Aggregation of amyloidogenic proteins causing neurodegenerative diseases is an uncontrollable and contagious process that is often associated with lipid membranes in a highly complex physiological environment. Although several approaches using natural cells and membrane models have been reported, systematic investigations focusing on the association with the membranes are highly challenging, mostly because of the lack of proper molecular tools. Here, we report a new supramolecular approach using a synthetic cell system capable of controlling the initiation of protein aggregation and mimicking various conditions of lipid membranes, thereby enabling systematic investigations of membrane-dependent effects on protein aggregation by visualizatio...
In this paper, we discuss amyloidogenic proteins, their misfolding, resulting structures, and intera...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
The conversion of otherwise soluble proteins into insoluble amyloid aggregates is associated with a ...
© 2021 American Chemical Society. All rights reserved.Aggregation of amyloidogenic proteins causing ...
Aggregation of amyloidogenic proteins causingneurodegenerative diseases is an uncontrollable and con...
The misfolding and aggregation of proteins is closely associated with more than fifty human disorder...
Lipid membranes play a fundamental role in the pathological development of protein misfolding diseas...
There are a vast number of neurodegenerative diseases, including Alzheimer’s disease (AD), Parkinson...
AbstractPrefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in seve...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
Molecular level self-assembly/aggregation processes are common in biomolecular systems. Specifically...
A number of neurodegenerative diseases are known to involve protein aggregation. Common mechanisms a...
A number of neurodegenerative diseases are known to involve protein aggregation. Common mechanisms a...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
In this paper, we discuss amyloidogenic proteins, their misfolding, resulting structures, and intera...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
The conversion of otherwise soluble proteins into insoluble amyloid aggregates is associated with a ...
© 2021 American Chemical Society. All rights reserved.Aggregation of amyloidogenic proteins causing ...
Aggregation of amyloidogenic proteins causingneurodegenerative diseases is an uncontrollable and con...
The misfolding and aggregation of proteins is closely associated with more than fifty human disorder...
Lipid membranes play a fundamental role in the pathological development of protein misfolding diseas...
There are a vast number of neurodegenerative diseases, including Alzheimer’s disease (AD), Parkinson...
AbstractPrefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in seve...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
Molecular level self-assembly/aggregation processes are common in biomolecular systems. Specifically...
A number of neurodegenerative diseases are known to involve protein aggregation. Common mechanisms a...
A number of neurodegenerative diseases are known to involve protein aggregation. Common mechanisms a...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
In this paper, we discuss amyloidogenic proteins, their misfolding, resulting structures, and intera...
Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neur...
The conversion of otherwise soluble proteins into insoluble amyloid aggregates is associated with a ...