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<p>Functional nucleic acids (FNAs) are essential elements for designing advanced molecular tools, yet their de novo design faces challenges due to the vast sequence space and inefficiency of experimental screening methods. Nucleic acid large language models (NA-LLMs) offer new opportunities for FNA design, but their generative capability remains underexplored. Here we introduce InstructNA, a framework leveraging NA-LLMs and high-throughput systematic evolution of ligands by exponential enrichment (HT-SELEX) to guide de novo design of FNAs without relying on structural information. InstructNA encodes semantically rich FNA representations and robustly decodes FNA sequences, enabling the generation of various types of FNA such as transcription factor-binding DNA and protein-binding aptamers with enhanced functionality and high sequence diversity. Compared with the traditional HT-SELEX, InstructNA generates 100% and 200% more strong aptamer binders for two protein targets, with a sequence similarity to the original HT-SELEX aptamers as low as 38%. These results underscore the efficacy and robustness of InstructNA, demonstrating its potential for FNA design.</p>

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De novo design of functional nucleic acids of aptamers

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月11日

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  • Zhiming Zhang,
  • Meng Jiang,
  • Axin He,
  • Youyuan Zhu,
  • Ercheng Wang,
  • Liqi Wan,
  • Jiezhong Qiu,
  • Pei Guo,
  • Guangyong Chen,
  • Da Han

摘要

Functional nucleic acids (FNAs) are essential elements for designing advanced molecular tools, yet their de novo design faces challenges due to the vast sequence space and inefficiency of experimental screening methods. Nucleic acid large language models (NA-LLMs) offer new opportunities for FNA design, but their generative capability remains underexplored. Here we introduce InstructNA, a framework leveraging NA-LLMs and high-throughput systematic evolution of ligands by exponential enrichment (HT-SELEX) to guide de novo design of FNAs without relying on structural information. InstructNA encodes semantically rich FNA representations and robustly decodes FNA sequences, enabling the generation of various types of FNA such as transcription factor-binding DNA and protein-binding aptamers with enhanced functionality and high sequence diversity. Compared with the traditional HT-SELEX, InstructNA generates 100% and 200% more strong aptamer binders for two protein targets, with a sequence similarity to the original HT-SELEX aptamers as low as 38%. These results underscore the efficacy and robustness of InstructNA, demonstrating its potential for FNA design.