ToursynClaw: Superintelligent Agents for Protein Design

Collaborative AI agent for protein scientists that leverages natural-language interaction to complete the entire workflow - from target analysis to wet-lab experiments - in one place.

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ToursynClaw: Scientific Superintelligence Focused on Biopharma R&D

ToursynClaw is our proprietary AI protein design platform integrating 20+ specialized models across target analysis, structure prediction, molecular generation, performance evaluation, and candidate selection to accelerate innovative biologic discovery and development.

ToursynClaw dry and wet lab workflow

Scientific Superintelligence Agents

Its core technology centers on AI-driven protein design, and it has built multiple proprietary platforms and models at world-leading levels with superior integrated performance.

ToursynClaw agent workspace on a laptop

Proprietary Closed - Source Protein Design Model

Dry-Wet Integrated Superintelligence lab

Automated wet-lab and data flywheel layers

Integrated Superintelligent Technology

Proprietary closed-source protein design models with performance on par with SOTA open-source models. Ascend C operator optimization and hardware-software co-design deliver superior inference speed.

AI Scientist Agent

Autonomously designs experiments, proposes AI solutions, and automates data processing and model training. Interacts independently with wet-lab agents and updates iteratively every 3 days.

Antibody Testing Agent

Fully automatically builds plasmids and proteins from amino-acid sequences recommended by the AI platform and returns high-throughput test results in 11 days.

De novo Design

Indication: CLDN18.2-Positive Solid Tumors

CLDN18.2 is a clinically validated therapeutic target primarily associated with gastric cancer and gastroesophageal junction adenocarcinoma, with potential applications in pancreatic cancer and other CLDN18.2-positive solid tumors.

Claudin-18.2

1
Month Timeline
30
Designed Antibodies
2
Functional Hits
8nM
Best Binding Affinity
CLDN18.2 protein structure