| Texto completo | |
| Autor(es): |
de Oliveira, Osmair Vital
;
Goncalves, Arlan da Silva
;
Castilho de Almeida, Natalia Ellen
Número total de Autores: 3
|
| Tipo de documento: | Artigo Científico |
| Fonte: | JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS; v. 40, n. 20, p. 11-pg., 2022-01-01. |
| Resumo | |
In this study, comparable molecular dynamic (MD) simulations of 1.2 microseconds were performed to clarify the prevention of the b-amyloid peptide (A beta(1-42)) aggregation by cucurbit[7]uril (CB[7]). The accumulation of this peptide in the brain is one of the most harmful in Alzheimer's disease. The inhibition mechanism of A beta(1-42) aggregation by different molecules is attributed to preventing of Ab1- 42 conformational transition from a-helix to the b-sheet structure. However, our structural analysis shows that the pure water and aqueous solution of the CB[7] denature the native A beta(1-42) a-helix structure forming different compactness and unfolded conformations, not in b-sheet form. On the other hand, in the three CB[7]@Ab1- 42 complexes, it was observed the encapsulation of N-terminal (Asp1), Lys16, and Val36 by CB[7] along the MD trajectory, and not with aromatic residues as suggested by the literature. Only in one CB[7]@A beta(1-42) complex was observed stable Asp23-Lys28 salt bridge with an average distance of 0.36 nm. All CB[7]@A beta(1-42) complexes are very stable with binding free energy lowest than similar to-50 kcal/mol between the CB[7] and A beta(1-42) monomer from MM/PBSA calculation. Therefore, herein we show that the mechanism of the prevention of elongation protofibril by CB[7] is due to the disruption of the Asp23-Lys28 salt bridge and steric effects of CB[7]@A beta(1-42) complex with the fibril lattice, and not due to the transition from a-helix to b-sheet following the dock-lock mechanism. (AU) | |
| Processo FAPESP: | 18/19844-8 - Estudo Molecular do Encapsulamento de Compostos Bioativos na Cucurbit[7]urila |
| Beneficiário: | Osmair Vital de Oliveira |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |