Learning Subpocket Prototypes for Generalizable Structure-based Drug Design

被引:0
作者
Zhang, Zaixi [1 ,2 ]
Liu, Qi [1 ,2 ]
机构
[1] Univ Sci & Technol China, Anhui Prov Key Lab Big Data Anal & Applicat, Hefei, Peoples R China
[2] State Key Lab Cognit Intelligence, Hefei, Peoples R China
来源
INTERNATIONAL CONFERENCE ON MACHINE LEARNING, VOL 202 | 2023年 / 202卷
基金
中国国家自然科学基金;
关键词
MOLECULAR DOCKING; DISCOVERY; FRAGMENT;
D O I
暂无
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Generating molecules with high binding affinities to target proteins (a.k.a. structure-based drug design) is a fundamental and challenging task in drug discovery. Recently, deep generative models have achieved remarkable success in generating 3D molecules conditioned on the protein pocket. However, most existing methods consider molecular generation for protein pockets independently while neglecting the underlying connections such as subpocket-level similarities. Subpockets are the local protein environments of ligand fragments and pockets with similar subpockets may bind the same molecular fragment (motif) even though their overall structures are different. Therefore, the trained models can hardly generalize to unseen protein pockets in real-world applications. In this paper, we propose a novel method DrugGPS for generalizable structure-based drug design. With the biochemical priors, we propose to learn subpocket prototypes and construct a global interaction graph to model the interactions between subpocket prototypes and molecular motifs. Moreover, a hierarchical graph transformer encoder and motif-based 3D molecule generation scheme are used to improve the model's performance. The experimental results show that our model consistently outperforms baselines in generating realistic drug candidates with high affinities in challenging out-of-distribution settings.
引用
收藏
页数:17
相关论文
共 68 条
[1]   Fast, accurate, and reliable molecular docking with QuickVina 2 [J].
Alhossary, Amr ;
Handoko, Stephanus Daniel ;
Mu, Yuguang ;
Kwoh, Chee-Keong .
BIOINFORMATICS, 2015, 31 (13) :2214-2216
[2]   The process of structure-based drug design [J].
Anderson, AC .
CHEMISTRY & BIOLOGY, 2003, 10 (09) :787-797
[3]   Why is Tanimoto index an appropriate choice for fingerprint-based similarity calculations? [J].
Bajusz, David ;
Racz, Anita ;
Heberger, Kroly .
JOURNAL OF CHEMINFORMATICS, 2015, 7
[4]   An open source chemical structure curation pipeline using RDKit [J].
Bento, A. Patricia ;
Hersey, Anne ;
Felix, Eloy ;
Landrum, Greg ;
Gaulton, Anna ;
Atkinson, Francis ;
Bellis, Louisa J. ;
De Veij, Marleen ;
Leach, Andrew R. .
JOURNAL OF CHEMINFORMATICS, 2020, 12 (01)
[5]  
Blundell TL, 1996, NATURE, V384, P23
[6]   STABLE CALCULATION OF COORDINATES FROM DISTANCE INFORMATION [J].
CRIPPEN, GM ;
HAVEL, TF .
ACTA CRYSTALLOGRAPHICA SECTION A, 1978, 34 (MAR) :282-284
[7]   Vector Neurons: A General Framework for SO(3)-Equivariant Networks [J].
Deng, Congyue ;
Litany, Or ;
Duan, Yueqi ;
Poulenard, Adrien ;
Tagliasacchi, Andrea ;
Guibas, Leonidas .
2021 IEEE/CVF INTERNATIONAL CONFERENCE ON COMPUTER VISION (ICCV 2021), 2021, :12180-12189
[8]   Estimating the Similarity between Protein Pockets [J].
Eguida, Merveille ;
Rognan, Didier .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (20)
[9]   Target-Focused Library Design by Pocket-Applied Computer Vision and Fragment Deep Generative Linking [J].
Eguida, Merveille ;
Schmitt-Valencia, Christel ;
Hibert, Marcel ;
Villa, Pascal ;
Rognan, Didier .
JOURNAL OF MEDICINAL CHEMISTRY, 2022, 65 (20) :13771-13783
[10]   Molecular Docking and Structure-Based Drug Design Strategies [J].
Ferreira, Leonardo G. ;
dos Santos, Ricardo N. ;
Oliva, Glaucius ;
Andricopulo, Adriano D. .
MOLECULES, 2015, 20 (07) :13384-13421