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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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 |