Peptides with Soft‐Aggregation Behavior Inhibit and Reverse Amyloid‐β Fibrillization
Source abstract
Abstract
Abstract Amyloid‐β fibrillization, characterized by ordered and compact peptide assembly, is a hallmark and a key therapeutic target of Alzheimer's disease. However, it is still challenging to completely inhibit or even reverse the fibrillization process. Here, it is reported an anti‐fibrillization mechanism mediated by short peptides with a novel soft‐aggregation behavior. Unlike classical peptide self‐assembly forming ordered nanostructures, several peptides derived from an analgesic peptide underwent dynamic self‐aggregation into irregular and loose nanoparticles, which is driven by strong hydrophobic interaction but not by strong hydrogen bonds. By systematically comparing different peptides, it is confirmed a direct correlation between the soft‐aggregation behavior and the anti‐fibrillization efficacy. It is further demonstrated that Ana‐5F, one of these peptides with a superior anti‐fibrillization ability, could bind with two core hydrophobic fragments in amyloid‐β and effectively inhibit their fibrillization. Consequently, Ana‐5F effectively inhibited and reversed fibrillization of full‐length amyloid‐β. In rat models, Ana‐5F cleaned up mature amyloid‐β fibrils and protected the animals from cognitive impairment and anxiety‐like behaviors. This study, for the first time, defined soft‐aggregation as a novel peptide aggregation behavior distinct from classical ordered peptide self‐assembly. It also provided a strategic approach to curing Alzheimer's disease by utilizing the soft‐aggregation mechanism to eliminate pathological amyloid‐β fibrils.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Supramolecular Self-Assembly in Materials · Alzheimer's disease research and treatments · Chemical Synthesis and Analysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Anesthesiology West China Hospital Sichuan University Chengdu 610041 China
Laboratory of Anesthesia and Critical Care Medicine National‐Local Joint Engineering Research Centre of Translational Medicine of Anesthesiology West China Hospital Sichuan University Chengdu 610041 China
Funding
Chengdu Municipal Science and Technology Program
References (51)
Show source-provided references
1. 10.1038/s41572-021-00269-y10.1038/s41572-021-00269-y ↗
2. 10.1038/s41582-024-00940-410.1038/s41582-024-00940-4 ↗
3. 10.1016/S0140-6736(20)32205-410.1016/S0140-6736(20)32205-4 ↗
4. 10.1007/s10072-022-06068-x10.1007/s10072-022-06068-x ↗
5. 10.1186/s13024-021-00456-110.1186/s13024-021-00456-1 ↗
6. 10.1038/nature2081410.1038/nature20814 ↗
7. 10.1038/s41557-020-0452-110.1038/s41557-020-0452-1 ↗
8. 10.1126/science.125555510.1126/science.1255555 ↗
9. Boopathi S. · Int. J. Mol. Sci. · 2021 · 22
10. 10.1093/brain/awad00510.1093/brain/awad005 ↗
11. 10.1016/j.brainres.2024.14901810.1016/j.brainres.2024.149018 ↗
12. 10.1016/j.cbpa.2021.05.01110.1016/j.cbpa.2021.05.011 ↗
13. 10.1021/jp111672810.1021/jp1116728 ↗
14. 10.1096/fj.05-4891fje10.1096/fj.05-4891fje ↗
15. 10.3390/biology1212153410.3390/biology12121534 ↗
16. 10.1021/acs.jpcb.4c0513510.1021/acs.jpcb.4c05135 ↗
17. 10.1021/acschemneuro.4c0003210.1021/acschemneuro.4c00032 ↗
18. 10.1002/adhm.20230465710.1002/adhm.202304657 ↗
19. 10.1016/j.jcis.2021.02.01910.1016/j.jcis.2021.02.019 ↗
20. 10.1021/acsomega.0c0097910.1021/acsomega.0c00979 ↗
21. 10.1021/acschemneuro.4c0002710.1021/acschemneuro.4c00027 ↗
22. 10.1016/j.bioorg.2024.10715910.1016/j.bioorg.2024.107159 ↗
23. 10.1039/D4MD00057A10.1039/D4MD00057A ↗
24. 10.1021/acsnano.9b0730710.1021/acsnano.9b07307 ↗
25. 10.1016/j.actbio.2017.11.02610.1016/j.actbio.2017.11.026 ↗
26. 10.1016/j.jcis.2008.07.04510.1016/j.jcis.2008.07.045 ↗
27. 10.1016/j.jcis.2009.04.01410.1016/j.jcis.2009.04.014 ↗
28. Chen Y. · Int. J. Nanomed. · 2015 · 10 · 847
29. 10.1002/psc.306210.1002/psc.3062 ↗
30. 10.3109/1040923950908514010.3109/10409239509085140 ↗
31. 10.1017/S003358350200381510.1017/S0033583502003815 ↗
32. 10.1038/s41467-023-36060-810.1038/s41467-023-36060-8 ↗
33. 10.1039/D0SC04395H10.1039/D0SC04395H ↗
34. 10.1021/acs.nanolett.5c0246310.1021/acs.nanolett.5c02463 ↗
35. 10.1038/s42004-024-01353-610.1038/s42004-024-01353-6 ↗
36. 10.1038/s41467-023-42374-410.1038/s41467-023-42374-4 ↗
37. 10.1016/j.tcb.2022.08.00610.1016/j.tcb.2022.08.006 ↗
38. T.Lazar A.Connor C. F.DeLisle V.Burger P.Tompa Nat. Rev. Drug Discovery9 Jun 2025[Epub ahead of print].
39. 10.1021/acs.analchem.7b0468610.1021/acs.analchem.7b04686 ↗
40. 10.1080/23746149.2020.177062710.1080/23746149.2020.1770627 ↗
41. 10.1002/smll.20240939210.1002/smll.202409392 ↗
42. 10.1186/s12974-019-1608-z10.1186/s12974-019-1608-z ↗
43. 10.3389/fnagi.2023.119310810.3389/fnagi.2023.1193108 ↗
44. 10.1007/s44254-023-00043-110.1007/s44254-023-00043-1 ↗
45. 10.1007/s44254-024-00078-y10.1007/s44254-024-00078-y ↗
46. 10.1016/j.actbio.2022.05.00210.1016/j.actbio.2022.05.002 ↗
47. 10.1038/nn.361810.1038/nn.3618 ↗
48. 10.1007/s12035-023-03844-410.1007/s12035-023-03844-4 ↗
49. 10.1186/s40478-022-01417-510.1186/s40478-022-01417-5 ↗
50. 10.3389/fnagi.2024.134407210.3389/fnagi.2024.1344072 ↗
51. Gage G. J. · JoVE. · 2012 · 30