AbstractSeveral widespread and severe degenerative diseases are characterized by the deposition of amyloid protein aggregates in affected tissues. While there is great interest in the complete description of the aggregation pathway of the proteins involved, a molecular level understanding is hindered by the complexity of the self-assembly process. In particular, the early stages of aggregation, where dynamic, heterogeneous and often toxic intermediates are populated, are resistant to high-resolution structural characterization. Fluorescence spectroscopy is a powerful and versatile tool for such analysis. In this review, we survey its application to provide residue-specific information about amyloid intermediate states for three selected pro...
Misfolding and aggregation of proteins are characteristics of a range of increasingly prevalent neur...
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
AbstractThe mechanisms linking deposits of insoluble amyloid fibrils to the debilitating neuronal ce...
AbstractSeveral widespread and severe degenerative diseases are characterized by the deposition of a...
Protein amyloid aggregation has been associated with more than 50 human disorders, including the mos...
The defining feature of the extensive family of amyloid diseases is the formation of networks of ent...
The aggregation of a -synuclein is associated with progression of Parkinson’s disease. We have ident...
A number of proteins are capable of converting from their soluble, monomeric form into highly-ordere...
Highly ordered protein aggregates, termed amyloid fibrils, are associated with a broad range of dise...
Oligomers which form during amyloid fibril assembly are considered to be key contributors towards am...
Amyloidosis is a group of diseases in which amyloid fibrils accumulate and deposit into plaques and ...
Misfolding and aggregation of proteins are characteristics of a range of increasingly prevalent neur...
The amyloid formation of the folded segment of a variant of Exenatide (a marketed drug for Type-2 Di...
The aggregation of proteins into insoluble filamentous amyloid fibrils is a pathological hallmark of...
Many neurodegenerative disorders, including Alzheimer''s, Parkinson''s and the prion diseases, are c...
Misfolding and aggregation of proteins are characteristics of a range of increasingly prevalent neur...
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
AbstractThe mechanisms linking deposits of insoluble amyloid fibrils to the debilitating neuronal ce...
AbstractSeveral widespread and severe degenerative diseases are characterized by the deposition of a...
Protein amyloid aggregation has been associated with more than 50 human disorders, including the mos...
The defining feature of the extensive family of amyloid diseases is the formation of networks of ent...
The aggregation of a -synuclein is associated with progression of Parkinson’s disease. We have ident...
A number of proteins are capable of converting from their soluble, monomeric form into highly-ordere...
Highly ordered protein aggregates, termed amyloid fibrils, are associated with a broad range of dise...
Oligomers which form during amyloid fibril assembly are considered to be key contributors towards am...
Amyloidosis is a group of diseases in which amyloid fibrils accumulate and deposit into plaques and ...
Misfolding and aggregation of proteins are characteristics of a range of increasingly prevalent neur...
The amyloid formation of the folded segment of a variant of Exenatide (a marketed drug for Type-2 Di...
The aggregation of proteins into insoluble filamentous amyloid fibrils is a pathological hallmark of...
Many neurodegenerative disorders, including Alzheimer''s, Parkinson''s and the prion diseases, are c...
Misfolding and aggregation of proteins are characteristics of a range of increasingly prevalent neur...
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
AbstractThe mechanisms linking deposits of insoluble amyloid fibrils to the debilitating neuronal ce...