AbstractWe introduce a stochastic model describing aggregation of misfolded proteins and degradation by the protein quality control system in a single cell. Aggregate growth is contrasted by the cell quality control system, that attacks them at different stages of the growth process, with an efficiency that decreases with their size. Model parameters are estimated from experimental data. Two qualitatively different behaviors emerge: a homeostatic state, where the quality control system is stable and aggregates of large sizes are not formed, and an oscillatory state, where the quality control system periodically breaks down, allowing for formation of large aggregates. We discuss how these periodic breakdowns may constitute a mechanism for th...
Protein aggregation trends in neurodegenerative diseases are largely unmapped due to the complex nat...
The inability of a protein to adopt its native and soluble conformation (protein misfolding) is the ...
Amyloid fibrils and soluble oligomers are two types of protein aggregates associated with neurodegen...
AbstractWe introduce a stochastic model describing aggregation of misfolded proteins and degradation...
Protein aggregates are hallmarks of neurodegenerative diseases. The protein quality control (PQC) sy...
Self-assembly of proteins into amyloid aggregates is an important biological phenomenon associated w...
Fibrillar protein aggregation is a hallmark of a variety of human diseases. Examples include the dep...
The deposition of pathological protein aggregates in the brain plays a central role in cognitive dec...
AbstractThe nucleation-growth model has been used extensively for characterizing in vitro amyloid fi...
Autocatalytic fibril nucleation has recently been proposed to be a determining factor for the spread...
Overexpression of the de-ubiquitinating enzyme UCH-L1 leads to inclusion formation in response to pr...
The generation of toxic non-native protein conformers has emerged as a unifying thread among disorde...
Protein aggregation is linked with neurodegeneration and numerous other diseases by mechanisms that ...
SummaryProtein aggregation is linked with neurodegeneration and numerous other diseases by mechanism...
An increasing number of proteins are being shown to assemble into amyloid structures, self-seeding f...
Protein aggregation trends in neurodegenerative diseases are largely unmapped due to the complex nat...
The inability of a protein to adopt its native and soluble conformation (protein misfolding) is the ...
Amyloid fibrils and soluble oligomers are two types of protein aggregates associated with neurodegen...
AbstractWe introduce a stochastic model describing aggregation of misfolded proteins and degradation...
Protein aggregates are hallmarks of neurodegenerative diseases. The protein quality control (PQC) sy...
Self-assembly of proteins into amyloid aggregates is an important biological phenomenon associated w...
Fibrillar protein aggregation is a hallmark of a variety of human diseases. Examples include the dep...
The deposition of pathological protein aggregates in the brain plays a central role in cognitive dec...
AbstractThe nucleation-growth model has been used extensively for characterizing in vitro amyloid fi...
Autocatalytic fibril nucleation has recently been proposed to be a determining factor for the spread...
Overexpression of the de-ubiquitinating enzyme UCH-L1 leads to inclusion formation in response to pr...
The generation of toxic non-native protein conformers has emerged as a unifying thread among disorde...
Protein aggregation is linked with neurodegeneration and numerous other diseases by mechanisms that ...
SummaryProtein aggregation is linked with neurodegeneration and numerous other diseases by mechanism...
An increasing number of proteins are being shown to assemble into amyloid structures, self-seeding f...
Protein aggregation trends in neurodegenerative diseases are largely unmapped due to the complex nat...
The inability of a protein to adopt its native and soluble conformation (protein misfolding) is the ...
Amyloid fibrils and soluble oligomers are two types of protein aggregates associated with neurodegen...