Evidence map›Paper›PMID 37437308›Full record

ArticleBiochemistry2023

Computational Exploration of Potential CFTR Binding Sites for Type I Corrector Drugs.

Anna Lester, Madeline Sandman, Caitlin Herring, Christian Girard, Brandon Dixon, Havanna Ramsdell, Callista Reber, Jack Poulos, Alexis Mitchell, Allison Spinney and 4 more

Abstract read
In one paragraph

Article in Biochemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

14 authors.

Anna LesterBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.ORCID 0009-0005-0398-9277
Madeline SandmanBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Caitlin HerringBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Christian GirardBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Brandon DixonBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Havanna RamsdellBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Callista ReberBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Jack PoulosBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Alexis MitchellBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Allison SpinneyBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Marissa E HenagerBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Claudia N EvansBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.
Mark TurlingtonBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.ORCID 0000-0002-6126-0119
Quentin R JohnsonBerry College Department of Chemistry and Biochemistry, Mount Berry, Georgia 30149, United States.ORCID 0000-0002-2860-2877

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) is a recessive genetic disease that is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The recent development of a class of drugs called "correctors", which repair the structure and function of mutant CFTR, has greatly enhanced the life expectancy of CF patients. These correctors target the most common disease causing CFTR mutant F508del and are exemplified by the FDA-approved VX-809. While one binding site of VX-809 to CFTR was recently elucidated by cryo-electron microscopy, four additional binding sites have been proposed in the literature and it has been theorized that VX-809 and structurally similar correctors may engage multiple CFTR binding sites. To explore these five binding sites, ensemble docking was performed on wild-type CFTR and the F508del mutant using a large library of structurally similar corrector drugs, including VX-809 (lumacaftor), VX-661 (tezacaftor), ABBV-2222 (galicaftor), and a host of other structurally related molecules. For wild-type CFTR, we find that only one site, located in membrane spanning domain 1 (MSD1), binds favorably to our ligand library. While this MSD1 site also binds our ligand library for F508del-CFTR, the F508del mutation also opens a binding site in nucleotide binding domain 1 (NBD1), which enables strong binding of our ligand library to this site. This NBD1 site in F508del-CFTR exhibits the strongest overall binding affinity for our library of corrector drugs. This data may serve to better understand the structural changes induced by mutation of CFTR and how correctors bind to the protein. Additionally, it may aid in the design of new, more effective CFTR corrector drugs.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorAminopyridinesBenzodioxolesBinding SitesCryoelectron MicroscopyHumansLigandsMutationAminopyridinesBenzodioxolesCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorLigandslumacaftor

Identifiers

PMID37437308
PMCPMC10433520

What OpenQuestion holds

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Registered trials

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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.