Turning high-throughput structural biology into predictive inhibitor design Journal Article
| Authors: | Saar, K. L.; McCorkindale, W.; Fearon, D.; Boby, M.; Barr, H.; Ben-Shmuel, A.; The COVID Moonshot Consortium; London, N.; von Delft, F.; Chodera, J. D.; Lee, A. A. |
| Article Title: | Turning high-throughput structural biology into predictive inhibitor design |
| Abstract: | A common challenge in drug design pertains to finding chemical modifications to a ligand that increases its affinity to the target protein. An underutilized advance is the increase in structural biology throughput, which has progressed from an artisanal endeavor to a monthly throughput of hundreds of different ligands against a protein in modern synchrotrons. However, the missing piece is a framework that turns high-throughput crystallography data into predictive models for ligand design. Here, we designed a simple machine learning approach that predicts protein- ligand affinity from experimental structures of diverse ligands against a single protein paired with biochemical measurements. Our key insight is using physics-based energy descriptors to represent protein-ligand complexes and a learning-to-rank approach that infers the relevant differences between binding modes. We ran a high-throughput crystallography campaign against the SARS-CoV-2 main protease (MPro), obtaining parallel measurements of over 200 protein-ligand complexes and their binding activities. This allows us to design one-step library syntheses which improved the potency of two distinct micromolar hits by over 10-fold, arriving at a noncovalent and nonpeptidomimetic inhibitor with 120 nM antiviral efficacy. Crucially, our approach successfully extends ligands to unexplored regions of the binding pocket, executing large and fruitful moves in chemical space with simple chemistry. © 2023 the Author(s). |
| Keywords: | drug design; crystallography; machine learning |
| Journal Title: | Proceedings of the National Academy of Sciences of the United States of America |
| Volume: | 120 |
| Issue: | 11 |
| ISSN: | 0027-8424 |
| Publisher: | National Academy of Sciences |
| Date Published: | 2023-03-14 |
| Start Page: | e2214168120 |
| Language: | English |
| DOI: | 10.1073/pnas.2214168120 |
| PROVIDER: | scopus |
| PUBMED: | 36877844 |
| PMCID: | PMC10089178 |
| DOI/URL: | |
| Notes: | Article -- Source: Scopus |
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