Structural Characterization of N-WASP Domain V Using MD Simulations with NMR and SAXS Data.
Biophys J
; 116(7): 1216-1227, 2019 04 02.
Article
em En
| MEDLINE
| ID: mdl-30878202
ABSTRACT
Because of their large conformational heterogeneity, structural characterization of intrinsically disordered proteins (IDPs) is very challenging using classical experimental methods alone. In this study, we use NMR and small-angle x-ray scattering (SAXS) data with multiple molecular dynamics (MD) simulations to describe the conformational ensemble of the fully disordered verprolin homology domain of the neural Aldrich syndrome protein involved in the regulation of actin polymerization. First, we studied several back-calculation software of SAXS scattering intensity and optimized the adjustable parameters to accurately calculate the SAXS intensity from an atomic structure. We also identified the most appropriate force fields for MD simulations of this IDP. Then, we analyzed four conformational ensembles of neural Aldrich syndrome protein verprolin homology domain, two generated with the program flexible-meccano with or without NMR-derived information as input and two others generated by MD simulations with two different force fields. These four conformational ensembles were compared to available NMR and SAXS data for validation. We found that MD simulations with the AMBER-03w force field and the TIP4P/2005s water model are able to correctly describe the conformational ensemble of this 67-residue IDP at both local and global level.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Proteína da Síndrome de Wiskott-Aldrich
/
Proteínas Intrinsicamente Desordenadas
Limite:
Humans
Idioma:
En
Revista:
Biophys J
Ano de publicação:
2019
Tipo de documento:
Article
País de afiliação:
França