Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Methods Mol Biol ; 2340: 139-173, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35167074

RESUMO

The amyloid ß-protein is an intrinsically disordered protein that has the potential to assemble into myriad structures, including oligomers and fibrils. These structures are neurotoxic and are thought to initiate a cascade of events leading to Alzheimer's disease. Understanding this pathogenetic process and elucidating targets for drug therapy depends on elucidation of the structural dynamics of Aß assembly. In this chapter, we describe work packages required to determine the three-dimensional structures of Aß and of smaller bioactive fragments thereof, which may be important in AD pathogenesis. These packages include density functional theory, Car-Parrinello molecular dynamics simulations, temperature-dependent replica exchange molecular dynamics simulations, disorder predictors based on bioinformatics, and neural network deep learning.


Assuntos
Doença de Alzheimer , Doenças Neurodegenerativas , Peptídeos beta-Amiloides , Inteligência Artificial , Biologia Computacional , Humanos , Simulação de Dinâmica Molecular , Fragmentos de Peptídeos
2.
Phys Chem Chem Phys ; 20(48): 30525-30536, 2018 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-30512023

RESUMO

The self assembly processes of aromatic amino acids, phenylalanine, tyrosine, and tryptophan have been simulated and were observed to form fibril-like aggregates linked to certain rare diseases and instances of biological membrane disruption. Pure systems and their mixtures were studied systematically at constant temperatures and free energy landscapes were produced describing the height and the number of assembled monomers associated with lower energy structures. Consistent with some previous work, aromatic amino acid monomers display a tendency to arrange with a four-fold symmetry. The occurrence of this and other ordered structures increases at higher temperatures. At lower temperatures our binary mixture simulations indicate that increasing tryptophan content drives the assembly process away from the formation of distinct nanostructures and toward disordered aggregates which is in line with experimental observations of pure tryptophan solutions. This work provides molecular level insight to a variety of different physical phenomena relevant to fields including human disease.


Assuntos
Aminoácidos Aromáticos/química , Substâncias Macromoleculares/química , Ligação de Hidrogênio , Interações Hidrofóbicas e Hidrofílicas , Simulação de Dinâmica Molecular , Fenilalanina/química , Estereoisomerismo , Temperatura , Triptofano/química , Tirosina/química , Água/química
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...