Evidence map›Paper›PMID 22645650›Full record

ArticleOpen biology2011

Labile disulfide bonds are common at the leucocyte cell surface.

Clive Metcalfe, Peter Cresswell, Laura Ciaccia, Benjamin Thomas, A Neil Barclay

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.2field-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

41 citing papers in PubMed, 79 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

5 authors at 4 institutions in 2 countries.

Clive MetcalfeSir William Dunn School of Pathology, University of Oxford , Oxford OX1 3RE, UK.
Peter Cresswell
Laura Ciaccia
Benjamin Thomas
A Neil Barclay
University of Oxford · GBHoward Hughes Medical Institute · USOxfam · GBYale University · US

Funding

Medical Research Council G0400808Medical Research Council G9826026
6 · The paper itself

Abstract

Redox conditions change in events such as immune and platelet activation, and during viral infection, but the biochemical consequences are not well characterized. There is evidence that some disulfide bonds in membrane proteins are labile while others that are probably structurally important are not exposed at the protein surface. We have developed a proteomic/mass spectrometry method to screen for and identify non-structural, redox-labile disulfide bonds in leucocyte cell-surface proteins. These labile disulfide bonds are common, with several classes of proteins being identified and around 30 membrane proteins regularly identified under different reducing conditions including using enzymes such as thioredoxin. The proteins identified include integrins, receptors, transporters and cell-cell recognition proteins. In many cases, at least one cysteine residue was identified by mass spectrometry as being modified by the reduction process. In some cases, functional changes are predicted (e.g. in integrins and cytokine receptors) but the scale of molecular changes in membrane proteins observed suggests that widespread effects are likely on many different types of proteins including enzymes, adhesion proteins and transporters. The results imply that membrane protein activity is being modulated by a 'redox regulator' mechanism.

Indexed as

Amino Acid SequenceAnimalsCell LineCell MembraneCysteineDisulfidesLeukocytesLipopolysaccharidesLymphocyte ActivationMass SpectrometryMembrane ProteinsMiceModels, MolecularMolecular Sequence DataOxidation-ReductionProteomicsCysteineDisulfidesLipopolysaccharidesMembrane Proteinsdisulfide bonds, membrane proteins, redox, leucocytes

Identifiers

PMID22645650
PMCPMC3352085
OpenAlexW2084771839

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.