RT Journal Article
SR Electronic
T1 A protease protection assay for the detection of internalized alpha-synuclein pre-formed fibrils
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2020.10.12.335885
DO 10.1101/2020.10.12.335885
A1 Timothy S. Jarvela
A1 Kriti Chaplot
A1 Iris Lindberg
YR 2020
UL http://biorxiv.org/content/early/2020/10/12/2020.10.12.335885.abstract
AB Alpha-synuclein pre-formed fibrils (PFFs) represent a promising model system for the study of cellular processes underlying cell-to-cell transmission of α-synuclein proteopathic aggregates. However, the ability to differentiate the fate of internalized PFFs from those which remain in the extracellular environment remains limited due to the propensity for PFFs to adhere to the cell surface. Removal of PFFs requires repeated washing and/or specific quenching of extracellular fluorescent PFF signals. In this paper we present a new method for analyzing the fate of internalized α-synuclein. We inserted a tobacco etch virus (TEV) protease cleavage site between α-synuclein and green fluorescent protein. As the TEV protease is highly specific, non-toxic, and active under physiological conditions, we are able to use protection from TEV cleavage to distinguish internalized PFFs from those which remain attached to the cell surface. Using this experimental paradigm, downstream intracellular events can be analyzed via live or fixed cell microscopy as well as by Western blotting. We suggest that this method will be useful for understanding the fate of PFFs after endocytosis under various experimental manipulations.