mlsanityData to 7 Oct 2026

Circuit Tracing in Autoregressive Protein Language Models

arXiv 2606.16044 ↗First posted 14 Jun 2026cs.LG q-bio.QMcited by 0

Not on the map. Why?

Abstract (arXiv)

Protein language models (pLMs) can generate novel protein sequences with properties beyond those observed in nature, yet the mechanisms underlying protein generation remain poorly understood. Existing mechanistic interpretability methods based on sparse autoencoders and transcoders primarily focus on protein representation learning models and do not capture the computation required for autoregressive generation. Here, we introduce ProGenMech, a mechanistic interpretability framework for generative protein language models that extends cross-layer transcoders (CLTs) to ProGen3, a sparse Mixture-of-Experts model trained for both causal generation and span infilling. Unlike per-layer approaches, CLTs reconstruct each layer using sparse latent variables from all preceding layers, enabling faithful recovery of inter-layer generative computation. We further develop a zero-shot circuit discovery framework to identify sparse latent circuits responsible for protein generation and fitness prediction. In causal generation and zero-shot fitness estimation tasks, ProGenMech outperforms local transcoder baselines in recovering ProGen3's probability distribution and functional scoring behavior, while matching the original model's generative distribution in span infilling tasks. Moreover, the recovered circuits reveal biologically meaningful motifs and functional regions associated with conserved sequence patterns and protein fitness landscapes, establishing a foundation for interpretable and steerable protein generation.

Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 11 of its 42 references that are in the map. First posted on arXiv 14 Jun 2026.

Builds on

11 of 42 references.

References · 11

  1. 2013k-Sparse Autoencoderscited by 209
  2. 2024Transcoders Find Interpretable LLM Feature Circuitscited by 186
  3. 2026Scaling Monosemanticity: Extracting Interpretable Features from Claude 3 Sonnetcited by 175
  4. 2024InterPLM: Discovering Interpretable Features in Protein Language Models via Sparse Autoencoderscited by 64
  5. 2025Interpreting and Steering Protein Language Models through Sparse Autoencoderscited by 16
  6. 2025Towards Interpretable Protein Structure Prediction with Sparse Autoencoderscited by 12
  7. 2024On Recovering Higher-order Interactions from Protein Language Modelscited by 10
  8. 2024SHAP zero Explains Biological Sequence Models with Near-zero Marginal Cost for Future Queriescited by 4
  9. 2025Sparse Autoencoders for Low-N Protein Function Prediction and Designcited by 4
  10. 2026Protein Circuit Tracing via Cross-layer Transcoderscited by 3
  11. 2026Sparse Crosscoders for diffing MoEs and Dense modelscited by 1

Built on by

Not cited yet.

Similar, not cited

Close in wording, no citation either way

  1. 2026No Generation without Representation: Efficient Causal Protein Language Models Enable Zero-Shot Fitness Estimation
  2. 2026ProtLingo: Efficient Protein Language Modeling via Conditional Memory and Expert Routing
  3. 2024Diffusion Language Models Are Versatile Protein Learners
  4. 2024Diffusion on language model encodings for protein sequence generation
  5. 2023PoET: A generative model of protein families as sequences-of-sequences
  6. 2026Repurposing Protein Language Models for Latent Flow-Based Fitness Optimization
  7. 2024TourSynbio: A Multi-Modal Large Model and Agent Framework to Bridge Text and Protein Sequences for Protein Engineering
  8. 2025Steering Generative Models with Experimental Data for Protein Fitness Optimization