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Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation
A plethora of AI-based techniques now exists to conduct de novo molecule generation that can devise molecules conditioned towards a particular endpoint in the context of drug design. One popular approach is using reinforcement learning to update a recurrent neural network or language-based de novo m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531503/ https://www.ncbi.nlm.nih.gov/pubmed/36192789 http://dx.doi.org/10.1186/s13321-022-00646-z |
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author | Thomas, Morgan O’Boyle, Noel M. Bender, Andreas de Graaf, Chris |
author_facet | Thomas, Morgan O’Boyle, Noel M. Bender, Andreas de Graaf, Chris |
author_sort | Thomas, Morgan |
collection | PubMed |
description | A plethora of AI-based techniques now exists to conduct de novo molecule generation that can devise molecules conditioned towards a particular endpoint in the context of drug design. One popular approach is using reinforcement learning to update a recurrent neural network or language-based de novo molecule generator. However, reinforcement learning can be inefficient, sometimes requiring up to 10(5) molecules to be sampled to optimize more complex objectives, which poses a limitation when using computationally expensive scoring functions like docking or computer-aided synthesis planning models. In this work, we propose a reinforcement learning strategy called Augmented Hill-Climb based on a simple, hypothesis-driven hybrid between REINVENT and Hill-Climb that improves sample-efficiency by addressing the limitations of both currently used strategies. We compare its ability to optimize several docking tasks with REINVENT and benchmark this strategy against other commonly used reinforcement learning strategies including REINFORCE, REINVENT (version 1 and 2), Hill-Climb and best agent reminder. We find that optimization ability is improved ~ 1.5-fold and sample-efficiency is improved ~ 45-fold compared to REINVENT while still delivering appealing chemistry as output. Diversity filters were used, and their parameters were tuned to overcome observed failure modes that take advantage of certain diversity filter configurations. We find that Augmented Hill-Climb outperforms the other reinforcement learning strategies used on six tasks, especially in the early stages of training or for more difficult objectives. Lastly, we show improved performance not only on recurrent neural networks but also on a reinforcement learning stabilized transformer architecture. Overall, we show that Augmented Hill-Climb improves sample-efficiency for language-based de novo molecule generation conditioning via reinforcement learning, compared to the current state-of-the-art. This makes more computationally expensive scoring functions, such as docking, more accessible on a relevant timescale. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-022-00646-z. |
format | Online Article Text |
id | pubmed-9531503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-95315032022-10-05 Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation Thomas, Morgan O’Boyle, Noel M. Bender, Andreas de Graaf, Chris J Cheminform Research A plethora of AI-based techniques now exists to conduct de novo molecule generation that can devise molecules conditioned towards a particular endpoint in the context of drug design. One popular approach is using reinforcement learning to update a recurrent neural network or language-based de novo molecule generator. However, reinforcement learning can be inefficient, sometimes requiring up to 10(5) molecules to be sampled to optimize more complex objectives, which poses a limitation when using computationally expensive scoring functions like docking or computer-aided synthesis planning models. In this work, we propose a reinforcement learning strategy called Augmented Hill-Climb based on a simple, hypothesis-driven hybrid between REINVENT and Hill-Climb that improves sample-efficiency by addressing the limitations of both currently used strategies. We compare its ability to optimize several docking tasks with REINVENT and benchmark this strategy against other commonly used reinforcement learning strategies including REINFORCE, REINVENT (version 1 and 2), Hill-Climb and best agent reminder. We find that optimization ability is improved ~ 1.5-fold and sample-efficiency is improved ~ 45-fold compared to REINVENT while still delivering appealing chemistry as output. Diversity filters were used, and their parameters were tuned to overcome observed failure modes that take advantage of certain diversity filter configurations. We find that Augmented Hill-Climb outperforms the other reinforcement learning strategies used on six tasks, especially in the early stages of training or for more difficult objectives. Lastly, we show improved performance not only on recurrent neural networks but also on a reinforcement learning stabilized transformer architecture. Overall, we show that Augmented Hill-Climb improves sample-efficiency for language-based de novo molecule generation conditioning via reinforcement learning, compared to the current state-of-the-art. This makes more computationally expensive scoring functions, such as docking, more accessible on a relevant timescale. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-022-00646-z. Springer International Publishing 2022-10-03 /pmc/articles/PMC9531503/ /pubmed/36192789 http://dx.doi.org/10.1186/s13321-022-00646-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Thomas, Morgan O’Boyle, Noel M. Bender, Andreas de Graaf, Chris Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation |
title | Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation |
title_full | Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation |
title_fullStr | Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation |
title_full_unstemmed | Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation |
title_short | Augmented Hill-Climb increases reinforcement learning efficiency for language-based de novo molecule generation |
title_sort | augmented hill-climb increases reinforcement learning efficiency for language-based de novo molecule generation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531503/ https://www.ncbi.nlm.nih.gov/pubmed/36192789 http://dx.doi.org/10.1186/s13321-022-00646-z |
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