Self-evolving AI agents for protein discovery and directed evolution

Scientific research proceeds through iterative cycles of hypothesis generation, experiment design, execution, and revision. AI agents can automate parts of this process, but existing approaches typically follow a single research trajectory or coordinate through a central planner with fixed objectives. As a result, they struggle to sustain parallel exploration, adapt as experimental evidence changes, or preserve knowledge of failed directions over long-running experiments. We introduce AutoScientists, a decentralized team of AI agents for long-running computational scientific experimentation. Agents interpret a shared experimental state, self-organize into teams around promising hypotheses, critique proposals before using experimental compute, and share successes and failures to reduce redundant exploration. Under matched experimental budgets, AutoScientists improves over prior AI agents across biomedical machine learning, language-model training optimization, and protein fitness prediction. On BioML-Bench, spanning biomedical imaging, protein engineering, single-cell omics, and drug discovery, AutoScientists achieves a mean leaderboard percentile of 74.4% across 24 tasks, improving over the strongest AI agent by +8.33%. On GPT training optimization, AutoScientists reaches a target validation bits-per-byte 1.9x faster than Autoresearch and continues discovering improvements from a starting champion where the single-agent approach finds none (7 vs. 0 accepted improvements). On ProteinGym fitness prediction, AutoScientists discovers a method for ACE2-Spike binding that improves over the current state-of-the-art model by +12.5% in Spearman correlation. Applied without modification across all 217 ProteinGym assays, the same method improves over the prior state of the art by +6.5% (Spearman correlation).

AI for scientific discovery is entering an agentic era, where protein-engineering systems are expected to prioritize future wet-lab experiments rather than merely fit static measurements. We introduce TadA-Bench, a million-variant wet-lab replay benchmark from 31 TadA directed-evolution rounds for future-round discovery toward agentic protein engineering. TadA-Bench preserves the campaign chronology and defines a fixed-data replay task: given earlier experimental rounds, models rank variants that appear only in later rounds. It provides aligned DNA, RNA, and protein views, and uses Seq2Graph, a graph-based label-unification pipeline, to reconcile noisy enrichment measurements into consistent cross-round activity labels. Random-split controls show strong interpolation, but future-round ranking and finite-budget candidate selection are much weaker. Controlled analyses suggest that evolutionary coverage is more informative than local data density, positioning TadA-Bench as a reproducible wet-lab replay substrate for future-round discovery toward agentic protein engineering; the data and code are released on Hugging Face and GitHub.

What happens when you teach an LLM-based agent the scientific method? Motivation: Scientific discovery emerges from cycles of hypothesis, implementation, empirical testing, and feedback. Can this process be automated? We approach automated algorithm design through the lens of the scientific method, where an LLM-based agent goes through each step of the process in an ordered, iterative fashion. Results: We present The Little Scientist, a framework in which a "Scientist agent" works inside an evaluation environment that benchmarks its code and returns structured per-instance diagnostics. When the Scientist plateaus at a local optimum, a "Kuhn agent" injects a paradigm-shifting conjecture paired with a cross-disciplinary inspiration, forcing exploration of a different region of the LLM's latent space. We demonstrate the framework on two problems that require fundamentally different modes of discovery. For protein fitness prediction, the Scientist discovered Delta V, an ensemble calibration strategy that ranks first on the ProteinGym DMS Substitutions Zero-Shot leaderboard across all five official evaluation metrics, exceeding the #2 model (VenusREM) by +0.033 mean Spearman correlation across 217 DMS assays. For DNA motif discovery, the Scientist wrote an algorithm from scratch--DALE (Dual-seed Algorithm for Latent Enumeration)--that outperforms STREME (the default in the MEME Suite) across 132 ENCODE transcription factors (mean AUROC 0.842 vs. 0.803, Wilcoxon p < 10^{-6}) while running 11x faster. This demonstrates that the framework can produce genuinely novel algorithms, not just optimize existing components. Together, these results show that an LLM agent stepping through the scientific method can discover both new algorithms and new ensemble strategies that outperform prior solutions. The entire research program consumed 704M tokens on a single virtual machine with no GPUs