The impact of membrane composition on conformation and trafficking of lipidated prion protein (PrP) variants
Prion protein (PrP) aggregation arises from the misfolding of the native cellular PrP (PrPC) and is a key pathophysiologic event in fatal neurodegenerative prion diseases. To elucidate the mechanism of conversion of PrPC into toxic PrPSc, homogeneous PrP constructs carrying a glycosylphosphatidylino...
Main Author: | Hackl, Stefanie |
---|---|
Other Authors: | Cho Nam-Joon |
Format: | Thesis-Doctor of Philosophy |
Language: | English |
Published: |
Nanyang Technological University
2020
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/136871 |
Similar Items
-
The impact of membrane composition on conformation and trafficking of lipidated prion protein (PrP) variants
by: Hackl, Stefanie
Published: (2020) -
Context Dependent Neuroprotective Properties of Prion Protein (Prp)
by: Steele, Andrew D., et al.
Published: (2011) -
Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases
by: Jackson, Walker S., et al.
Published: (2014) -
Graphene quantum dots as universal fluorophores and their use in revealing regulated trafficking of insulin receptors in adipocytes
by: Zheng, Xin Ting, et al.
Published: (2013) -
A proteomics and metabolomics analysis of the mechanism of lipid accumulation in yeast
by: Shi, Jiahua
Published: (2015)