Fight Aβ Aggregation with Molecular Aggregates

Abstract Alzheimer's disease (AD) is the most common form of neurodegenerative disease. Aggregation of amyloid‐β peptides (Aβ), a characteristic molecular event of AD, may produce neurotoxic aggregates, notably oligomers that can induce a series of pathogenic change, finally leading to AD. Suppression of Aβ aggregates‐induced neurotoxicity via intervention of Aβ aggregation or removal of toxic aggregates are considered as an effective approach for AD treatment. Notably, molecular aggregates formed by assembly of organic molecules have demonstrated promising potential to fight Aβ aggregation due to their advantages, such as high binding affinity, blood‐brain barrier permeability, as well as synergistic effect between multiple functionalities, resulting from their unique physicochemical properties in the aggregate state. This review focuses on the recent progress of molecular aggregates for fighting Aβ aggregation in terms of inhibition of Aβ aggregation, redirection of Aβ aggregation into non‐toxic aggregates, disassembly of Aβ aggregates, and clearance of Aβ aggregates. Representative examples of the molecular aggregates are categorized by assembly block and manner. Their structural design, working mechanism, and potential of anti‐AD are highlighted. Finally, the perspectives and challenges of Aβ aggregation‐oriented molecular aggregates for future research are also proposed.

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Publication Details

Journal
Macromolecular Chemistry and Physics
Published
2025-03-05
DOI
https://doi.org/10.1002/macp.202400531
Citations
2
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
1.61

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article

Fight Aβ Aggregation with Molecular Aggregates

Ming Hu, Cheng Wang, Xiaohui Wang, Dingxin Zhang
2 citations
Macromolecular Chemistry and Physics
Protein Structure and Dynamics
1.61
article

Fight Aβ Aggregation with Molecular Aggregates

Ming Hu, Cheng Wang, Xiaohui Wang, Dingxin Zhang
article en
2 citations

Abstract

Abstract Alzheimer's disease (AD) is the most common form of neurodegenerative disease. Aggregation of amyloid‐β peptides (Aβ), a characteristic molecular event of AD, may produce neurotoxic aggregates, notably oligomers that can induce a series of pathogenic change, finally leading to AD. Suppression of Aβ aggregates‐induced neurotoxicity via intervention of Aβ aggregation or removal of toxic aggregates are considered as an effective approach for AD treatment. Notably, molecular aggregates formed by assembly of organic molecules have demonstrated promising potential to fight Aβ aggregation due to their advantages, such as high binding affinity, blood‐brain barrier permeability, as well as synergistic effect between multiple functionalities, resulting from their unique physicochemical properties in the aggregate state. This review focuses on the recent progress of molecular aggregates for fighting Aβ aggregation in terms of inhibition of Aβ aggregation, redirection of Aβ aggregation into non‐toxic aggregates, disassembly of Aβ aggregates, and clearance of Aβ aggregates. Representative examples of the molecular aggregates are categorized by assembly block and manner. Their structural design, working mechanism, and potential of anti‐AD are highlighted. Finally, the perspectives and challenges of Aβ aggregation‐oriented molecular aggregates for future research are also proposed.

Macromolecular Chemistry and PhysicsVol. 226(11)
Nanjing Tech University (CN)
National Natural Science Foundation of China, Natural Science Research of Jiangsu Higher Education Institutions of China
Openalex Percentile: Top 19%
Protein Structure and Dynamics
1.61
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Fight Aβ Aggregation with Molecular Aggregates — Ming Hu, Cheng Wang, et al. · Macromolecular Chemistry and Physics (2025) | TGRS Research Map | TGRS