DiffDTM: A conditional structure-free framework for bioactive molecules generation targeted for dual proteins

• URL: http://arxiv.org/abs/2306.13957v1
• Date: Sat, 24 Jun 2023 13:08:55 GMT
• Title: DiffDTM: A conditional structure-free framework for bioactive molecules generation targeted for dual proteins
• Authors: Lei Huang, Zheng Yuan, Huihui Yan, Rong Sheng, Linjing Liu, Fuzhou Wang, Weidun Xie, Nanjun Chen, Fei Huang, Songfang Huang, Ka-Chun Wong, Yaoyun Zhang
• Abstract summary: DiffDTM is a conditional structure-free deep generative model based on a diffusion model for dual targets based molecule generation. We have conducted comprehensive multi-view experiments to demonstrate that DiffDTM can generate drug-like, synthesis-accessible, novel, and high-binding affinity molecules. The experimental results indicate that DiffDTM can be easily plugged into unseen dual targets to generate bioactive molecules.
• Score: 35.72694124335747
• License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
• Abstract: Advances in deep generative models shed light on de novo molecule generation with desired properties. However, molecule generation targeted for dual protein targets still faces formidable challenges including protein 3D structure data requisition for model training, auto-regressive sampling, and model generalization for unseen targets. Here, we proposed DiffDTM, a novel conditional structure-free deep generative model based on a diffusion model for dual targets based molecule generation to address the above issues. Specifically, DiffDTM receives protein sequences and molecular graphs as inputs instead of protein and molecular conformations and incorporates an information fusion module to achieve conditional generation in a one-shot manner. We have conducted comprehensive multi-view experiments to demonstrate that DiffDTM can generate drug-like, synthesis-accessible, novel, and high-binding affinity molecules targeting specific dual proteins, outperforming the state-of-the-art (SOTA) models in terms of multiple evaluation metrics. Furthermore, we utilized DiffDTM to generate molecules towards dopamine receptor D2 and 5-hydroxytryptamine receptor 1A as new antipsychotics. The experimental results indicate that DiffDTM can be easily plugged into unseen dual targets to generate bioactive molecules, addressing the issues of requiring insufficient active molecule data for training as well as the need to retrain when encountering new targets.

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