Joseph M. Paggi

Christopher Fifty, Joseph M. Paggi, Ehsan Amid et al.

Few-shot learning is a promising approach to molecular property prediction as supervised data is often very limited. However, many important molecular properties depend on complex molecular characteristics -- such as the various 3D geometries a molecule may adopt or the types of chemical interactions it can form -- that are not explicitly encoded in the feature space and must be approximated from low amounts of data. Learning these characteristics can be difficult, especially for few-shot learning algorithms that are designed for fast adaptation to new tasks. In this work, we develop molecular embeddings that encode complex molecular characteristics to improve the performance of few-shot molecular property prediction. Our approach leverages large amounts of synthetic data, namely the results of molecular docking calculations, and a multi-task learning paradigm to structure the embedding space. On multiple molecular property prediction benchmarks, training from the embedding space substantially improves Multi-Task, MAML, and Prototypical Network few-shot learning performance. Our code is available at https://github.com/cfifty/IGNITE.

Patricia Suriana, Joseph M. Paggi, Ron O. Dror

Most widely used ligand docking methods assume a rigid protein structure. This leads to problems when the structure of the target protein deforms upon ligand binding. In particular, the ligand's true binding pose is often scored very unfavorably due to apparent clashes between ligand and protein atoms, which lead to extremely high values of the calculated van der Waals energy term. Traditionally, this problem has been addressed by explicitly searching for receptor conformations to account for the flexibility of the receptor in ligand binding. Here we present a deep learning model trained to take receptor flexibility into account implicitly when predicting van der Waals energy. We show that incorporating this machine-learned energy term into a state-of-the-art physics-based scoring function improves small molecule ligand pose prediction results in cases with substantial protein deformation, without degrading performance in cases with minimal protein deformation. This work demonstrates the feasibility of learning effects of protein flexibility on ligand binding without explicitly modeling changes in protein structure.