<p>Fluorescence emission intensity accompanying the binding of ThT with amyloid fibrils after 72 h of incubation in the presence of (▪) ThT, (•) ThT + native lysozyme, (▴) ThT + lysozyme aggregates (Panel A); and kinetics of the lysozyme amyloid formation (Panel B), point I shows lysozyme at the native state, point II denotes the end of nucleation period and beginning of the elongation stage, point III shows lysozyme at the middle of the elongation period and points IV, V and VI denotes the saturation stages of lysozyme.</p
Amyloidosis is a group of diseases in which amyloid fibrils accumulate and deposit into plaques and ...
The aggregation of proteins into insoluble filamentous amyloid fibrils is a pathological hallmark of...
<p>Kinetics of lysozyme fibril extension in absence and in presence of different concentration of os...
<p>ThT emission signal recorded at λ = 485 nm vs. time from initiation of the aggregation reaction, ...
Time-resolved fluorescence studies of protein aggregation leading to amyloid formatio
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
Human lysozyme (HuL) is a widely characterised protein whose mutational variants misfold, forming am...
<div><p>Protein aggregation leading to formation of amyloid fibrils is a symptom of several diseases...
<p><b> amyloid formation monitored by ThT fluorescence assay at 23</b><b> (296 K) and pH 2.9 (black ...
<p>A) Fluorescence intensity of the amyloid binding dye ThT as a function of the hαS concentration a...
Highly ordered protein aggregates, termed amyloid fibrils, are associated with a broad range of dise...
<p>A. S100 proteins (1 mg/mL) were incubated at pH 2.5 and 37°C during 160 h without agitation in th...
Amyloid-beta fibrils within the human brain have been reported to be a possible cause for Alzheimer’...
<p>(A) Thioflavin T signal versus time of amyloid β peptides. Peptide samples, at 20 µM and containi...
AbstractThe mechanisms linking deposits of insoluble amyloid fibrils to the debilitating neuronal ce...
Amyloidosis is a group of diseases in which amyloid fibrils accumulate and deposit into plaques and ...
The aggregation of proteins into insoluble filamentous amyloid fibrils is a pathological hallmark of...
<p>Kinetics of lysozyme fibril extension in absence and in presence of different concentration of os...
<p>ThT emission signal recorded at λ = 485 nm vs. time from initiation of the aggregation reaction, ...
Time-resolved fluorescence studies of protein aggregation leading to amyloid formatio
Amyloid deposition has been observed in more than 20 diseases. Each amyloid-related dis...
Human lysozyme (HuL) is a widely characterised protein whose mutational variants misfold, forming am...
<div><p>Protein aggregation leading to formation of amyloid fibrils is a symptom of several diseases...
<p><b> amyloid formation monitored by ThT fluorescence assay at 23</b><b> (296 K) and pH 2.9 (black ...
<p>A) Fluorescence intensity of the amyloid binding dye ThT as a function of the hαS concentration a...
Highly ordered protein aggregates, termed amyloid fibrils, are associated with a broad range of dise...
<p>A. S100 proteins (1 mg/mL) were incubated at pH 2.5 and 37°C during 160 h without agitation in th...
Amyloid-beta fibrils within the human brain have been reported to be a possible cause for Alzheimer’...
<p>(A) Thioflavin T signal versus time of amyloid β peptides. Peptide samples, at 20 µM and containi...
AbstractThe mechanisms linking deposits of insoluble amyloid fibrils to the debilitating neuronal ce...
Amyloidosis is a group of diseases in which amyloid fibrils accumulate and deposit into plaques and ...
The aggregation of proteins into insoluble filamentous amyloid fibrils is a pathological hallmark of...
<p>Kinetics of lysozyme fibril extension in absence and in presence of different concentration of os...