| Literature DB >> 30817076 |
Han Sun1,2,3, Jing Liu4, Shengliang Li1, Lingyun Zhou1,3, Jianwu Wang1,2,3, Libing Liu1, Fengting Lv1, Qi Gu4, Baoyang Hu4, Yuguo Ma2, Shu Wang1,3.
Abstract
Protein misfolding and aberrant aggregations are associated with multiple prevalent and intractable diseases. Inhibition of amyloid assembly is a promising strategy for the treatment of amyloidosis. Reported here is the design and synthesis of a reactive conjugated polymer, a poly(p-phenylene vinylene) derivative, functionalized with p-nitrophenyl esters (PPV-NP) and it inhibits the assembly of amyloid proteins, degrades preformed fibrils, and reduces the cytotoxicity of amyloid aggregations in living cells. PPV-NP is attached to the proteins through hydrophobic interactions and irreversible covalent linkage. PPV-NP also exhibited the capacity to eliminate Aβ plaques in brain slices in ex vivo assays. This work represents an innovative attempt to inhibit protein pathogenic aggregates, and may offer insights into the development of therapeutic strategies for amyloidosis.Entities:
Keywords: aggregation; fibrils; hydrophobic effects; polymers; proteins
Year: 2019 PMID: 30817076 DOI: 10.1002/anie.201901459
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336