Evidence map›Paper›PMID 32436764›Full record

ArticleSLAS discovery : advancing life sciences R & D2020

A High-Throughput Cellular Screening Assay for Small-Molecule Inhibitors and Activators of Cytoplasmic Dynein-1-Based Cargo Transport.

John Vincent, Marian Preston, Elizabeth Mouchet, Nicolas Laugier, Adam Corrigan, Jérôme Boulanger, Dean G Brown, Roger Clark, Mark Wigglesworth, Andrew P Carter and 1 more

Abstract read
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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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

11 authors.

John VincentHTS, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Macclesfield, Cheshire, UK.
Marian PrestonHTS, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Macclesfield, Cheshire, UK.
Elizabeth MouchetHTS, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Macclesfield, Cheshire, UK.
Nicolas LaugierDivision of Cell Biology, MRC Laboratory of Molecular Biology, Cambridge, Cambridgeshire, UK.
Adam CorriganQuantitative Biology, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Cambridge, Cambridgeshire, UK.
Jérôme BoulangerDivision of Cell Biology, MRC Laboratory of Molecular Biology, Cambridge, Cambridgeshire, UK.
Dean G BrownHit Discovery, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Boston, USA.
Roger ClarkDiscovery Biology, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Cambridge, Cambridgeshire, UK.
Mark WigglesworthHTS, Discovery Sciences, Bio Pharmaceuticals R&D, AstraZeneca, Macclesfield, Cheshire, UK.ORCID 0000-0002-6421-3414
Andrew P CarterDivision of Structural Studies, MRC Laboratory of Molecular Biology, Cambridge, Cambridgeshire, UK.
Simon L BullockDivision of Cell Biology, MRC Laboratory of Molecular Biology, Cambridge, Cambridgeshire, UK.

Funding

Medical Research Council MC_U105178790Medical Research Council MC_UP_A025_1011Wellcome Trust 210711/Z/18/Z
6 · The paper itself

Abstract

Cytoplasmic dynein-1 (hereafter dynein) is a six-subunit motor complex that transports a variety of cellular components and pathogens along microtubules. Dynein's cellular functions are only partially understood, and potent and specific small-molecule inhibitors and activators of this motor would be valuable for addressing this issue. It has also been hypothesized that an inhibitor of dynein-based transport could be used in antiviral or antimitotic therapy, whereas an activator could alleviate age-related neurodegenerative diseases by enhancing microtubule-based transport in axons. Here, we present the first high-throughput screening (HTS) assay capable of identifying both activators and inhibitors of dynein-based transport. This project is also the first collaborative screening report from the Medical Research Council and AstraZeneca agreement to form the UK Centre for Lead Discovery. A cellular imaging assay was used, involving chemically controlled recruitment of activated dynein complexes to peroxisomes. Such a system has the potential to identify molecules that affect multiple aspects of dynein biology in vivo. Following optimization of key parameters, the assay was developed in a 384-well format with semiautomated liquid handling and image acquisition. Testing of more than 500,000 compounds identified both inhibitors and activators of dynein-based transport in multiple chemical series. Additional analysis indicated that many of the identified compounds do not affect the integrity of the microtubule cytoskeleton and are therefore candidates to directly target the transport machinery.

Indexed as

Biological TransportCytoplasmic DyneinsHigh-Throughput Screening AssaysHumansIon TransportMicrotubulesPeroxisomesSmall Molecule LibrariesCytoplasmic DyneinsDYNC1H1 protein, humanSmall Molecule LibrariesdyneinHTSinducible cargo trafficking assaymicrotubules

Identifiers

PMID32436764
PMCPMC7116108

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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.