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基于力场和机器学习的打分函数在对开发帕金森病治疗药物有相关性的 MAO-B 蛋白抑制剂复合物的排序中的表现。

Performance of Force-Field- and Machine Learning-Based Scoring Functions in Ranking MAO-B Protein-Inhibitor Complexes in Relevance to Developing Parkinson's Therapeutics.

机构信息

Department of Theoretical Chemistry and Biology, School of Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, 10691 Stockholm, Sweden.

BiomAILS India Pvt Ltd., Hyderabad 500 090, India.

出版信息

Int J Mol Sci. 2020 Oct 16;21(20):7648. doi: 10.3390/ijms21207648.

DOI:10.3390/ijms21207648
PMID:33081086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7589968/
Abstract

Monoamine oxidase B (MAOB) is expressed in the mitochondrial membrane and has a key role in degrading various neurologically active amines such as benzylamine, phenethylamine and dopamine with the help of Flavin adenine dinucleotide (FAD) cofactor. The Parkinson's disease associated symptoms can be treated using inhibitors of MAO-B as the dopamine degradation can be reduced. Currently, many inhibitors are available having micromolar to nanomolar binding affinities. However, still there is demand for compounds with superior binding affinity and binding specificity with favorable pharmacokinetic properties for treating Parkinson's disease and computational screening methods can be majorly recruited for this. However, the accuracy of currently available force-field methods for ranking the inhibitors or lead drug-like compounds should be improved and novel methods for screening compounds need to be developed. We studied the performance of various force-field-based methods and data driven approaches in ranking about 3753 compounds having activity against the MAO-B target. The binding affinities computed using autodock and autodock-vina are shown to be non-reliable. The force-field-based MM-GBSA also under-performs. However, certain machine learning approaches, in particular KNN, are found to be superior, and we propose KNN as the most reliable approach for ranking the complexes to reasonable accuracy. Furthermore, all the employed machine learning approaches are also computationally less demanding.

摘要

单胺氧化酶 B(MAOB)表达在线粒体膜中,在黄素腺嘌呤二核苷酸(FAD)辅因子的帮助下,具有降解各种神经活性胺的关键作用,如苯乙胺、苯丙胺和多巴胺。使用 MAO-B 抑制剂可以治疗与帕金森病相关的症状,因为可以减少多巴胺的降解。目前,有许多具有微摩尔至纳摩尔结合亲和力的抑制剂可用。然而,仍然需要具有更高结合亲和力和结合特异性的化合物,以及具有良好药代动力学特性的化合物,以治疗帕金森病,计算筛选方法可以为此提供主要帮助。然而,目前可用的力场方法在对抑制剂或先导药物样化合物进行排序的准确性方面需要提高,并且需要开发用于筛选化合物的新方法。我们研究了各种基于力场的方法和数据驱动方法在对约 3753 种具有 MAO-B 靶标活性的化合物进行排序方面的性能。使用 autodock 和 autodock-vina 计算的结合亲和力被证明不可靠。基于力场的 MM-GBSA 也表现不佳。然而,某些机器学习方法,特别是 KNN,被发现具有优越性,我们提出 KNN 是对复合物进行排序以达到合理准确性的最可靠方法。此外,所有使用的机器学习方法在计算上的要求也较低。

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本文引用的文献

1
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J Chem Inf Model. 2020 Aug 24;60(8):3854-3863. doi: 10.1021/acs.jcim.0c00423. Epub 2020 Aug 13.
2
OnionNet: a Multiple-Layer Intermolecular-Contact-Based Convolutional Neural Network for Protein-Ligand Binding Affinity Prediction.洋葱网络:一种基于多层分子间接触的卷积神经网络,用于蛋白质-配体结合亲和力预测。
ACS Omega. 2019 Sep 16;4(14):15956-15965. doi: 10.1021/acsomega.9b01997. eCollection 2019 Oct 1.
3
Cross-interaction of tau PET tracers with monoamine oxidase B: evidence from in silico modelling and in vivo imaging.
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J Transl Med. 2023 Jun 12;21(1):380. doi: 10.1186/s12967-023-04233-0.
4
Exploring Scoring Function Space: Developing Computational Models for Drug Discovery.探索评分函数空间:开发药物发现的计算模型。
Curr Med Chem. 2024;31(17):2361-2377. doi: 10.2174/0929867330666230321103731.
5
Computationally Assisted Lead Optimization of Novel Potent and Selective MAO-B Inhibitors.新型强效和选择性单胺氧化酶-B抑制剂的计算机辅助先导优化
Biomedicines. 2021 Sep 24;9(10):1304. doi: 10.3390/biomedicines9101304.
tau PET 示踪剂与单胺氧化酶 B 的交叉相互作用:来自计算机建模和体内成像的证据。
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8
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9
Performance of the MM/GBSA scoring using a binding site hydrogen bond network-based frame selection: the protein kinase case.基于结合位点氢键网络的框架选择进行MM/GBSA评分的性能:蛋白激酶实例
Phys Chem Chem Phys. 2014 Jul 21;16(27):14047-58. doi: 10.1039/c4cp01378f. Epub 2014 Jun 5.
10
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J Cereb Blood Flow Metab. 2013 Jun;33(6):863-71. doi: 10.1038/jcbfm.2013.19. Epub 2013 Feb 13.