利用目标评估、深度学习和自动实验室加速命中识别:IRAK1 的前瞻性验证。

IF 7.1 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Cheminformatics Pub Date : 2024-11-14 DOI:10.1186/s13321-024-00914-0
Gintautas Kamuntavičius, Alvaro Prat, Tanya Paquet, Orestis Bastas, Hisham Abdel Aty, Qing Sun, Carsten B. Andersen, John Harman, Marc E. Siladi, Daniel R. Rines, Sarah J. L. Flatters, Roy Tal, Povilas Norvaišas
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引用次数: 0

摘要

背景:通过应用生物医学知识分析、人工智能驱动的虚拟筛选和机器人云实验室系统,可以改变靶点识别和命中识别的方式。然而,很少有前瞻性研究对这种集成方法的功效进行评估:我们将自主开发的靶点评估(SpectraView)和深度学习驱动的虚拟筛选(HydraScreen)工具与专为超高通量筛选设计的自动化机器人云实验室进行了协同整合,从而使我们能够通过实验验证这些平台。通过使用目标评估工具选择 IRAK1 作为研究重点,我们对基于结构的深度学习模型进行了前瞻性验证。在排名前 1%的化合物中,我们可以识别出 23.8% 的 IRAK1 靶点。该模型优于传统的虚拟筛选技术,并提供配体姿态置信度评分等高级功能。同时,我们还从化合物库中发现了三个强效(纳摩尔)支架,其中两个代表了IRAK1的新型候选化合物,有望在未来得到开发:本研究为 SpectraView 和 HydraScreen 提供了令人信服的证据,可显著加快靶点识别和发现的过程。通过利用 Ro5 的 HydraScreen 和 Strateos 自动化实验室对 IRAK1 进行靶点识别,我们展示了利用 HydraScreen 进行人工智能驱动的虚拟筛选如何能够提供高靶点发现率并降低实验成本:我们提出了一个创新平台,该平台利用基于知识图谱的生物医学数据分析和人工智能驱动的虚拟筛选,并与机器人云实验室集成。通过无偏见的前瞻性评估,我们展示了HydraScreen在虚拟和高通量筛选中识别IRAK1基因突变的可靠性和稳健性。我们的平台和创新工具可以加速药物发现的早期阶段。
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Accelerated hit identification with target evaluation, deep learning and automated labs: prospective validation in IRAK1

Background

Target identification and hit identification can be transformed through the application of biomedical knowledge analysis, AI-driven virtual screening and robotic cloud lab systems. However there are few prospective studies that evaluate the efficacy of such integrated approaches.

Results

We synergistically integrate our in-house-developed target evaluation (SpectraView) and deep-learning-driven virtual screening (HydraScreen) tools with an automated robotic cloud lab designed explicitly for ultra-high-throughput screening, enabling us to validate these platforms experimentally. By employing our target evaluation tool to select IRAK1 as the focal point of our investigation, we prospectively validate our structure-based deep learning model. We can identify 23.8% of all IRAK1 hits within the top 1% of ranked compounds. The model outperforms traditional virtual screening techniques and offers advanced features such as ligand pose confidence scoring. Simultaneously, we identify three potent (nanomolar) scaffolds from our compound library, 2 of which represent novel candidates for IRAK1 and hold promise for future development.

Conclusion

This study provides compelling evidence for SpectraView and HydraScreen to provide a significant acceleration in the processes of target identification and hit discovery. By leveraging Ro5’s HydraScreen and Strateos’ automated labs in hit identification for IRAK1, we show how AI-driven virtual screening with HydraScreen could offer high hit discovery rates and reduce experimental costs.

Scientific contribution

We present an innovative platform that leverages Knowledge graph-based biomedical data analytics and AI-driven virtual screening integrated with robotic cloud labs. Through an unbiased, prospective evaluation we show the reliability and robustness of HydraScreen in virtual and high-throughput screening for hit identification in IRAK1. Our platforms and innovative tools can expedite the early stages of drug discovery.

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来源期刊
Journal of Cheminformatics
Journal of Cheminformatics CHEMISTRY, MULTIDISCIPLINARY-COMPUTER SCIENCE, INFORMATION SYSTEMS
CiteScore
14.10
自引率
7.00%
发文量
82
审稿时长
3 months
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.
期刊最新文献
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