利用可解释的机器学习和形态剖析细胞绘画数据识别溶酶体运动

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics
MedChemComm Pub Date : 2024-05-24 DOI:10.1039/D4MD00107A
Aishvarya Tandon, Anna Santura, Herbert Waldmann, Axel Pahl and Paul Czodrowski
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引用次数: 0

摘要

溶酶体促进作用是一种具有不同化学结构和主要作用靶点的化合物所具有的特性,因此是一种具有不同制药意义的现象。据报道,溶酶体倾向性主要是由具有适当亲脂性和碱性值的化合物引起的,但事实上并非所有符合这些标准的化合物都具有溶酶体倾向性。在这里,我们通过细胞涂色试验(CPA)进行形态分析,以此作为鉴定溶酶体促进性的可靠替代方法。我们注意到,在理化性质匹配的化合物子集中,只有 35% 显示出溶酶体向性表型。根据匹配分子对分析(MMPA),无法确定驱动溶酶体向性的关键亚结构。不过,利用可解释的机器学习(XML),我们能够在该子集的化合物中强调较高的亲脂性、碱性、分子量和较低的拓扑极性表面积是诱导溶酶体向性的重要特性之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identification of lysosomotropism using explainable machine learning and morphological profiling cell painting data†

Identification of lysosomotropism using explainable machine learning and morphological profiling cell painting data†

Identification of lysosomotropism using explainable machine learning and morphological profiling cell painting data†

Lysosomotropism is a phenomenon of diverse pharmaceutical interests because it is a property of compounds with diverse chemical structures and primary targets. While it is primarily reported to be caused by compounds having suitable lipophilicity and basicity values, not all compounds that fulfill such criteria are in fact lysosomotropic. Here, we use morphological profiling by means of the cell painting assay (CPA) as a reliable surrogate to identify lysosomotropism. We noticed that only 35% of the compound subset with matching physicochemical properties show the lysosomotropic phenotype. Based on a matched molecular pair analysis (MMPA), no key substructures driving lysosomotropism could be identified. However, using explainable machine learning (XML), we were able to highlight that higher lipophilicity, basicity, molecular weight, and lower topological polar surface area are among the important properties that induce lysosomotropism in the compounds of this subset.

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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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