Evidence map›Paper›PMID 33430309›Full record

ReviewInternational journal of molecular sciences2021

Mapping the SARS-CoV-2-Host Protein-Protein Interactome by Affinity Purification Mass Spectrometry and Proximity-Dependent Biotin Labeling: A Rational and Straightforward Route to Discover Host-Directed Anti-SARS-CoV-2 Therapeutics.

Rosa Terracciano, Mariaimmacolata Preianò, Annalisa Fregola, Corrado Pelaia, Tiziana Montalcini, Rocco Savino

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 46 citations in OpenAlex.

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  17. Thapsigargin: key to new host-directed coronavirus antivirals?Trends in pharmacological sciences · 2022
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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

6 authors at 1 institution in 1 country.

Rosa TerraccianoDepartment of Experimental and Clinical Medicine, University "Magna Græcia", 88100 Catanzaro, Italy.
Mariaimmacolata PreianòDepartment of Health Sciences, University "Magna Græcia", 88100 Catanzaro, Italy.
Annalisa FregolaDepartment of Health Sciences, University "Magna Græcia", 88100 Catanzaro, Italy.
Corrado PelaiaRespiratory Medicine Unit, University "Magna Græcia", 88100 Catanzaro, Italy.ORCID 0000-0002-4236-7367
Tiziana MontalciniDepartment of Experimental and Clinical Medicine, University "Magna Græcia", 88100 Catanzaro, Italy.ORCID 0000-0001-7048-5830
Rocco SavinoDepartment of Medical and Surgical Sciences, University "Magna Græcia", 88100 Catanzaro, Italy.
Magna Graecia University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-protein interactions (PPIs) are the vital engine of cellular machinery. After virus entry in host cells the global organization of the viral life cycle is strongly regulated by the formation of virus-host protein interactions. With the advent of high-throughput -omics platforms, the mirage to obtain a "high resolution" view of virus-host interactions has come true. In fact, the rapidly expanding approaches of mass spectrometry (MS)-based proteomics in the study of PPIs provide efficient tools to identify a significant number of potential drug targets. Generation of PPIs maps by affinity purification-MS and by the more recent proximity labeling-MS may help to uncover cellular processes hijacked and/or altered by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), providing promising therapeutic targets. The possibility to further validate putative key targets from high-confidence interactions between viral bait and host protein through follow-up MS-based multi-omics experiments offers an unprecedented opportunity in the drug discovery pipeline. In particular, drug repurposing, making use of already existing approved drugs directly targeting these identified and validated host interactors, might shorten the time and reduce the costs in comparison to the traditional drug discovery process. This route might be promising for finding effective antiviral therapeutic options providing a turning point in the fight against the coronavirus disease-2019 (COVID-19) outbreak.

Indexed as

COVID-19 Drug TreatmentProtein Interaction MapsA549 CellsAngiotensin-Converting Enzyme 2Antiviral AgentsCell LineCOVID-19Drug RepositioningHEK293 CellsHumansMass SpectrometryProtein Interaction MappingSARS-CoV-2Serine EndopeptidasesSpike Glycoprotein, CoronavirusVirus InternalizationACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsSerine EndopeptidasesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2TMPRSS2 protein, humanaffinity-purification mass spectrometryantiviralCOVID-19drug repurposingemergingprotein–protein interactionproteomicsproximity-dependent biotin labeling (BioID)SARS-CoV-2virus

Identifiers

PMID33430309
PMCPMC7825748
OpenAlexW3120373667

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.