Background: Single-target Alzheimer’s disease (AD) therapies have repeatedly failed to modify disease progression, highlighting a critical mismatch between multifactorial pathology and reductionist pharmacology. Methods: We developed a representation learning framework using Knowledge-guided Pre-trained Graph Transformers (KPGT) to enable rational multi-target drug discovery, analyzing 2446 molecules across APP, PSEN1, and VCP. Results: KPGT captured target-specific mechanistic signatures with 99.35% classification accuracy. Geometric midpoint analysis identified 15 bridging candidates with mean pIC50 8.09. We discovered two orthogonal molecular feature signatures, structural features driving multi-target breadth versus chemical features determining single-target potency, with zero descriptor overlap. Chemical orthogonality (d = 3.86) outperformed functional similarity for predicting synergistic pairs, with 95% overlap between multi-target molecules and synergistic combinations. Conclusions: This framework operationalizes systems-level AD drug discovery through interpretable representation learning.
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Zhou et al. (Tue,) studied this question.
synapsesocial.com/papers/69d894ec6c1944d70ce05d08 — DOI: https://doi.org/10.3390/jdad3020019
Junyu Zhou
Twitter (United States)
Mingxi Chen
Peking University
Journal of dementia and Alzheimer's disease
Peking University
Guangdong Technion-Israel Institute of Technology
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