrometry, X-Ray EmissionComputer-Aided DesignEquipment Design

Identifiers

PMID25762511
PMCPMC4356986
OpenAlexW2070643015

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.