Boosting the Photodynamic Degradation of Islet Amyloid Polypeptide Aggregates Via a “Bait-Hook-Devastate” Strategy
Source abstract
Abstract
Photosensitizers that can generate reactive oxygen species (ROS) upon irradiation have emerged as promising agents for photodynamic degradation of toxic amyloid aggregates that are linked to many amyloidogenic diseases. However, due to the ultrastable β-sheet structure in amyloid aggregates and inefficient utilization of the generated ROS, it usually requires high stoichiometric concentration of the photosensitizer and/or intensive light irradiation to fully dissociate aggregates. In this work, we have developed a "bait-hook-devastate" strategy to boost the efficiency of the photodynamic degradation of amyloid aggregates. This strategy employs anionic polyacrylic acid as a bait to accumulate cationic human islet amyloid polypeptide (IAPP) aggregates and positively charged photosensitizer TPCI in a confined area through electronic interactions. Multiple characterization studies proved that the utilization rate of ROS generated by TPCI was remarkably improved via this strategy, which amplified the ability of TPCI to dissociate IAPP aggregates. Rapid and complete degradation of IAPP aggregates could be achieved by irradiating the system under very mild conditions for less than 30 min, and the IAPP-mediated cytotoxicity was also largely alleviated, providing a new paradigm to accelerate photodynamic degradation of amyloid aggregates for further practical applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Alzheimer's disease research and treatments · Molecular Sensors and Ion Detection · Neuroinflammation and Neurodegeneration Mechanisms
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China
Hubei Key Laboratory of Bioinorganic Chemistry and Materia Medica, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China
Funding
Huazhong University of Science and Technology · Natural Science Foundation of Hubei Province · National Natural Science Foundation of China
References (49)
Show source-provided references
1. 10.1038/nrneurol.2017.510.1038/nrneurol.2017.5 ↗
2. 10.1146/annurev.biochem.75.101304.12390110.1146/annurev.biochem.75.101304.123901 ↗
3. 10.1126/science.107299410.1126/science.1072994 ↗
4. 10.1038/nature0853810.1038/nature08538 ↗
5. 10.2217/nmt-2017-002810.2217/nmt-2017-0028 ↗
6. 10.1016/j.tem.2015.11.00310.1016/j.tem.2015.11.003 ↗
7. 10.1016/j.coph.2018.08.01610.1016/j.coph.2018.08.016 ↗
8. 10.1021/acs.bioconjchem.8b0079710.1021/acs.bioconjchem.8b00797 ↗
9. 10.1021/acsami.8b1107810.1021/acsami.8b11078 ↗
10. 10.1007/s12274-017-1930-710.1007/s12274-017-1930-7 ↗
11. 10.1002/chem.20140007910.1002/chem.201400079 ↗
12. 10.1038/s42004-018-0025-z10.1038/s42004-018-0025-z ↗
13. 10.1038/s41598-018-22820-w10.1038/s41598-018-22820-w ↗
14. 10.1371/journal.pone.011304110.1371/journal.pone.0113041 ↗
15. 10.1021/acsbiomaterials.8b0138410.1021/acsbiomaterials.8b01384 ↗
16. 10.1021/ja504031d10.1021/ja504031d ↗
17. 10.1038/nm.246010.1038/nm.2460 ↗
18. 10.1038/ncomms999710.1038/ncomms9997 ↗
19. 10.1007/s00125-008-1255-x10.1007/s00125-008-1255-x ↗
20. 10.1001/jama.2009.186610.1001/jama.2009.1866 ↗
21. 10.1023/A:102183230252410.1023/A:1021832302524 ↗
22. 10.1371/journal.pbio.100134610.1371/journal.pbio.1001346 ↗
23. 10.1016/j.molcel.2015.07.01210.1016/j.molcel.2015.07.012 ↗
24. 10.1021/acs.jpcb.5b0000610.1021/acs.jpcb.5b00006 ↗
25. 10.1038/nsmb.143710.1038/nsmb.1437 ↗
26. 10.1021/bi060074910.1021/bi0600749 ↗
27. 10.1038/s41557-018-0164-y10.1038/s41557-018-0164-y ↗
28. 10.31635/ccschem.020.20200056110.31635/ccschem.020.202000561 ↗
29. 10.1073/pnas.091072310710.1073/pnas.0910723107 ↗
30. 10.1002/prot.2421610.1002/prot.24216 ↗
31. 10.1110/ps.036509.10810.1110/ps.036509.108 ↗
32. 10.1021/bi900506b10.1021/bi900506b ↗
33. 10.1016/j.actbio.2017.11.04810.1016/j.actbio.2017.11.048 ↗
34. 10.1039/C4CC03791J10.1039/C4CC03791J ↗
35. 10.1002/adfm.20180281310.1002/adfm.201802813 ↗
36. 10.1021/jacs.9b1063210.1021/jacs.9b10632 ↗
37. 10.1021/acs.nanolett.9b0093410.1021/acs.nanolett.9b00934 ↗
38. 10.1021/jacs.0c0839510.1021/jacs.0c08395 ↗
39. 10.1016/j.talanta.2018.08.03710.1016/j.talanta.2018.08.037 ↗
40. 10.1021/acsami.8b1034310.1021/acsami.8b10343 ↗
41. 10.1016/j.biomaterials.2014.10.05810.1016/j.biomaterials.2014.10.058 ↗
42. 10.1016/j.bbrep.2015.07.01710.1016/j.bbrep.2015.07.017 ↗
43. 10.1002/adhm.20150096410.1002/adhm.201500964 ↗
44. 10.1039/c3cc46772d10.1039/c3cc46772d ↗
45. 10.1002/asia.20110042110.1002/asia.201100421 ↗
46. 10.1002/adfm.20190267310.1002/adfm.201902673 ↗
47. 10.1038/s41565-018-0203-210.1038/s41565-018-0203-2 ↗
48. 10.7554/eLife.1297710.7554/eLife.12977 ↗
49. 10.1021/bi700483410.1021/bi7004834 ↗