Towards Unified Latent Space for 3D Molecular Latent Diffusion Modeling
Abstract
3D molecule generation is crucial for drug discovery and material science, requiring models to process complex multi-modalities, including atom types, chemical bonds, and 3D coordinates. A key challenge is integrating these modalities of different shapes while maintaining SE(3) equivariance for 3D coordinates. To achieve this, existing approaches typically maintain separate latent spaces for invariant and equivariant modalities, reducing efficiency in both training and sampling. In this work, we propose Unified Variational Auto-Encoder for 3D Molecular Latent Diffusion Modeling (UAE-3D), a multi-modal VAE that compresses 3D molecules into latent sequences from a unified latent space, while maintaining near-zero reconstruction error. This unified latent space eliminates the complexities of handling multi-modality and equivariance when performing latent diffusion modeling. We demonstrate this by employing the Diffusion Transformer--a general-purpose diffusion model without any molecular inductive bias--for latent generation. Extensive experiments on GEOM-Drugs and QM9 datasets demonstrate that our method significantly establishes new benchmarks in both de novo and conditional 3D molecule generation, achieving leading efficiency and quality.
Community
UAE-3D is a recent effort on addressing the important challenge in 3D molecule generation—integrating heterogeneous modalities (atom types, chemical bonds, and 3D coordinates) while preserving the SE(3) equivariance critical for spatial consistency. Previous methods often rely on separate latent spaces for invariant and equivariant information, which complicates both training and sampling. In contrast, UAE-3D, a multi-modal variational autoencoder that compresses 3D molecular data into a single, unified latent space with near-zero reconstruction error. This design removes the complexities inherent in handling multi-modality and equivariance in latent diffusion modeling.
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