AbstractThe formation of protein fibrils, and in particular amyloid fibrils, underlies many human diseases. Understanding fibril formation mechanisms is important for understanding disease pathology, but fibril formation kinetics can be complicated, making the relationship between experimental observables and specific mechanisms unclear. Here we examine one often-proposed fibril formation mechanism, nucleated polymerization with off-pathway aggregation. We use the characteristics of this mechanism to derive three tests that can be performed on experimental data to identify it. We also find that this mechanism has an especially striking feature: although increasing protein concentrations generally cause simple nucleated polymerizations to re...
AbstractAmyloid fibrillation has been intensively studied because of its association with various ne...
An abnormal dependence of the rate of amyloid formation on protein concentration has been recently o...
Amyloid fibril formation is central to the etiology of a wide range of serious human diseases, such ...
AbstractThe formation of protein fibrils, and in particular amyloid fibrils, underlies many human di...
AbstractThe formation of amyloid and other types of protein fibrils is thought to proceed by a nucle...
Self-assembly of misfolded proteins into ordered fibrillar aggregates known as amyloid results in nu...
AbstractThe assembly of various proteins into fibrillar aggregates is an important phenomenon with w...
The growth of amyloid fibrils requires a disordered or partially unfolded protein to bind to the fib...
AbstractOne and the same protein can self-assemble into amyloid fibrils with different morphologies....
AbstractThe nucleation-growth model has been used extensively for characterizing in vitro amyloid fi...
The mechanism of amyloid fibril formation by proteins has been classically described by the nucleati...
Proteins possessing very different structures, or even no structure, form amyloid fibrils that are v...
AbstractAmyloid is a highly ordered form of aggregate comprising long, straight and unbranched prote...
One and the same protein can self-assemble into amyloid fibrils with different morphologies. The phe...
Misfolding and accumulation of insoluble protein aggregates in the form of amyloid fibrils is assoc...
AbstractAmyloid fibrillation has been intensively studied because of its association with various ne...
An abnormal dependence of the rate of amyloid formation on protein concentration has been recently o...
Amyloid fibril formation is central to the etiology of a wide range of serious human diseases, such ...
AbstractThe formation of protein fibrils, and in particular amyloid fibrils, underlies many human di...
AbstractThe formation of amyloid and other types of protein fibrils is thought to proceed by a nucle...
Self-assembly of misfolded proteins into ordered fibrillar aggregates known as amyloid results in nu...
AbstractThe assembly of various proteins into fibrillar aggregates is an important phenomenon with w...
The growth of amyloid fibrils requires a disordered or partially unfolded protein to bind to the fib...
AbstractOne and the same protein can self-assemble into amyloid fibrils with different morphologies....
AbstractThe nucleation-growth model has been used extensively for characterizing in vitro amyloid fi...
The mechanism of amyloid fibril formation by proteins has been classically described by the nucleati...
Proteins possessing very different structures, or even no structure, form amyloid fibrils that are v...
AbstractAmyloid is a highly ordered form of aggregate comprising long, straight and unbranched prote...
One and the same protein can self-assemble into amyloid fibrils with different morphologies. The phe...
Misfolding and accumulation of insoluble protein aggregates in the form of amyloid fibrils is assoc...
AbstractAmyloid fibrillation has been intensively studied because of its association with various ne...
An abnormal dependence of the rate of amyloid formation on protein concentration has been recently o...
Amyloid fibril formation is central to the etiology of a wide range of serious human diseases, such ...