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Compounds enhancing human sperm motility identified using a high-throughput phenotypic screening platform

View ORCID ProfileFranz S. Gruber, View ORCID ProfileZoe C. Johnston, View ORCID ProfileNeil R. Norcross, View ORCID ProfileIrene Georgiou, View ORCID ProfileCaroline Wilson, View ORCID ProfileKevin D. Read, View ORCID ProfileIan H. Gilbert, View ORCID ProfileJason R. Swedlow, View ORCID ProfileSarah Martins de Silva, View ORCID ProfileChristopher LR Barratt
doi: https://doi.org/10.1101/2021.09.14.460292
Franz S. Gruber
$National Phenotypic Screening Centre, School of Life Sciences, University of Dundee, Dundee DD1 5EH
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Zoe C. Johnston
∼Reproductive Medicine Research Group, Division of Systems Medicine, School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD19SY, UK
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Neil R. Norcross
‡Drug Discovery Unit, Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discover, University of Dundee, Dundee, DD1 5EH., UK
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Irene Georgiou
‡Drug Discovery Unit, Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discover, University of Dundee, Dundee, DD1 5EH., UK
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Caroline Wilson
‡Drug Discovery Unit, Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discover, University of Dundee, Dundee, DD1 5EH., UK
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Kevin D. Read
‡Drug Discovery Unit, Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discover, University of Dundee, Dundee, DD1 5EH., UK
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Ian H. Gilbert
‡Drug Discovery Unit, Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discover, University of Dundee, Dundee, DD1 5EH., UK
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Jason R. Swedlow
§University of Dundee, Division of Computational Biology and Centre for Gene Regulation and Expression, School of Life Sciences, Dundee, UK
$National Phenotypic Screening Centre, School of Life Sciences, University of Dundee, Dundee DD1 5EH
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Sarah Martins de Silva
∼Reproductive Medicine Research Group, Division of Systems Medicine, School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD19SY, UK
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Christopher LR Barratt
∼Reproductive Medicine Research Group, Division of Systems Medicine, School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD19SY, UK
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  • For correspondence: c.barratt@dundee.ac.uk
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Abstract

Study question Can a high-throughput screening platform facilitate male fertility drug discovery?

Summary answer A high-throughput screening platform identified a large number of compounds that enhanced sperm motility.

What is known already Several efforts to find small molecules modulating sperm function have been performed but not using high-throughput technology.

Study design, size, duration Healthy donor semen samples were used and samples were pooled (3-5 donors per pool). Primary screening was performed in singlicate; dose-response screening was performed in duplicate (independent donor pools).

Participants/materials, setting, methods Spermatozoa isolated from healthy donors were prepared by density gradient centrifugation and incubated in 384-well plates with compounds (6.25 uM) to identify those compounds with enhancing effects on motility. A total of ∼17,000 compounds from the following libraries: ReFRAME, Prestwick, Tocris, LOPAC, CLOUD and MMV Pathogen Box were screened. Dose response experiments of screening hits were performed to confirm the enhancing effect on sperm motility. Experiments were performed in a University setting.

Main results and the role of chance From our primary single concentration screening, 105 compounds elicited an enhancing effect on sperm motility compared to DMSO treated wells. Confirmed enhancing compounds were grouped based on their annotated targets/target classes. A major target class, phosphodiesterase inhibitors, were identified in particular PDE10A inhibitors as well as number of compounds not previously identified/known to enhance human sperm motility such as those related to GABA signaling.

Limitations, reasons for caution Compounds have been tested with prepared donor spermatozoa and only incubated for a short period of time. Therefore, the effect of compounds on whole semen or with longer incubation time may be different. All experiments were performed in vitro.

Wider implications of the findings This phenotypic screening assay identified a large number of compounds that increased sperm motility. In addition to furthering our understanding of human sperm function, for example identifying new avenues for discovery, we highlight potential inhibitors as promising start-point for a medicinal chemistry programme for potential enhancement of male infertility. Moreover, with disclosure of the results of screening we present a substantial resource to inform further work in the field

Study funding/competing interest(s) This study was supported by the Bill and Melinda Gates Foundation and Scottish Funding Council and Scottish Universities Life Science Alliance.

Competing Interest Statement

CLRB is Editor for RBMO. CLRB receives funding from Chief Scientists Office (Scotland), ESHRE and Genus PLC. No other authors declared a COI

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted September 16, 2021.
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Compounds enhancing human sperm motility identified using a high-throughput phenotypic screening platform
Franz S. Gruber, Zoe C. Johnston, Neil R. Norcross, Irene Georgiou, Caroline Wilson, Kevin D. Read, Ian H. Gilbert, Jason R. Swedlow, Sarah Martins de Silva, Christopher LR Barratt
bioRxiv 2021.09.14.460292; doi: https://doi.org/10.1101/2021.09.14.460292
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Compounds enhancing human sperm motility identified using a high-throughput phenotypic screening platform
Franz S. Gruber, Zoe C. Johnston, Neil R. Norcross, Irene Georgiou, Caroline Wilson, Kevin D. Read, Ian H. Gilbert, Jason R. Swedlow, Sarah Martins de Silva, Christopher LR Barratt
bioRxiv 2021.09.14.460292; doi: https://doi.org/10.1101/2021.09.14.460292

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