Dijous 11 de juny, el Dipòsit Digital no estarà operatiu de 15:00 a 17:00 h per tasques de manteniment. Disculpeu les molèsties.
El jueves 11 de Junio, el Dipòsit Digital no estará operativo de 15:00 a 17:00 h debido a tareas de mantenimiento. Disculpen las molestias.
Thursday, Jun 11th, the Digital Repository will be unavailable due to a system update.

Document type

Article

Version

Published version

Publication date

Publication license

ccby-nc-nd (c) Elsevier
Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/207922

A machine learning and live-cell imaging tool kit uncovers small molecules induced phospholipidosis

Journal Title

Director/Tutor

Journal ISSN

Volume Title

Abstract

Drug-induced phospholipidosis (DIPL), characterized by excessive accumulation of phospholipids in lysosomes, can lead to clinical adverse effects. It may also alter phenotypic responses in functional studies using chemical probes. Therefore, robust methods are needed to predict and quantify phospholipidosis (PL) early in drug discovery and in chemical probe characterization. Here, we present a versatile high-content live-cell imaging approach, which was used to evaluate a chemogenomic and a lysosomal modulation library. We trained and evaluated several machine learning models using the most comprehensive set of publicly available compounds and interpreted the best model using SHapley Additive exPlanations (SHAP). Analysis of high-quality chemical probes extracted from the Chemical Probes Portal using our algorithm revealed that closely related molecules, such as chemical probes and their matched negative controls can differ in their ability to induce PL, highlighting the importance of identifying PL for robust target validation in chemical biology.

Subject (English)

Citation

Citation

HU, Huabin, et al. A machine learning and live-cell imaging tool kit uncovers small molecules induced phospholipidosis. Cell Chemical Biology. 2023. Vol. 30, num. 12, pags. 1634-1651. ISSN 2451-9448. [consulted: 11 of June of 2026]. Available at: https://hdl.handle.net/2445/207922

Export metadata

JSON - METS

Share record