The molecular processes underpinning prion-like spreading and seed amplification in protein aggregation. (April 2020)

• Record Type: Journal Article
• Authors: Meisl, Georg; Knowles, Tuomas PJ; Klenerman, David
• Is Part Of: Current opinion in neurobiology. Volume 61(2020)
• Page Start: 58
• Page End: 64
• Publication Date: 2020-04
• Subjects: Neurobiology -- Periodicals; 573.8
• DOI: 10.1016/j.conb.2020.01.010
• Languages: English
• ISSNs: 0959-4388

Abstract

Highlights: Kinetics yield mechanism and rates of aggregation of tau, PrP, Aβ and α-syn in vitro . Animal models provide evidence for differences and similarities in mechanisms in vivo . Mathematical models of spreading/replication can connect in vitro to human disease. Additional detail and information from experiment is needed for a quantitative model. Abstract : The formation of aggregates from a range of normally soluble peptides and proteins is the hallmark of several neurodegenerative disorders, including Parkinson's and Alzheimer's diseases. Certain such aggregates possess the ability to replicate and spread pathology, within tissues and in some case also between organisms. An understanding of which processes govern the overall rate of aggregate formation is thus of key interest. Here, we discuss the fundamental molecular processes of protein aggregation, review how their rates can be determined by kinetic measurements in the test-tube, and explore the mechanistic similarities and differences to animal models and human disease. We conclude that a quantitative mathematical model for aggregate replication and spreading in vivo requires additional information but would provide a theoretical framework to understand results from different experiments and how they connect to human disease.