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Super-resolution imaging of alpha-synuclein polymorphisms and their potential role in neurodegeneration

Accepted version
Peer-reviewed

Type

Article

Change log

Authors

Kaminski, CF 
Kaminski Schierle, GS 

Abstract

The conversion of soluble, functional proteins into amyloid fibrils has been linked to the development of neurodegenerative disorders, including Parkinson's and Alzheimer's disease. In the brains of patients with these disorders, the increasing presence of amyloid-containing plaques corresponds to neuronal cell death and the worsening of symptoms. However, protein amyloids are not merely confined to dying cells. Rather, some show a propensity to be transmitted to, and enter adjacent cells and induce the polymerization of the native monomer population. Whether this process is directly associated with toxicity or not is still highly debated. In this mini review, we will discuss structural polymorphisms of α-synuclein, as determined by super-resolution imaging techniques, and how these may be related to neuronal toxicity.

Description

Keywords

Brain, Calcium-Binding Proteins, Image Enhancement, Membrane Proteins, Microscopy, Molecular Imaging, Muscle Proteins, Neurodegenerative Diseases, Polymorphism, Single Nucleotide

Journal Title

Integrative Biology

Conference Name

Journal ISSN

1757-9694
1757-9708

Volume Title

9

Publisher

Royal Society of Chemistry
Sponsorship
Engineering and Physical Sciences Research Council (EP/H018301/1)
Medical Research Council (MR/K02292X/1)
Medical Research Council (MR/K015850/1)
Wellcome Trust (089703/Z/09/Z)
Wellcome Trust (203249/Z/16/Z)
This work was funded by grants from the UK Medical Research Council (MR/K015850/1 and MR/K02292X/1), Alzheimer’s Research UK (ARUK-EG2012A-1), the UK Engineering and Physical Sciences Research Council (EP/H018301/1), and the Wellcome Trust (089703/ Z/09/Z).