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TaxDiff: Taxonomic-Guided Diffusion Model for Protein Sequence Generation

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arxiv 2402.17156 v1 pith:777GNKUB submitted 2024-02-27 cs.LG cs.AIq-bio.BM

classification cs.LGcs.AIq-bio.BM
keywords generationproteintaxdiffmodelssequencediffusionbiologicalcontrollable
verification ladder T0 review T1 audit T2 compute T3 formal
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Designing protein sequences with specific biological functions and structural stability is crucial in biology and chemistry. Generative models already demonstrated their capabilities for reliable protein design. However, previous models are limited to the unconditional generation of protein sequences and lack the controllable generation ability that is vital to biological tasks. In this work, we propose TaxDiff, a taxonomic-guided diffusion model for controllable protein sequence generation that combines biological species information with the generative capabilities of diffusion models to generate structurally stable proteins within the sequence space. Specifically, taxonomic control information is inserted into each layer of the transformer block to achieve fine-grained control. The combination of global and local attention ensures the sequence consistency and structural foldability of taxonomic-specific proteins. Extensive experiments demonstrate that TaxDiff can consistently achieve better performance on multiple protein sequence generation benchmarks in both taxonomic-guided controllable generation and unconditional generation. Remarkably, the sequences generated by TaxDiff even surpass those produced by direct-structure-generation models in terms of confidence based on predicted structures and require only a quarter of the time of models based on the diffusion model. The code for generating proteins and training new versions of TaxDiff is available at:https://github.com/Linzy19/TaxDiff.

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Cited by 3 Pith papers

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  3. Controllable Protein Sequence Generation with LLM Preference Optimization

    cs.AI 2025-01 conditional novelty 4.0 of 10

    CtrlProt uses multi-listwise preference optimization with Rosetta energy and structural embedding similarity to improve controllable protein sequence generation.

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