Thioflavin-T is used to image amyloid aggregates because of the excellent turn-on fluorescence properties, but binding affinities are low. By mounting multiple dye units on the surface of a vesicle, the binding affinity for α-synuclein fibrils is increased by three orders of magnitude, and the optical response is increased. Cooperative interactions of the dye headgroup and lipid with the protein provide a general strategy for the construction of multivalent amyloid probes based on vesicles.Engineering and Physical Sciences Research Council (EP/R005397/1 and EP/P008224/1)
Amyloid fibrils and tangles are signatures of Alzheimer disease, but nanometer-sized aggregation int...
Amyloid fibrils and tangles are signatures of Alzheimer disease, but nanometer-sized aggregation int...
The characterization of the aggregation kinetics of protein amyloids and the structural properties o...
Alzheimer’s disease (AD) is characterised by a series of biomolecular aggregation events, which incl...
Amyloid fibrils are long fibrillar homopolymers of self-assembled proteins. They can be formed by es...
Amyloid fibrils are long fibrillar homopolymers of self-assembled proteins. They can be formed by es...
Neurodegenerative diseases such as Alzheimer's and Parkinson's are associated with protein misfoldin...
Formation of amyloid fibrils underlies a wide range of human disorders, including Alzheimer's and pr...
Formation of amyloid fibrils underlies a wide range of human disorders, including Alzheimer's and pr...
Formation of amyloid fibrils underlies a wide range of human disorders, including Alzheimer's and pr...
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
Integration of two fluorescence imaging methods enables tracking of the formation of fibrillar Aβ pe...
Highly ordered protein aggregates, termed amyloid fibrils, are associated with a broad range of dise...
There is currently no definitive test for early detection of neurodegeneration which is linked with ...
Amyloid protein aggregation results in major disturbances of cellular processes in humans. The most ...
Amyloid fibrils and tangles are signatures of Alzheimer disease, but nanometer-sized aggregation int...
Amyloid fibrils and tangles are signatures of Alzheimer disease, but nanometer-sized aggregation int...
The characterization of the aggregation kinetics of protein amyloids and the structural properties o...
Alzheimer’s disease (AD) is characterised by a series of biomolecular aggregation events, which incl...
Amyloid fibrils are long fibrillar homopolymers of self-assembled proteins. They can be formed by es...
Amyloid fibrils are long fibrillar homopolymers of self-assembled proteins. They can be formed by es...
Neurodegenerative diseases such as Alzheimer's and Parkinson's are associated with protein misfoldin...
Formation of amyloid fibrils underlies a wide range of human disorders, including Alzheimer's and pr...
Formation of amyloid fibrils underlies a wide range of human disorders, including Alzheimer's and pr...
Formation of amyloid fibrils underlies a wide range of human disorders, including Alzheimer's and pr...
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
Integration of two fluorescence imaging methods enables tracking of the formation of fibrillar Aβ pe...
Highly ordered protein aggregates, termed amyloid fibrils, are associated with a broad range of dise...
There is currently no definitive test for early detection of neurodegeneration which is linked with ...
Amyloid protein aggregation results in major disturbances of cellular processes in humans. The most ...
Amyloid fibrils and tangles are signatures of Alzheimer disease, but nanometer-sized aggregation int...
Amyloid fibrils and tangles are signatures of Alzheimer disease, but nanometer-sized aggregation int...
The characterization of the aggregation kinetics of protein amyloids and the structural properties o...