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March 10, 2026Briefings in Bioinformatics1 citationsOpen Access

De novo functional protein sequence generation: overcoming data scarcity through regeneration and large language models

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CRChenyu RenHong Kong Polytechnic UniversityDHDaihai HeHong Kong Polytechnic UniversityJHJian HuangShanghai University

Key Points

  • The aim is to generate functional protein sequences effectively despite limited data availability.
  • Developed a hierarchical model named ProteinRG for protein sequence generation.
  • Used existing large protein sequence models to generate representations of protein sequences.
  • Evaluated generated sequences through multiple sequence alignment, t-SNE distribution analysis, and 3D structure prediction.
  • Generated protein sequences show high similarity to original sequences.
  • Maintained consistency with the intended functional roles of proteins.
  • Outperformed other generative models in protein sequence generation.

Abstract

Abstract Proteins are essential components of all living organisms and play a critical role in cellular survival. They have a broad range of applications, from clinical treatments to material engineering. This versatility has spurred the development of protein design, with amino acid sequence design being a crucial step in the process. Recent advancements in deep generative models have shown promise for protein sequence design. However, the scarcity of functional protein sequence data for certain types can hinder the training of these models, which often require large datasets. To address this challenge, we propose a hierarchical model named ProteinRG that can generate functional protein sequences using relatively small datasets. ProteinRG begins by generating a representation of a protein sequence, leveraging existing large protein sequence models, before producing a functional protein sequence. We have tested our model on various functional protein sequences and evaluated the results from three perspectives: multiple sequence alignment, t-SNE distribution analysis, and 3D structure prediction. The findings indicate that our generated protein sequences maintain both similarity to the original sequences and consistency with the desired functions. Moreover, our model demonstrates superior performance compared twith other generative models for protein sequence generation.

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Cite This Study

Ren et al. (2026) studied this question.

synapsesocial.com/papers/69af959570916d39fea4d562https://doi.org/10.1093/bib/bbag095
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