Issue 1, 2023

Cell morphology-guided de novo hit design by conditioning GANs on phenotypic image features

Abstract

Developing novel bioactive molecules is time-consuming, costly and rarely successful. As a mitigation strategy, we utilize, for the first time, cellular morphology to directly guide the de novo design of small molecules. We trained a conditional generative adversarial network on a set of 30 000 compounds using their cell painting morphological profiles as conditioning. Our model was able to learn chemistry-morphology relationships and influence the generated chemical space according to the morphological profile. We provide evidence for the targeted generation of known agonists when conditioning on gene overexpression profiles, even though no information on biological targets was used during training. Based on a target-agnostic readout, our approach facilitates knowledge transfer between biological pathways and can be used to design bioactives for many targets under one unified framework. Prospective application of this proof-of-concept to larger chemical spaces promises great potential for hit generation in drug and phytopharmaceutical discovery and chemical safety.

Graphical abstract: Cell morphology-guided de novo hit design by conditioning GANs on phenotypic image features

Supplementary files

Article information

Article type
Paper
Submitted
03 Там. 2022
Accepted
18 Қар. 2022
First published
25 Қар. 2022
This article is Open Access
Creative Commons BY-NC license

Digital Discovery, 2023,2, 91-102

Cell morphology-guided de novo hit design by conditioning GANs on phenotypic image features

P. A. Marin Zapata, O. Méndez-Lucio, T. Le, C. J. Beese, J. Wichard, D. Rouquié and D. Clevert, Digital Discovery, 2023, 2, 91 DOI: 10.1039/D2DD00081D

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements