Large property models: a new generative machine-learning formulation for molecules
Generative models for the inverse design of molecules with particular properties have been heavily hyped, but have yet to demonstrate significant gains over machine-learning-augmented expert intuition. A major challenge of such models is their limited accuracy in predicting molecules with targeted properties in the data-scarce regime, which is the regime typical of the prized outliers that it is hoped inverse models will discover. For example, activity data for a drug target or stability data for a material may only number in the tens to hundreds of samples, which is insufficient to learn an accurate and reasonably general property-to-structure inverse mapping from scratch. We've hypothesized that the property-to-structure mapping becomes unique when a sufficient number of properties are supplied to the models during training. This hypothesis has several important corollaries if true. It would imply that data-scarce properties can be completely determined using a set of more accessible molecular properties. It would also imply that a generative model trained on multiple properties would exhibit an accuracy phase transition after achieving a sufficient size-a process analogous to what has been observed in the context of large language models. To interrogate these behaviors, we have built the first transformers trained on the property-to-molecular-graph task, which we dub "large property models" (LPMs). A key ingredient is supplementing these models during training with relatively basic but abundant chemical property data. The motivation for the large-property-model paradigm, the model architectures, and case studies are presented here.
Authors
- Brett Matthew Savoie (ORCID: https://orcid.org/0000-0002-7039-4039)
- Veerupaksh Singla (ORCID: https://orcid.org/0000-0001-6300-2167)
- Hsuan‐Hao Hsu
- Tianfan Jin
Institutions
- University of Notre Dame (US)
- Purdue University West Lafayette (US)
Publication Details
- Journal
- Faraday Discussions
- Published
- 2024-09-27
- DOI
- https://doi.org/10.1039/d4fd00113c
- Citations
- 5
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.81
Funders
- National Science Foundation
- Division of Chemical, Bioengineering, Environmental, and Transport Systems