Evidence map›Paper›PMID 37918963›Full record

ArticleLife science alliance2024

CRISPR/Cas9 bioluminescence-based assay for monitoring CFTR trafficking to the plasma membrane.

Martin Ondra, Lukas Lenart, Amanda Centorame, Daciana C Dumut, Alexander He, Syeda Sadaf Zehra Zaidi, John W Hanrahan, Juan Bautista De Sanctis, Danuta Radzioch, Marian Hajduch

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

10 authors at 3 institutions in 2 countries.

Martin OndraInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0002-7661-3204
Lukas LenartInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
Amanda CentorameFaculty of Medicine and Health Sciences, McGill University, Montreal, Canada.
Daciana C DumutFaculty of Medicine and Health Sciences, McGill University, Montreal, Canada.
Alexander HePhysiology, McGill University, Montreal, Canada.
Syeda Sadaf Zehra ZaidiPhysiology, McGill University, Montreal, Canada.
John W HanrahanRI-MUHC, Montreal, Canada.ORCID https://orcid.org/0000-0001-9080-2039
Juan Bautista De SanctisInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0002-5480-4608
Danuta RadziochInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic danuta.radzioch@mcgill.ca.ORCID https://orcid.org/0000-0002-1601-2757
Marian HajduchInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic marian.hajduch@upol.cz.ORCID https://orcid.org/0000-0002-4834-908X
University Hospital Olomouc · CZMcGill University · CAMcGill University Health Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CFTR is a membrane protein that functions as an ion channel. Mutations that disrupt its biosynthesis, trafficking or function cause cystic fibrosis (CF). Here, we present a novel in vitro model system prepared using CRISPR/Cas9 genome editing with endogenously expressed WT-CFTR tagged with a HiBiT peptide. To enable the detection of CFTR in the plasma membrane of live cells, we inserted the HiBiT tag in the fourth extracellular loop of WT-CFTR. The 11-amino acid HiBiT tag binds with high affinity to a large inactive subunit (LgBiT), generating a reporter luciferase with bright luminescence. Nine homozygous clones with the HiBiT knock-in were identified from the 182 screened clones; two were genetically and functionally validated. In summary, this work describes the preparation and validation of a novel reporter cell line with the potential to be used as an ultimate building block for developing unique cellular CF models by CRISPR-mediated insertion of CF-causing mutations.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorCell LineCell MembraneCRISPR-Cas SystemsHumansCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID37918963
PMCPMC10622324
OpenAlexW4388214118

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.