journal article·2025-05-17Open access

ProLinker–Generator: Design of a PROTAC Linker Base on a Generation Model Using Transfer and Reinforcement Learning

Yanlin Luo, Danyang Song, Chengwei Zhang, An Su

Applied Sciences· Volume 15· Issue 10

Abstract

In PROTAC molecules, the design of the linker directly affects the formation efficiency and stability of the target protein–PROTAC–E3 ligase ternary complex, making it a critical factor in determining degradation activity. However, current linker data are limited, and the accessible chemical space remains narrow. The length, conformation, and chemical composition of linkers play a decisive role in drug performance, highlighting the urgent need for innovative linker design. In this study, we propose ProLinker-Generator, a GPT-based model aimed at generating novel and effective linkers. By integrating transfer learning and reinforcement learning, the model expands the chemical space of linkers and optimizes their design. During the transfer learning phase, the model achieved high scores in validity (0.989) and novelty (0.968) for the generated molecules. In the reinforcement learning phase, it further guided the generation of molecules with ideal properties within our predefined range. ProLinker-Generator demonstrates the significant potential of AI in linker design.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Protein Degradation and Inhibitors · Advancements in Semiconductor Devices and Circuit Design · Multiple Myeloma Research and Treatments

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, China

Zhejiang Key Laboratory of Green Manufacturing Technology for Chemical Drugs, Key Laboratory of Pharmaceutical Engineering of Zhejiang Province, Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education, College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China

Funding

Zhejiang Province Science and Technology Plan Project · National Natural Science Foundation of China · Joint Funds of the Zhejiang Provincial Natural Science Foundation of China

References (58)

Show source-provided references
1. Protacs: Great Opportunities for Academia and Industry10.1038/s41392-019-0101-6 ↗
2. Proteolysis-Targeting Chimeras: Induced Protein Degradation as a Therapeutic Strategy10.1021/acschembio.6b01068 ↗
3. Prime Time for Protacs10.1038/nchembio.1887 ↗
4. Targeted Intracellular Protein Degradation Induced by a Small Molecule: En Route to Chemical Proteomics10.1016/j.bmcl.2008.07.114 ↗
5. Targeted Protein Degradation: Advances in Drug Discovery and Clinical Practice10.1038/s41392-024-02004-x ↗
6. Protac Targeted Protein Degraders: The Past Is Prologue10.1038/s41573-021-00371-6 ↗
7. Small-Molecule Protacs: New Approaches to Protein Degradation10.1002/anie.201507978 ↗
8. Protein Degraders Enter the Clinic—A New Approach to Cancer Therapy10.1038/s41571-023-00736-3 ↗
9. Proteolysis-Targeting Chimeras (Protacs) in Cancer Therapy10.1186/s12943-021-01434-3 ↗
10. The Protac Technology in Drug Development10.1002/cbf.3369 ↗
11. From Conception to Development: Investigating Protacs Features for Improved Cell Permeability and Successful Protein Degradation10.3389/fchem.2021.672267 ↗
12. A Comprehensive Review of Emerging Approaches in Machine Learning Forde Novoprotac Design10.1039/D4DD00177J ↗
13. Modeling the Effect of Cooperativity in Ternary Complex Formation and Targeted Protein Degradation Mediated by Heterobifunctional Degraders10.1021/acsbiomedchemau.2c00037 ↗
14. Delineating the Role of Cooperativity in the Design of Potent Protacs for Btk10.1073/pnas.1803662115 ↗
15. Jamal, M.S., Song, K.-S., Lee, K.-W., Kim, J.-J., and Park, Y.-M. (2023). Revolutionizing Drug Targeting Strategies: Integrating Artificial Intelligence and Structure-Based Methods in Protac Development. Pharmaceuticals, 16.10.3390/ph16121649 ↗
16. Accelerated Rational Protac Design via Deep Learning and Molecular Simulations10.1038/s42256-022-00527-y ↗
17. Abbas, A., and Ye, F. (2024). Computational Methods and Key Considerations for in Silico Design of Proteolysis Targeting Chimera (Protacs). Int. J. Biol. Macromol., 277.10.1016/j.ijbiomac.2024.134293 ↗
18. Li, B., Ran, T., and Chen, H. (2023). 3d Based Generative Protac Linker Design with Reinforcement Learning. Brief. Bioinform., 24.10.1093/bib/bbad323 ↗
19. Predicting the Permeability of Macrocycles from Conformational Sampling—Limitations of Molecular Flexibility10.1016/j.xphs.2020.10.052 ↗
20. Constrained Graph Variational Autoencoders for Molecule Design
21. Molecular Generative Model Based on Conditional Variational Autoencoder for De Novo Molecular Design10.1186/s13321-018-0286-7 ↗
22. Automatic Chemical Design Using a Data-Driven Continuous Representation of Molecules10.1021/acscentsci.7b00572 ↗
23. Protac-Db: An Online Database of Protacs10.1093/nar/gkaa807 ↗
24. Deepprotacs Is a Deep Learning-Based Targeted Degradation Predictor for Protacs10.1038/s41467-022-34807-3 ↗
25. Molgpt: Molecular Generation Using a Transformer-Decoder Model10.1021/acs.jcim.1c00600 ↗
26. 3dsmiles-Gpt: 3d Molecular Pocket-Based Generation with Token-Only Large Language Model10.1039/D4SC06864E ↗
27. Rm-Gpt: Enhance the Comprehensive Generative Ability of Molecular Gpt Model via Localrnn and Realformer10.1016/j.artmed.2024.102827 ↗
28. Reinvent 2.0: An Ai Tool for De Novo Drug Design10.1021/acs.jcim.0c00915 ↗
29. Link-Invent: Generative Linker Design with Reinforcement Learning10.1039/D2DD00115B ↗
30. Acegen: Reinforcement Learning of Generative Chemical Agents for Drug Discovery10.1021/acs.jcim.4c00895 ↗
31. Polykovskiy, D., Zhebrak, A., Sanchez-Lengeling, B., Golovanov, S., Tatanov, O., Belyaev, S., Kurbanov, R., Artamonov, A., Aladinskiy, V., and Veselov, M. (2018). Molecular Sets (Moses): A Benchmarking Platform for Molecular Generation Models. Front. Pharmacol., 11.10.3389/fphar.2020.565644 ↗
32. The Chembl Database in 201710.1093/nar/gkw1074 ↗
33. Zinc: A Free Tool to Discover Chemistry for Biology10.1021/ci3001277 ↗
34. Moleculenet: A Benchmark for Molecular Machine Learning10.1039/C7SC02664A ↗
35. Prediction of Physicochemical Parameters by Atomic Contributions10.1021/ci990307l ↗
36. Estimation of Synthetic Accessibility Score of Drug-like Molecules Based on Molecular Complexity and Fragment Contributions10.1186/1758-2946-1-8 ↗
37. Quantifying the Chemical Beauty of Drugs10.1038/nchem.1243 ↗
38. Radford, A., Narasimhan, K., Salimans, T., and Sutskever, I. (2018). Improving Language Understanding by Generative Pre-Training.
39. Vaswani, A., Shazeer, N., Parmar, N., Uszkoreit, J., Jones, L., Gomez, A.N., Kaiser, L., and Polosukhin, I. (2017). Attention Is All You Need. Adv. Neural Inf. Process. Syst., 30.
40. Natural Language Processing Models That Automate Programming Will Transform Chemistry Research and Teaching10.1039/D1DD00009H ↗
41. Language Models Are Unsupervised Multitask Learners
42. Automoldesigner for Antibiotic Discovery: An Ai-Based Open-Source Software for Automated Design of Small-Molecule Antibiotics10.1021/acs.jcim.3c01562 ↗
43. Entangled Conditional Adversarial Autoencoder for De Novo Drug Discovery10.1021/acs.molpharmaceut.8b00839 ↗
44. Drugan: An Advanced Generative Adversarial Autoencoder Model for De Novo Generation of New Molecules with Desired Molecular Properties in Silico10.1021/acs.molpharmaceut.7b00346 ↗
45. Multi-Constraint Molecular Generation Based on Conditional Transformer, Knowledge Distillation and Reinforcement Learning10.1038/s42256-021-00403-1 ↗
46. Impact of Linker Length on the Activity of Protacs10.1039/C0MB00074D ↗
47. Unraveling the Role of Linker Design in Proteolysis Targeting Chimeras10.1021/acs.jmedchem.1c00482 ↗
48. Characteristic Roadmap of Linker Governs the Rational Design of Protacs10.1016/j.apsb.2024.04.007 ↗
49. Bjerrum, E.J. (2017). Smiles Enumeration as Data Augmentation for Neural Network Modeling of Molecules. arXiv.
50. Transfer Learning across Different Chemical Domains: Virtual Screening of Organic Materials with Deep Learning Models Pretrained on Small Molecule and Chemical Reaction Data10.1186/s13321-024-00886-1 ↗
51. Entezari, M., Wortsman, M., Saukh, O., Shariatnia, M., Sedghi, H., and Schmidt, L. (2023). The Role of Pre-Training Data in Transfer Learning. Comput. Sci.
52. Umap as a Dimensionality Reduction Tool for Molecular Dynamics Simulations of Biomacromolecules: A Comparison Study10.1021/acs.jpcb.1c02081 ↗
53. Umap: Uniform Manifold Approximation and Projection10.21105/joss.00861 ↗
54. Deep Generation Model Guided by the Docking Score for Active Molecular Design10.1021/acs.jcim.3c00572 ↗
55. Cb-Dock2: Improved Protein-Ligand Blind Docking by Integrating Cavity Detection, Docking and Homologous Template Fitting10.1093/nar/gkac394 ↗
56. Snapshots and Ensembles of Btk and Ciap1 Protein Degrader Ternary Complexes10.1038/s41589-020-00686-2 ↗
57. Generative Models for De Novo Drug Design10.1021/acs.jmedchem.1c00927 ↗
58. Generative Deep Learning for Targeted Compound Design10.1021/acs.jcim.0c01496 ↗