Evidence map›Paper›PMID 35156780›Full record

ArticleMolecular systems biology2022

CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system.

Sang Hyun Lim, Jamie Snider, Liron Birimberg-Schwartz, Wan Ip, Joana C Serralha, Hugo M Botelho, Miquéias Lopes-Pacheco, Madalena C Pinto, Mohamed Taha Moutaoufik, Mara Zilocchi and 19 more

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

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  12. ACS pharmacology & translational science · 2023
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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

29 authors at 6 institutions in 5 countries.

Sang Hyun Lim *Donnelly Centre, University of Toronto, Toronto, ON, Canada.ORCID 0000-0003-0356-1295
Jamie Snider *Donnelly Centre, University of Toronto, Toronto, ON, Canada.
Liron Birimberg-SchwartzProgramme in Translational Medicine, The Hospital for Sick Children, Toronto, ON, Canada.
Wan IpProgramme in Translational Medicine, The Hospital for Sick Children, Toronto, ON, Canada.ORCID 0000-0001-9668-4360
Joana C SerralhaFaculty of Sciences, BioISI-Biosystems and Integrative Sciences Institute, University of Lisboa, Lisboa, Portugal.
Hugo M BotelhoFaculty of Sciences, BioISI-Biosystems and Integrative Sciences Institute, University of Lisboa, Lisboa, Portugal.ORCID 0000-0002-4208-1086
Miquéias Lopes-PachecoFaculty of Sciences, BioISI-Biosystems and Integrative Sciences Institute, University of Lisboa, Lisboa, Portugal.ORCID 0000-0002-7444-9359
Madalena C PintoFaculty of Sciences, BioISI-Biosystems and Integrative Sciences Institute, University of Lisboa, Lisboa, Portugal.ORCID 0000-0001-9045-269X
Mohamed Taha MoutaoufikDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, SK, Canada.ORCID 0000-0002-2013-1601
Mara ZilocchiDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, SK, Canada.
Onofrio LaselvaDepartment of Physiology, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-0237-4079
Mohsen EsmaeiliProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Max KotlyarOsteoarthritis Research Program, Division of Orthopedic Surgery, Schroeder Arthritis Institute, University Health Network, Toronto, ON, Canada.
Anna LyakishevaDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Priscilla TangDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Lucía López VázquezDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Indira AkulaDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Farzaneh AboualizadehDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Victoria WongDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Ingrid GrozavuDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Teuta Opacak-BernardiFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia.ORCID 0000-0001-8563-8684
Zhong YaoDonnelly Centre, University of Toronto, Toronto, ON, Canada.
Meg MendozaDepartment of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
Mohan BabuDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, SK, Canada.ORCID 0000-0003-4118-6406
Igor JurisicaOsteoarthritis Research Program, Division of Orthopedic Surgery, Schroeder Arthritis Institute, University Health Network, Toronto, ON, Canada.
Tanja GonskaProgramme in Translational Medicine, The Hospital for Sick Children, Toronto, ON, Canada.
Christine E BearDepartment of Biochemistry, University of Toronto, Toronto, ON, Canada.ORCID 0000-0001-7063-3418
Margarida D AmaralFaculty of Sciences, BioISI-Biosystems and Integrative Sciences Institute, University of Lisboa, Lisboa, Portugal.
Igor StagljarDonnelly Centre, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-5260-3327
University of Toronto · CAUniversity of Lisbon · PTUniversity of Regina · CAHospital for Sick Children · CAUniversity Health Network · CAUniversity of Osijek · HR

Funding

Canadian Institutes for Health Research 420989CIHR FDN-154318CIHR MSH-130178
6 · The paper itself

Abstract

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a chloride and bicarbonate channel in secretory epithelia with a critical role in maintaining fluid homeostasis. Mutations in CFTR are associated with Cystic Fibrosis (CF), the most common lethal autosomal recessive disorder in Caucasians. While remarkable treatment advances have been made recently in the form of modulator drugs directly rescuing CFTR dysfunction, there is still considerable scope for improvement of therapeutic effectiveness. Here, we report the application of a high-throughput screening variant of the Mammalian Membrane Two-Hybrid (MaMTH-HTS) to map the protein-protein interactions of wild-type (wt) and mutant CFTR (F508del), in an effort to better understand CF cellular effects and identify new drug targets for patient-specific treatments. Combined with functional validation in multiple disease models, we have uncovered candidate proteins with potential roles in CFTR function/CF pathophysiology, including Fibrinogen Like 2 (FGL2), which we demonstrate in patient-derived intestinal organoids has a significant effect on CFTR functional expression.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorAnimalsCell MembraneFibrinogenHigh-Throughput Screening AssaysHumansMammalsMutationCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorFGL2 protein, humanFibrinogencystic fibrosishigh-throughput screeningintegrative computational biologyinteractomemammalian membrane two-hybrid

Identifiers

PMID35156780
PMCPMC8842165
OpenAlexW4212926436

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.