AI
Learning Latent Protein Languages for Autoregressive Generation
Publication: Hugging Face Daily Papers
Author: Not available in collected metadata
Source published: 01/10/2026, 20:00:00 UTC
Briefing created: 22/10/2026, 14:39:23 UTC
Based on a feed excerpt; full article content has not been acquired. Source evidence retrieved 06/10/2026, 17:18:24 UTC.
Briefings
This study introduces two learned latent protein languages, PLL and SLL, designed to improve autoregressive generation for protein sequences and structures. PLL maps amino acid residues to a 4,096-state alphabet using a frozen ESM-2 encoder, while SLL adapts GCP-VQVAE Lite with sequence supervision. Pretraining on these languages yields PLLM and SLLM, which outperform standard amino acid models in compute-scaling efficiency and reduce entropy below 1.5-bit thresholds by 54% during generation. For sequence-to-structure prediction, SLLM reduces validation perplexity by 34% compared to the original tokenizer, and long proteins are generated 1,000 times faster than MSA-based AlphaFold2.
Key points
- PLL maps amino acid residues to a 4,096-state contextual alphabet using a frozen ESM-2 encoder, with one token per residue.
- SLL adapts GCP-VQVAE Lite with auxiliary sequence and confidence supervision to retain decoding to backbone coordinates.
Context
Autoregressive transformers currently struggle with protein sequence and structure generation. This research addresses this by introducing learned latent protein languages that encode residue identities without explicit contextual semantics, addressing a key limitation in current generative models.
Limitations
Results are based on internal measurements and pretraining data; long protein performance is approximate. No additional background context is supplied beyond the provided evidence.
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