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August 14, 2026Smart Molecules0 citationsOpen Access

Artificial intelligence empowers targeted protein degradation: Core technological innovations, multi‐scenario applications, and translational prospects

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SQShuanglin QinRPRui PengGZGuangshuai Zhang

Key Points

  • To review the core technological innovations, practical applications, and translational prospects of artificial intelligence in advancing targeted protein degradation.
  • Systematically surveyed AI-driven computational methods applied across major TPD modalities, including PROTACs, molecular glues, and LYTACs.
  • Assessed predictive modeling architectures used for ternary complex formation, linker optimization, E3 ligase ligand screening, and ADMET profiling.
  • Synthesized AI advancements enabling rational linker design, automated molecular glue discovery, and enhanced prediction of degradation efficiency.
  • Identified critical translational bottlenecks, such as a lack of standardized datasets and model opacity, while proposing solutions like explainable AI and multi-omics integration.

Abstract

Abstract Targeted protein degradation (TPD) has emerged as a transformative therapeutic strategy that offers unprecedented opportunities to eliminate traditionally “undruggable” proteins that have posed significant challenges in traditional drug development. Current TPD approaches, including proteolysis‐targeting chimeras (PROTACs), molecular glues, and lysosome‐targeting chimeras (LYTACs), encounter several limitations. These include the complexity of forming stable ternary complexes, suboptimal design of linkers, a limited repertoire of E3 ligases, and inadequate pharmacokinetic properties. Artificial intelligence (AI) has rapidly become essential in addressing these challenges, revolutionizing the TPD drug discovery process through data‐driven insights and predictive modeling. This review systematically explores AI applications in TPD development, covering the prediction and design of stable ternary complexes, rational optimization of linkers, high‐throughput screening for E3 ligase ligands, and accurate predictions of degradation efficiency and ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity) properties. Additionally, this review underscores AI's pioneering role in discovering molecular glues, from target identification to activity prediction, and discusses the AI‐driven optimization of emerging TPD modalities, such as LYTACs and PROTAC/IMiD bifunctional molecules. Despite significant progress, several critical challenges remain, such as the absence of standardized datasets, the static modeling of dynamic biological systems, and the opaque nature of advanced AI architectures. Future research should concentrate on integrating multi‐omics data to improve model training, developing dynamic and mechanistic AI frameworks, advancing explainable AI (XAI) to enhance mechanistic interpretability, and encouraging transdisciplinary collaboration to expedite clinical translation. By integrating AI with structural biology, pharmacology, and experimental validation, TPD technologies hold the potential to expand the druggable proteome and provide novel therapeutic solutions for cancer, neurological disorders, and other persistent diseases.

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Cite This Study

Qin et al. (2026) studied this question.

synapsesocial.com/papers/6a7ec764b70b84ec8b913b56https://doi.org/10.1002/smo2.70089
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  4. 4PROTACs in Targeted Protein Degradation: Advances in Development and AI-Enhanced Drug Discovery2026 · 3 citations
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