Evidence map›Paper›PMID 38019733›Full record

ArticlePloS one2023

Validation of a highly sensitive HaloTag-based assay to evaluate the potency of a novel class of allosteric β-Galactosidase correctors.

Mikhail Rudinskiy, Maria Pons-Vizcarra, Tatiana Soldà, Ilaria Fregno, Timothy Jan Bergmann, Ana Ruano, Aida Delgado, Sara Morales, Xavier Barril, Manolo Bellotto and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Developing Allosteric Chaperones forInternational journal of molecular sciences · 2024
    Article
  5. 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 at 3 institutions in 2 countries.

Mikhail RudinskiyUniversità Della Svizzera Italiana, Lugano, Switzerland.
Maria Pons-VizcarraGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.ORCID 0000-0001-5008-5741
Tatiana SoldàUniversità Della Svizzera Italiana, Lugano, Switzerland.
Ilaria FregnoUniversità Della Svizzera Italiana, Lugano, Switzerland.
Timothy Jan BergmannUniversità Della Svizzera Italiana, Lugano, Switzerland.
Ana RuanoGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.
Aida DelgadoGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.
Sara MoralesGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.
Xavier BarrilGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.ORCID 0000-0002-0281-1347
Manolo BellottoGT Gain Therapeutics SA, Lugano, Switzerland.
Elena CuberoGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.ORCID 0000-0002-2239-6670
Ana María García-CollazoGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.
Natalia Pérez-CarmonaGain Therapeutics Sucursal en España, Parc Científic de Barcelona, Barcelona, Spain.
Maurizio MolinariUniversità Della Svizzera Italiana, Lugano, Switzerland.ORCID 0000-0002-7636-5829
Università della Svizzera italiana · CHÉcole Polytechnique Fédérale de Lausanne · CHInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Site-directed Enzyme Enhancement Therapy (SEE-Tx®) technology is a disease-agnostic drug discovery tool that can be applied to any protein target of interest with a known three-dimensional structure. We used this proprietary technology to identify and characterize the therapeutic potential of structurally targeted allosteric regulators (STARs) of the lysosomal hydrolase β-galactosidase (β-Gal), which is deficient due to gene mutations in galactosidase beta 1 (GLB1)-related lysosomal storage disorders (LSDs). The biochemical HaloTag cleavage assay was used to monitor the delivery of wildtype (WT) β-Gal and four disease-related β-Gal variants (p.Ile51Thr, p.Arg59His, p.Arg201Cys and p.Trp273Leu) in the presence and absence of two identified STAR compounds. In addition, the ability of STARs to reduce toxic substrate was assessed in a canine fibroblast cell model. In contrast to the competitive pharmacological chaperone N-nonyl-deoxygalactonojirimycin (NN-DGJ), the two identified STAR compounds stabilized and substantially enhanced the lysosomal transport of wildtype enzyme and disease-causing β-Gal variants. In addition, the two STAR compounds reduced the intracellular accumulation of exogenous GM1 ganglioside, an effect not observed with the competitive chaperone NN-DGJ. This proof-of-concept study demonstrates that the SEE-Tx® platform is a rapid and cost-effective drug discovery tool for identifying STARs for the treatment of LSDs. In addition, the HaloTag assay developed in our lab has proved valuable in investigating the effect of STARs in promoting enzyme transport and lysosomal delivery. Automatization and upscaling of this assay would be beneficial for screening STARs as part of the drug discovery process.

Indexed as

Gangliosidosis, GM1Lysosomal Storage Diseases1-DeoxynojirimycinAnimalsbeta-GalactosidaseDogsHydrolases1-Deoxynojirimycinbeta-Galactosidasehaloalkane dehalogenaseHydrolases

Identifiers

PMID38019733
PMCPMC10686464
OpenAlexW4389133111

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.