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Molecular glue degraders: Rational design, specificity engineering, and advanced delivery
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Acta Pharmaceutica Sinica B | 2026, 16(7) : 4261 - 4284
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Acta Pharmaceutica Sinica B | 2026, 16(7): 4261-4284
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Molecular glue degraders: Rational design, specificity engineering, and advanced delivery
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Lieen Ma1, Ning Wang2, Jingjing Zhu3, Lingjie Wu1, Shan He1,4, Bin Zhang1
Affiliations
    1 School of Pharmacy, Health Science Center, Ningbo University, Ningbo 315211, China;
    2 Institute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China;
    3 Research & Development Center, HEALTH BioMed C15., Lt4., Ningbo 315040, China;
    4 Ningbo Institute of Marine Medicine, Peking University, Ningbo 315832, China
doi: 10.1016/j.apsb.2026.02.020
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Molecular glue degraders (MGDs) have emerged as a transformative modality in the field of targeted protein degradation (TPD), enabling the selective elimination of disease-relevant proteins, including those traditionally considered undruggable. Unlike bifunctional proteolysis-targeting chimeras (PROTACs), MGDs operate through monovalent architectures that induce protein-protein interactions (PPIs) between E3 ligases and neosubstrates, offering advantages in chemical simplicity, cell permeability, and target scope. However, MGD discovery remains serendipitously, and a translational framework that links rational design to predictable selectivity and tissue exposure is still lacking. In this review, we present an integrated framework for advancing next-generation MGDs through three critical dimensions: rational design, specificity optimization, and delivery systems. First, we examined cutting-edge strategies in MGD design, including covalent handle-based reprogramming, PPI-driven stabilization, and multi-site, multi-functional constructs. Second, we explored structure-guided engineering and chemoinformatic models, such as cereblon degron motifs, zone-based design and multiparameter optimization, to improve neosubstrate selectivity while minimizing off-target liabilities. Third, we summarized delivery platforms, including antibody-drug conjugates, nanoparticle-enabled systems, and folate-mediated targeting, which are primarily intended to improve tissue selectivity and targeted distribution, thereby promoting local tissue accumulation. Finally, we discussed emerging opportunities at the intersection of artificial intelligence, structural biology, and systems pharmacology for accelerating MGD discovery and clinical translation. Collectively, these interdisciplinary insights underscore the therapeutic promise of MGDs and lay the groundwork for their next-generation evolution in precision medicine.
Molecular glue degraders  /  Targeted protein degradation  /  Rational design  /  E3 ligases  /  Specificity engineering  /  Drug delivering systems
Lieen Ma, Ning Wang, Jingjing Zhu, Lingjie Wu, Shan He, Bin Zhang. Molecular glue degraders: Rational design, specificity engineering, and advanced delivery[J]. Acta Pharmaceutica Sinica B, 2026 , 16 (7) : 4261 -4284 . DOI: 10.1016/j.apsb.2026.02.020
Year 2026 volume 16 Issue 7
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doi: 10.1016/j.apsb.2026.02.020
  • Receive Date:2025-11-28
  • Online Date:2026-09-17
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  • Received:2025-11-28
  • Revised:2026-02-04
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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