Evidence map›Paper›PMID 32879402›Full record

ArticleScientific reports2020

Light sheet fluorescence microscopy guided MALDI-imaging mass spectrometry of cleared tissue samples.

Andreas Blutke, Na Sun, Zhihao Xu, Achim Buck, Luke Harrison, Sonja C Schriever, Paul T Pfluger, David Wiles, Thomas Kunzke, Katharina Huber and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

Andreas BlutkeResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Na SunResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Zhihao XuResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Achim BuckResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Luke HarrisonResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany.
Sonja C SchrieverResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany.
Paul T PflugerResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-8118-7588
David Wilesarivis AG, 80636, Munich, Germany.
Thomas KunzkeResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Katharina HuberResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Jürgen SchlegelInstitute for Pathology, Department of Neuropathology, Technische Universität München, 80333, Munich, Germany.
Michaela AichlerResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Annette FeuchtingerResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany. annette.feuchtinger@helmholtz-muenchen.de.
Kaspar MatiasekInstitute for Veterinary Pathology at the Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität München, 80539, Munich, Germany.
Stefanie M HauckResearch Unit for Protein Science, Helmholtz Zentrum München, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-1630-6827
Axel WalchResearch Unit Analytical Pathology, Helmholtz Zentrum München, 8576, Neuherberg, Germany.
Helmholtz Zentrum München · DELudwig-Maximilians-Universität München · DETechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Light sheet fluorescence microscopy (LSFM) of optically cleared biological samples represents a powerful tool to analyze the 3-dimensional morphology of tissues and organs. Multimodal combinations of LSFM with additional analyses of the identical sample help to limit the consumption of restricted specimen and reduce inter-sample variation. Here, we demonstrate the proof-of-concept that LSFM of cleared brain tissue samples can be combined with Matrix Assisted Laser Desorption/Ionization-Mass Spectrometry Imaging (MALDI-MSI) for detection and quantification of proteins. Samples of freshly dissected murine brain and of archived formalin-fixed paraffin-embedded (FFPE) human brain tissue were cleared (3DISCO). Tissue regions of interest were defined by LSFM and excised, (re)-embedded in paraffin, and sectioned. Mouse sections were coated with sinapinic acid matrix. Human brain sections were pre-digested with trypsin and coated with α-cyano-4-hydroxycinnamic acid matrix. Subsequently, sections were subjected to MALDI-time-of-flight (TOF)-MSI in mass ranges between 0.8 to 4 kDa (human tissue sections), or 2.5-25 kDa (mouse tissue sections) with a lateral resolution of 50 µm. Protein- and peptide-identities corresponding to acquired MALDI-MSI spectra were confirmed by parallel liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis. The spatial abundance- and intensity-patterns of established marker proteins detected by MALDI-MSI were also confirmed by immunohistochemistry.

Indexed as

AnimalsBrainFormaldehydeHumansImmunohistochemistryMiceParaffin EmbeddingPeptidesProteinsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTissue FixationTrypsinFormaldehydePeptidesProteinsTrypsin

Identifiers

PMID32879402
PMCPMC7468256
OpenAlexW3081970707

What OpenQuestion holds

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LicenceCC BY
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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.