Chamaileon: Cross-Context Binder Design with Contextualized Modeling and Mixed Sampling

摘要

The rapid evolution of generative models has unlocked new potentials in protein binder design, a pivotal task in structural biology, by facilitating end-to-end generation via joint sequence-structure modeling or hallucination. However, existing approaches are predominantly implemented under a single-target, single-state assumption, limiting their ability to model multi-target or multi-state interactions required for advanced function-oriented protein design. Here, we introduce Chamaileon, which unifies multi-target and multi-state binder design by formulating the problem as cross-context binding landscape modeling. The framework is underpinned by a training paradigm termed \textit{In-Context Complex Co-Design (I3CD)} for context-aware sequence-structure co-modeling. During inference, we employ \textit{Mixture-of-Paths Sampling (MoPS)}, a scalable strategy that optimizes a single sequence across contexts while alleviating the scarcity of high-quality multi-conformational paired data. Extensive evaluation on our newly constructed benchmark, \textit{CROSS}, demonstrates that Chamaileon effectively generates sequences adaptable to diverse conformational landscapes and multi-target requirements.