Abstract
Amyloid fibrils are insoluble protein aggregates comprised of highly ordered β-sheet structures and they are involved in the pathology of amyloidoses, such as Alzheimer's disease. A supramolecular strategy is presented for inhibiting amyloid fibrillation by using cucurbit[7]uril (CB[7]). CB[7] prevents the fibrillation of insulin and β-amyloid by capturing phenylalanine (Phe) residues, which are crucial to the hydrophobic interactions formed during amyloid fibrillation. These results suggest that the Phe-specific binding of CB[7] can modulate the intermolecular interaction of amyloid proteins and prevent the transition from monomeric to multimeric states. CB[7] thus has potential for the development of a therapeutic strategy for amyloidosis.
Original language | English |
---|---|
Pages (from-to) | 7461-7465 |
Number of pages | 5 |
Journal | Angewandte Chemie - International Edition |
Volume | 53 |
Issue number | 29 |
DOIs | |
Publication status | Published - 2014 Jul 14 |
Externally published | Yes |
Keywords
- aggregation
- cucurbit[7]uril
- insulin
- supramolecular chemistry
- β-amyloid
ASJC Scopus subject areas
- Catalysis
- Chemistry(all)