Yiran Tao

Yiran Tao, Jehan Yang, Dan Ding et al. · cmu

Teleoperating high degrees-of-freedom (DoF) robotic manipulators via low-DoF controllers like joysticks often requires frequent switching between control modes, where each mode maps controller movements to specific robot actions. Manually performing this frequent switching can make teleoperation cumbersome and inefficient. On the other hand, existing automatic mode-switching solutions, such as heuristic-based or learning-based methods, are often task-specific and lack generalizability. In this paper, we introduce LLM-Driven Automatic Mode Switching (LAMS), a novel approach that leverages Large Language Models (LLMs) to automatically switch control modes based on task context. Unlike existing methods, LAMS requires no prior task demonstrations and incrementally improves by integrating user-generated mode-switching examples. We validate LAMS through an ablation study and a user study with 10 participants on complex, long-horizon tasks, demonstrating that LAMS effectively reduces manual mode switches, is preferred over alternative methods, and improves performance over time. The project website with supplementary materials is at https://lams-assistance.github.io/.

Hanqi Feng, Peng Qiu, Mengchun Zhang et al.

Recent advances in diffusion models have shown remarkable potential for antibody design, yet existing approaches apply uniform generation strategies that cannot adapt to each antigen's unique requirements. Inspired by B cell affinity maturation, where antibodies evolve through multi-objective optimization balancing affinity, stability, and self-avoidance, we propose the first biologically-motivated framework that leverages physics-based domain knowledge within an online meta-learning system. Our method employs multiple specialized experts (van der Waals, molecular recognition, energy balance, and interface geometry) whose parameters evolve during generation based on iterative feedback, mimicking natural antibody refinement cycles. Instead of fixed protocols, this adaptive guidance discovers personalized optimization strategies for each target. Our experiments demonstrate that this approach: (1) discovers optimal SE(3)-equivariant guidance strategies for different antigen classes without pre-training, preserving molecular symmetries throughout optimization; (2) significantly enhances hotspot coverage and interface quality through target-specific adaptation, achieving balanced multi-objective optimization characteristic of therapeutic antibodies; (3) establishes a paradigm for iterative refinement where each antibody-antigen system learns its unique optimization profile through online evaluation; (4) generalizes effectively across diverse design challenges, from small epitopes to large protein interfaces, enabling precision-focused campaigns for individual targets.