AMix-2: Establishing Protein as a Native Modality in Large Language Models
- URL: http://arxiv.org/abs/2605.30963v1
- Date: Fri, 29 May 2026 07:58:08 GMT
- Title: AMix-2: Establishing Protein as a Native Modality in Large Language Models
- Abstract summary: We present AMix-2, a protein-text foundation model that establishes protein as a native modality in large language models (LLMs)<n>AMix-2 is built upon two key ideas: (1) a unified protein-text formulation that embeds natural language and protein sequence in a shared token space; and (2) a block-wise diffusion language modeling backbone.<n>We introduce ProteinArena, a comprehensive benchmark with time-aware and homology-aware protocols across various understanding and design tasks.
- Score: 88.00237394496698
- License: http://creativecommons.org/licenses/by-nc-sa/4.0/
- Abstract: We present AMix-2, a protein-text foundation model that establishes protein as a native modality in large language models (LLMs), unifying protein understanding and sequence design within a single foundation model. AMix-2 is built upon two key ideas: (1) a unified protein-text formulation that embeds natural language and protein sequence in a shared token space, enabling one model to perform biological reasoning and conditional design instead of separate downstream task-specialized models; and (2) a block-wise diffusion language modeling backbone that combines causal generation across blocks with bidirectional context and iterative refinement within blocks. This scheme better matches the intrinsic nature of proteins than a strict left-to-right factorization. To evaluate protein foundation models under realistic generalization settings, we further introduce ProteinArena, a comprehensive benchmark with time-aware and homology-aware protocols across various understanding and design tasks, and with baselines covering classical bioinformatics tools, protein-specialized models and LLMs. On ProteinArena, AMix-2 outperforms frontier LLMs and demonstrates competitive performance to task-specific protein models. Controlled experiments further show that the diffusion-based paradigm generally surpasses its autoregressive counterpart, highlighting the advantage of flexible generation order for protein sequences. We release both AMix-2 and ProteinArena to facilitate open research in protein foundation models.
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