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Molecular Dynamics of Lysozyme Amyloid Polymorphs Studied by Incoherent Neutron Scattering

Lysozyme amyloidosis is a hereditary disease, which is characterized by the deposition of lysozyme amyloid fibrils in various internal organs. It is known that lysozyme fibrils show polymorphism and that polymorphs formed at near-neutral pH have the ability to promote more monomer binding than those...

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Detalles Bibliográficos
Autores principales: Matsuo, Tatsuhito, De Francesco, Alessio, Peters, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801425/
https://www.ncbi.nlm.nih.gov/pubmed/35111814
http://dx.doi.org/10.3389/fmolb.2021.812096