AFSE: towards improving model generalization of deep graph learning of ligand bioactivities targeting GPCR proteins. Issue 3 (25th March 2022)
- Record Type:
- Journal Article
- Title:
- AFSE: towards improving model generalization of deep graph learning of ligand bioactivities targeting GPCR proteins. Issue 3 (25th March 2022)
- Main Title:
- AFSE: towards improving model generalization of deep graph learning of ligand bioactivities targeting GPCR proteins
- Authors:
- Yin, Yueming
Hu, Haifeng
Yang, Zhen
Jiang, Feihu
Huang, Yihe
Wu, Jiansheng - Abstract:
- Abstract: Ligand molecules naturally constitute a graph structure. Recently, many excellent deep graph learning (DGL) methods have been proposed and used to model ligand bioactivities, which is critical for the virtual screening of drug hits from compound databases in interest. However, pharmacists can find that these well-trained DGL models usually are hard to achieve satisfying performance in real scenarios for virtual screening of drug candidates. The main challenges involve that the datasets for training models were small-sized and biased, and the inner active cliff cases would worsen model performance. These challenges would cause predictors to overfit the training data and have poor generalization in real virtual screening scenarios. Thus, we proposed a novel algorithm named adversarial feature subspace enhancement (AFSE). AFSE dynamically generates abundant representations in new feature subspace via bi-directional adversarial learning, and then minimizes the maximum loss of molecular divergence and bioactivity to ensure local smoothness of model outputs and significantly enhance the generalization of DGL models in predicting ligand bioactivities. Benchmark tests were implemented on seven state-of-the-art open-source DGL models with the potential of modeling ligand bioactivities, and precisely evaluated by multiple criteria. The results indicate that, on almost all 33 GPCRs datasets and seven DGL models, AFSE greatly improved their enhancement factor (top-10%, 20% andAbstract: Ligand molecules naturally constitute a graph structure. Recently, many excellent deep graph learning (DGL) methods have been proposed and used to model ligand bioactivities, which is critical for the virtual screening of drug hits from compound databases in interest. However, pharmacists can find that these well-trained DGL models usually are hard to achieve satisfying performance in real scenarios for virtual screening of drug candidates. The main challenges involve that the datasets for training models were small-sized and biased, and the inner active cliff cases would worsen model performance. These challenges would cause predictors to overfit the training data and have poor generalization in real virtual screening scenarios. Thus, we proposed a novel algorithm named adversarial feature subspace enhancement (AFSE). AFSE dynamically generates abundant representations in new feature subspace via bi-directional adversarial learning, and then minimizes the maximum loss of molecular divergence and bioactivity to ensure local smoothness of model outputs and significantly enhance the generalization of DGL models in predicting ligand bioactivities. Benchmark tests were implemented on seven state-of-the-art open-source DGL models with the potential of modeling ligand bioactivities, and precisely evaluated by multiple criteria. The results indicate that, on almost all 33 GPCRs datasets and seven DGL models, AFSE greatly improved their enhancement factor (top-10%, 20% and 30%), which is the most important evaluation in virtual screening of hits from compound databases, while ensuring the superior performance on RMSE and $r^2$ . The web server of AFSE is freely available at http://noveldelta.com/AFSE for academic purposes. … (more)
- Is Part Of:
- Briefings in bioinformatics. Volume 23:Issue 3(2022)
- Journal:
- Briefings in bioinformatics
- Issue:
- Volume 23:Issue 3(2022)
- Issue Display:
- Volume 23, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 23
- Issue:
- 3
- Issue Sort Value:
- 2022-0023-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-03-25
- Subjects:
- Genetics -- Data processing -- Periodicals
Molecular biology -- Data processing -- Periodicals
Genomes -- Data processing -- Periodicals
572.80285 - Journal URLs:
- http://bib.oxfordjournals.org ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1477-4054 ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1093/bib/bbac077 ↗
- Languages:
- English
- ISSNs:
- 1467-5463
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2283.958363
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21549.xml