<p>Fibril formation of human prion protein in the absence and in the presence of Ficoll 70 (A) and Ficoll 400 (B), respectively, monitored by ThT fluorescence. The empirical Hill equation was fitted to the data and the solid lines represented the best fit. The final concentration of human PrP was 10 µM. The crowding agent concentrations were 0 (open square), 50 g/l (solid square), 100 g/l (solid circle), 150 g/l (solid triangle), and 200 g/l (inverted solid triangle), respectively. The human PrP was denatured in PBS buffer (pH 7.0) containing 2 M GdnHCl. The assays were carried out at 37°C.</p
Protein aggregation leading to the formation of amyloid fibrils is involved in several neu...
<p>Filament formation of human Tau fragment Tau<sub>244–372</sub> in the absence and in the presence...
The conversion of the alpha-helical, cellular isoform of the prion protein (PrP(C)) to the insoluble...
<p>Fibril formation of pathogenic mutant E196K in the absence and in the presence of Ficoll 70 (A) a...
<p>Human chimera (A and B) and rabbit chimera (C and D) in the absence and presence of Ficoll 70 (A ...
<p>Aggregation of rabbit prion protein in the absence and in the presence of Ficoll 70 (A), dextran ...
Amyloid fibrils associated with neurodegenerative diseases can be considered biologically relevant f...
<div><h3>Background</h3><p>Amyloid fibrils associated with neurodegenerative diseases can be conside...
<p>Transmission electron micrographs of human PrP-H2H3 (A) and rabbit PrP-H2H3 (B) were made after i...
Abstract: Prion diseases and prion- like protein misfolding diseases are related to the accumulation...
Amyloidogenesis of prion protein (PrP) is closely associated with the pathobiology of prion diseases...
Prion diseases and prion-like protein misfolding diseases are related to the accumulation of abnorma...
<p>Results from three independent measurements (denoted by closed square, ▪; closed circle, • and cl...
<p>A) Concentration dependence of prion protein for <i>de novo</i> amyloid formation. Different conc...
<div><p>Background</p><p>It is known that <i>in vivo</i> human prion protein (PrP) have the tendency...
Protein aggregation leading to the formation of amyloid fibrils is involved in several neu...
<p>Filament formation of human Tau fragment Tau<sub>244–372</sub> in the absence and in the presence...
The conversion of the alpha-helical, cellular isoform of the prion protein (PrP(C)) to the insoluble...
<p>Fibril formation of pathogenic mutant E196K in the absence and in the presence of Ficoll 70 (A) a...
<p>Human chimera (A and B) and rabbit chimera (C and D) in the absence and presence of Ficoll 70 (A ...
<p>Aggregation of rabbit prion protein in the absence and in the presence of Ficoll 70 (A), dextran ...
Amyloid fibrils associated with neurodegenerative diseases can be considered biologically relevant f...
<div><h3>Background</h3><p>Amyloid fibrils associated with neurodegenerative diseases can be conside...
<p>Transmission electron micrographs of human PrP-H2H3 (A) and rabbit PrP-H2H3 (B) were made after i...
Abstract: Prion diseases and prion- like protein misfolding diseases are related to the accumulation...
Amyloidogenesis of prion protein (PrP) is closely associated with the pathobiology of prion diseases...
Prion diseases and prion-like protein misfolding diseases are related to the accumulation of abnorma...
<p>Results from three independent measurements (denoted by closed square, ▪; closed circle, • and cl...
<p>A) Concentration dependence of prion protein for <i>de novo</i> amyloid formation. Different conc...
<div><p>Background</p><p>It is known that <i>in vivo</i> human prion protein (PrP) have the tendency...
Protein aggregation leading to the formation of amyloid fibrils is involved in several neu...
<p>Filament formation of human Tau fragment Tau<sub>244–372</sub> in the absence and in the presence...
The conversion of the alpha-helical, cellular isoform of the prion protein (PrP(C)) to the insoluble...