Rapid Fragmentation during Seeded Lysozyme Aggregation Revealed at the Single Molecule Level.
Journal
Analytical chemistry
ISSN: 1520-6882
Titre abrégé: Anal Chem
Pays: United States
ID NLM: 0370536
Informations de publication
Date de publication:
21 05 2019
21 05 2019
Historique:
pubmed:
20
4
2019
medline:
26
9
2020
entrez:
20
4
2019
Statut:
ppublish
Résumé
Protein aggregation is associated with neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. The poorly understood pathogenic mechanism of amyloid diseases makes early stage diagnostics or therapeutic intervention a challenge. Seeded polymerization that reduces the duration of the lag phase and accelerates fibril growth is a widespread model to study amyloid formation. Seeding effects are hypothesized to be important in the "infectivity" of amyloids and are linked to the development of systemic amyloidosis in vivo. The exact mechanism of seeding is unclear yet critical to illuminating the propagation of amyloids. Here we report on the lateral and axial fragmentation of seed fibrils in the presence of lysozyme monomers at short time scales, followed by the generation of oligomers and growth of fibrils.
Identifiants
pubmed: 30999745
doi: 10.1021/acs.analchem.9b01221
doi:
Substances chimiques
Amyloidogenic Proteins
0
Protein Aggregates
0
hen egg lysozyme
EC 3.2.1.-
Muramidase
EC 3.2.1.17
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM