Apomyoglobin reveals a random-nucleation mechanism in amyloid protofibril formation

• Published in: Acta histochemica Vol. 108; no. 3; pp. 215 - 219
• Main Authors: Fändrich, Marcus, Zandomeneghi, Giorgia, Krebs, Mark R.H., Kittler, Marlis, Buder, Katrin, Roßner, Angela, Heinemann, Stefan H., Dobson, Christopher M., Diekmann, Stephan
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.01.2006
• Subjects: Aggregation; Amyloid; Amyloid - chemistry; Amyloid - ultrastructure; Animals; Apomyoglobin; Apoproteins - chemistry; Horses; Microscopy, Atomic Force; Microscopy, Electron, Transmission; Models, Molecular; Myoglobin - chemistry; Protein Conformation; Protein Folding; Protofibrils; Aggregation; Amyloid; Protein folding; Apomyoglobin; Protofibrils
• ISSN: 0065-1281; 1618-0372
• DOI: 10.1016/j.acthis.2006.03.012

Protofibrils (PFs) represent the earliest fibrillar species that occur in the course of amyloid fibril formation. Using apomyoglobin, we report here that PFs arise from a multi-step reaction and that they are preceded by an ensemble of non-fibrillar particles (NFPs). These intermediate aggregates encompass nascent elements of amyloid structure and can act as seeds in PF formation. Taken together with the observation that PFs often protrude from NFPs, our data suggest that PFs form by a random nucleation mechanism in which the polypeptide chains sample many different aggregated conformations. Once the appropriate structural characteristics are acquired, PFs are formed by addition of further polypeptide chains.