Evidence map›Paper›PMID 38638209›Full record

ArticleChemical science2024

Laser capture microdissection and native mass spectrometry for spatially-resolved analysis of intact protein assemblies in tissue.

James W Hughes, Emma K Sisley, Oliver J Hale, Helen J Cooper

Open access · diamondAbstract read
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Article in Chemical science, 2024. 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
1.4field-weighted citation impact, top 22% 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, 6 citations in OpenAlex.

  1. Article
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  4. 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

4 authors at 1 institution in 1 country.

James W HughesSchool of Biosciences, University of Birmingham Edgbaston Birmingham B15 2TT UK h.j.cooper@bham.ac.uk.ORCID https://orcid.org/0000-0001-6229-7880
Emma K SisleySchool of Biosciences, University of Birmingham Edgbaston Birmingham B15 2TT UK h.j.cooper@bham.ac.uk.ORCID https://orcid.org/0000-0001-8721-3348
Oliver J HaleSchool of Biosciences, University of Birmingham Edgbaston Birmingham B15 2TT UK h.j.cooper@bham.ac.uk.ORCID https://orcid.org/0000-0002-2286-5780
Helen J CooperSchool of Biosciences, University of Birmingham Edgbaston Birmingham B15 2TT UK h.j.cooper@bham.ac.uk.ORCID https://orcid.org/0000-0003-4590-9384
University of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, we have shown that native ambient mass spectrometry imaging allows the spatial mapping of folded proteins and their complexes in thin tissue sections. Subsequent top-down native ambient mass spectrometry of adjacent tissue section enables protein identification. The challenges associated with protein identification by this approach are (i) the low abundance of proteins in tissue and associated long data acquisition timescales and (ii) irregular spatial distributions which hamper targeted sampling of the relevant tissue location. Here, we demonstrate that these challenges may be overcome through integration of laser capture microdissection in the workflow. We show identification of intact protein assemblies in rat liver tissue and apply the approach to identification of proteins in the granular layer of rat cerebellum.

Identifiers

PMID38638209
PMCPMC11023061
OpenAlexW4392565796

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.