{"title":"从开放的 ADME 信息中有效整理膜渗透性数据的新工作流程。","authors":"Tsuyoshi Esaki, Tomoki Yonezawa, Kazuyoshi Ikeda","doi":"10.1186/s13321-024-00826-z","DOIUrl":null,"url":null,"abstract":"<div><p>Membrane permeability is an in vitro parameter that represents the apparent permeability (Papp) of a compound, and is a key absorption, distribution, metabolism, and excretion parameter in drug development. Although the Caco-2 cell lines are the most used cell lines to measure Papp, other cell lines, such as the Madin-Darby Canine Kidney (MDCK), LLC-Pig Kidney 1 (LLC-PK1), and Ralph Russ Canine Kidney (RRCK) cell lines, can also be used to estimate Papp. Therefore, constructing in silico models for Papp estimation using the MDCK, LLC-PK1, and RRCK cell lines requires collecting extensive amounts of in vitro Papp data. An open database offers extensive measurements of various compounds covering a vast chemical space; however, concerns were reported on the use of data published in open databases without the appropriate accuracy and quality checks. Ensuring the quality of datasets for training in silico models is critical because artificial intelligence (AI, including deep learning) was used to develop models to predict various pharmacokinetic properties, and data quality affects the performance of these models. Hence, careful curation of the collected data is imperative. Herein, we developed a new workflow that supports automatic curation of Papp data measured in the MDCK, LLC-PK1, and RRCK cell lines collected from ChEMBL using KNIME. The workflow consisted of four main phases. Data were extracted from ChEMBL and filtered to identify the target protocols. A total of 1661 high-quality entries were retained after checking 436 articles. The workflow is freely available, can be updated, and has high reusability. Our study provides a novel approach for data quality analysis and accelerates the development of helpful in silico models for effective drug discovery. Scientific Contribution: The cost of building highly accurate predictive models can be significantly reduced by automating the collection of reliable measurement data. Our tool reduces the time and effort required for data collection and will enable researchers to focus on constructing high-performance in silico models for other types of analysis. To the best of our knowledge, no such tool is available in the literature.</p></div>","PeriodicalId":617,"journal":{"name":"Journal of Cheminformatics","volume":"16 1","pages":""},"PeriodicalIF":7.1000,"publicationDate":"2024-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://jcheminf.biomedcentral.com/counter/pdf/10.1186/s13321-024-00826-z","citationCount":"0","resultStr":"{\"title\":\"A new workflow for the effective curation of membrane permeability data from open ADME information\",\"authors\":\"Tsuyoshi Esaki, Tomoki Yonezawa, Kazuyoshi Ikeda\",\"doi\":\"10.1186/s13321-024-00826-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Membrane permeability is an in vitro parameter that represents the apparent permeability (Papp) of a compound, and is a key absorption, distribution, metabolism, and excretion parameter in drug development. Although the Caco-2 cell lines are the most used cell lines to measure Papp, other cell lines, such as the Madin-Darby Canine Kidney (MDCK), LLC-Pig Kidney 1 (LLC-PK1), and Ralph Russ Canine Kidney (RRCK) cell lines, can also be used to estimate Papp. Therefore, constructing in silico models for Papp estimation using the MDCK, LLC-PK1, and RRCK cell lines requires collecting extensive amounts of in vitro Papp data. An open database offers extensive measurements of various compounds covering a vast chemical space; however, concerns were reported on the use of data published in open databases without the appropriate accuracy and quality checks. Ensuring the quality of datasets for training in silico models is critical because artificial intelligence (AI, including deep learning) was used to develop models to predict various pharmacokinetic properties, and data quality affects the performance of these models. Hence, careful curation of the collected data is imperative. Herein, we developed a new workflow that supports automatic curation of Papp data measured in the MDCK, LLC-PK1, and RRCK cell lines collected from ChEMBL using KNIME. The workflow consisted of four main phases. Data were extracted from ChEMBL and filtered to identify the target protocols. A total of 1661 high-quality entries were retained after checking 436 articles. The workflow is freely available, can be updated, and has high reusability. Our study provides a novel approach for data quality analysis and accelerates the development of helpful in silico models for effective drug discovery. Scientific Contribution: The cost of building highly accurate predictive models can be significantly reduced by automating the collection of reliable measurement data. Our tool reduces the time and effort required for data collection and will enable researchers to focus on constructing high-performance in silico models for other types of analysis. 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引用次数: 0
摘要
膜渗透性是一种体外参数,代表化合物的表观渗透性(Papp),是药物开发过程中一个关键的吸收、分布、代谢和排泄参数。虽然 Caco-2 细胞系是测量 Papp 最常用的细胞系,但其他细胞系,如 Madin-Darby 犬肾细胞系(MDCK)、LLC-猪肾 1 细胞系(LLC-PK1)和 Ralph Russ 犬肾细胞系(RRCK)也可用于估算 Papp。因此,使用 MDCK、LLC-PK1 和 RRCK 细胞系构建用于估算 Papp 的硅学模型需要收集大量的体外 Papp 数据。开放式数据库提供了涵盖广阔化学空间的各种化合物的大量测量数据;然而,有报告称,人们对使用开放式数据库中发布的数据而未进行适当的准确性和质量检查表示担忧。确保用于训练硅学模型的数据集的质量至关重要,因为人工智能(AI,包括深度学习)被用于开发预测各种药代动力学特性的模型,而数据质量会影响这些模型的性能。因此,仔细整理收集到的数据势在必行。在此,我们开发了一种新的工作流程,支持使用 KNIME 自动整理从 ChEMBL 收集的 MDCK、LLC-PK1 和 RRCK 细胞系中测量的 Papp 数据。工作流程包括四个主要阶段。从 ChEMBL 提取数据并过滤,以确定目标方案。在检查了 436 篇文章后,共保留了 1661 个高质量条目。该工作流程可免费获取、更新,并具有很高的可重用性。我们的研究为数据质量分析提供了一种新方法,并加快了有效药物发现的有用硅学模型的开发。科学贡献:通过自动收集可靠的测量数据,可以大大降低建立高精度预测模型的成本。我们的工具减少了数据收集所需的时间和精力,使研究人员能够集中精力构建高性能的硅学模型,用于其他类型的分析。据我们所知,文献中还没有这样的工具。
A new workflow for the effective curation of membrane permeability data from open ADME information
Membrane permeability is an in vitro parameter that represents the apparent permeability (Papp) of a compound, and is a key absorption, distribution, metabolism, and excretion parameter in drug development. Although the Caco-2 cell lines are the most used cell lines to measure Papp, other cell lines, such as the Madin-Darby Canine Kidney (MDCK), LLC-Pig Kidney 1 (LLC-PK1), and Ralph Russ Canine Kidney (RRCK) cell lines, can also be used to estimate Papp. Therefore, constructing in silico models for Papp estimation using the MDCK, LLC-PK1, and RRCK cell lines requires collecting extensive amounts of in vitro Papp data. An open database offers extensive measurements of various compounds covering a vast chemical space; however, concerns were reported on the use of data published in open databases without the appropriate accuracy and quality checks. Ensuring the quality of datasets for training in silico models is critical because artificial intelligence (AI, including deep learning) was used to develop models to predict various pharmacokinetic properties, and data quality affects the performance of these models. Hence, careful curation of the collected data is imperative. Herein, we developed a new workflow that supports automatic curation of Papp data measured in the MDCK, LLC-PK1, and RRCK cell lines collected from ChEMBL using KNIME. The workflow consisted of four main phases. Data were extracted from ChEMBL and filtered to identify the target protocols. A total of 1661 high-quality entries were retained after checking 436 articles. The workflow is freely available, can be updated, and has high reusability. Our study provides a novel approach for data quality analysis and accelerates the development of helpful in silico models for effective drug discovery. Scientific Contribution: The cost of building highly accurate predictive models can be significantly reduced by automating the collection of reliable measurement data. Our tool reduces the time and effort required for data collection and will enable researchers to focus on constructing high-performance in silico models for other types of analysis. To the best of our knowledge, no such tool is available in the literature.
期刊介绍:
Journal of Cheminformatics is an open access journal publishing original peer-reviewed research in all aspects of cheminformatics and molecular modelling.
Coverage includes, but is not limited to:
chemical information systems, software and databases, and molecular modelling,
chemical structure representations and their use in structure, substructure, and similarity searching of chemical substance and chemical reaction databases,
computer and molecular graphics, computer-aided molecular design, expert systems, QSAR, and data mining techniques.