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UniMoMo: Unified Generative Modeling of 3D Molecules for De Novo Binder Design

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arxiv 2503.19300 v3 pith:EHZ33FEB submitted 2025-03-25 cs.LG q-bio.BM

classification cs.LGq-bio.BM
keywords moleculesunimomogenerativemodelmolecularunifiedantibodiesblocks
verification ladder T0 review T1 audit T2 compute T3 formal
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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.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. MODA: A Unified 3D Diffusion Framework for Multi-Task Target-Aware Molecular Generation

    q-bio.BM 2025-07 conditional novelty 6.0 of 10

    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.

  2. Reimagining Target-Aware Molecular Generation through Retrieval-Enhanced Aligned Diffusion

    q-bio.BM 2025-06 conditional novelty 5.0 of 10

    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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