Chamaileon: Cross-Context Binder Design with Contextualized Modeling and Mixed Sampling
Hengyuan Cao, Shizhuo Cheng, Mingxuan Liu, Weicheng Huang, Yunhong Lu, CAI CHENXI, Yan Zhang, Min Zhang
ICML 2026 spotlight
Vì sao đáng đọc — góc nhìn Phở
Đa số mô hình thiết kế binder mới giả định một đích, một trạng thái. Chamaileon nới ràng buộc đó sang đa-đích và đa-trạng-thái, gần với cách protein thật hoạt động hơn. Đáng đọc nếu bạn theo dõi hướng thiết kế protein có chức năng cụ thể.
Tóm tắt (nguồn: OpenReview · © tác giả)
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.
Từ khoá
Metadata từ BioTender-max/icml2026-ai-bio (CC0-1.0). Phở không lưu trữ bản PDF; link trỏ về nguồn gốc.
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