journal article·2019-07-03

Reactive Conjugated Polymers for the Modulation of Islet Amyloid Polypeptide Assembly

Han Sun, Fengting Lv, Libing Liu, Shu Wang

ACS Applied Materials & Interfaces· Volume 11· Issue 26
Publisher page

Abstract

Misfolding and abnormal assembly of proteins cause many intractable diseases. The modulation of the assembly process of these proteins could contribute to understanding and controlling amyloid protein aggregation. Previous works focused mainly on the inhibition of the assembly process. To broaden the interaction modality of modulators with proteins for developing new modulators, in this work, we designed and synthesized two reactive poly ( p-phenylene vinylene) polymers, respectively, functionalized with N-hydroxysuccinimide ester (PPV-NHS) and pentafluorophenol ester (PPV-PFP), which exhibited the prevention or co-assembly effect on the aggregation process of islet amyloid polypeptide (IAPP). Cell assays demonstrated that both of the two polymers could effectively eliminate the cytotoxicity of IAPP. Moreover, PPV-NHS also could irreversibly disrupt preformed IAPP fibrils. We envision that PPV-NHS and PPV-PFP might offer a new design method for the modulation of protein assembly.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Chemical Synthesis and Analysis · Advanced Polymer Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100910, P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing 100049, P. R. China

Funding

National Natural Science Foundation of China · Chinese Academy of Sciences

References (24)

Show source-provided references
1. 10.1038/s41580-018-0060-810.1038/s41580-018-0060-8 ↗
2. 10.1038/nrd459310.1038/nrd4593 ↗
3. 10.1038/ncomms1141210.1038/ncomms11412 ↗
4. 10.1038/nchem.255010.1038/nchem.2550 ↗
5. 10.1021/jacs.5b1260010.1021/jacs.5b12600 ↗
6. 10.1002/anie.20100782410.1002/anie.201007824 ↗
7. 10.1038/s41565-018-0179-y10.1038/s41565-018-0179-y ↗
8. 10.1021/acschemneuro.6b0034910.1021/acschemneuro.6b00349 ↗
9. 10.1126/sciadv.170048810.1126/sciadv.1700488 ↗
10. 10.1073/pnas.160721511410.1073/pnas.1607215114 ↗
11. 10.1021/acs.biomac.8b0067110.1021/acs.biomac.8b00671 ↗
12. 10.1002/anie.20140073510.1002/anie.201400735 ↗
13. 10.1021/acsami.6b0366810.1021/acsami.6b03668 ↗
14. 10.1021/cb900112v10.1021/cb900112v ↗
15. 10.1002/cbic.20050055010.1002/cbic.200500550 ↗
16. 10.1002/adfm.20160162110.1002/adfm.201601621 ↗
17. 10.1002/aelm.20170016110.1002/aelm.201700161 ↗
18. 10.1039/B712829K10.1039/B712829K ↗
19. 10.1152/physrev.00042.200910.1152/physrev.00042.2009 ↗
20. 10.1155/2016/279826910.1155/2016/2798269 ↗
21. 10.1002/anie.20190145910.1002/anie.201901459 ↗
22. 10.1002/anie.20180115510.1002/anie.201801155 ↗
23. 10.1021/ja804180610.1021/ja8041806 ↗
24. 10.1021/ja206279b10.1021/ja206279b ↗