Protein aggregation is a hallmark of major neurodegenerative disorders. Increasing data suggest that smaller aggregates cause higher toxic response than filamentous aggregates (fibrils). However, the size of small aggregates has challenged their detection within biologically relevant environments. Here, we report approaches to quantitatively super-resolve aggregates in live cells and ex vivo brain tissues. We show that Amytracker 630 (AT630), a commercial aggregate-activated fluorophore, has outstanding photophysical properties that enable super-resolution imaging of α-synuclein, tau, and amyloid-β aggregates, achieving ∼4 nm precision. Applying AT630 to AppNL-G-F mouse brain tissues or aggregates extracted from a Parkinson's disease donor,...
There is now crucial medical importance placed on understanding the role of early stage, subvisible ...
Protein aggregation is a complex process resulting in the formation of heterogeneous mixtures of agg...
Self-assembly of α−synuclein resulting in protein aggregates of diverse morphology has been implicat...
Protein aggregates play a key role in the initiation and spreading of neurodegenerative disease but ...
Soluble α-synuclein aggregates varying in size, structure, and morphology have been closely linked t...
Protein aggregation is a complex process resulting in the formation of heterogeneous mixtures of agg...
The misfolding and aggregation of proteins into amyloid fibrils characterizes many neurodegenerative...
The aberrant misfolding and subsequent conversion of monomeric protein into amyloid aggregates chara...
Funder: Royal Society; doi: https://doi.org/10.13039/501100000288Funder: UK Dementia Research Instit...
Aggregation of α-synuclein plays a key role in the development of Parkinson's disease. Soluble aggre...
α-Synuclein (αS) is an intrinsically disordered and highly dynamic protein involved in dopamine rele...
Aggregation of α-synuclein plays a key role in the development of Parkinson’s disease. Soluble aggre...
Protein aggregation is a key molecular feature underlying a wide array of neurodegenerative disorder...
The morphological features of α-synuclein (AS) amyloid aggregation in vitro and in cells were elucid...
Proteins fold into a single structural ensemble but can also misfold into many diverse structures in...
There is now crucial medical importance placed on understanding the role of early stage, subvisible ...
Protein aggregation is a complex process resulting in the formation of heterogeneous mixtures of agg...
Self-assembly of α−synuclein resulting in protein aggregates of diverse morphology has been implicat...
Protein aggregates play a key role in the initiation and spreading of neurodegenerative disease but ...
Soluble α-synuclein aggregates varying in size, structure, and morphology have been closely linked t...
Protein aggregation is a complex process resulting in the formation of heterogeneous mixtures of agg...
The misfolding and aggregation of proteins into amyloid fibrils characterizes many neurodegenerative...
The aberrant misfolding and subsequent conversion of monomeric protein into amyloid aggregates chara...
Funder: Royal Society; doi: https://doi.org/10.13039/501100000288Funder: UK Dementia Research Instit...
Aggregation of α-synuclein plays a key role in the development of Parkinson's disease. Soluble aggre...
α-Synuclein (αS) is an intrinsically disordered and highly dynamic protein involved in dopamine rele...
Aggregation of α-synuclein plays a key role in the development of Parkinson’s disease. Soluble aggre...
Protein aggregation is a key molecular feature underlying a wide array of neurodegenerative disorder...
The morphological features of α-synuclein (AS) amyloid aggregation in vitro and in cells were elucid...
Proteins fold into a single structural ensemble but can also misfold into many diverse structures in...
There is now crucial medical importance placed on understanding the role of early stage, subvisible ...
Protein aggregation is a complex process resulting in the formation of heterogeneous mixtures of agg...
Self-assembly of α−synuclein resulting in protein aggregates of diverse morphology has been implicat...