Literature DB >> 30999745

Rapid Fragmentation during Seeded Lysozyme Aggregation Revealed at the Single Molecule Level.

Markéta Kubánková1, Xiaoyan Lin1, Tim Albrecht1,2, Joshua B Edel1, Marina K Kuimova1.   

Abstract

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.

Entities:  

Year:  2019        PMID: 30999745     DOI: 10.1021/acs.analchem.9b01221

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  1 in total

1.  Real-Time Fast Amyloid Seeding and Translocation of α-Synuclein with a Nanopipette.

Authors:  Nathan Meyer; Jean-Marc Janot; Joan Torrent; Sébastien Balme
Journal:  ACS Cent Sci       Date:  2022-02-23       Impact factor: 18.728

  1 in total

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