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UniMoMo: Unified Generative Modeling of 3D Molecules for De Novo Binder Design
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The design of target-specific molecules such as small molecules, peptides, and antibodies is vital for biological research and drug discovery. Existing generative methods are restricted to single-domain molecules, failing to address versatile therapeutic needs or utilize cross-domain transferability to enhance model performance. In this paper, we introduce Unified generative Modeling of 3D Molecules (UniMoMo), the first framework capable of designing binders of multiple molecular domains using a single model. In particular, UniMoMo unifies the representations of different molecules as graphs of blocks, where each block corresponds to either a standard amino acid or a molecular fragment. Subsequently, UniMoMo utilizes a geometric latent diffusion model for 3D molecular generation, featuring an iterative full-atom autoencoder to compress blocks into latent space points, followed by an E(3)-equivariant diffusion process. Extensive benchmarks across peptides, antibodies, and small molecules demonstrate the superiority of our unified framework over existing domain-specific models, highlighting the benefits of multi-domain training.
Forward citations
Cited by 2 Pith papers
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MODA: A Unified 3D Diffusion Framework for Multi-Task Target-Aware Molecular Generation
A single masked-diffusion model trained jointly on four molecular-editing tasks outperforms or matches task-specific diffusion baselines across docking, chemical property, and geometry metrics.
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Reimagining Target-Aware Molecular Generation through Retrieval-Enhanced Aligned Diffusion
READ couples contrastively aligned latent diffusion with pocket-similarity retrieval to generate 3D ligands, reporting Rank 1 on CBGBench and lower Vina energies than native ligands.
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