AbstractA theory has been developed that could explain prion infection. Prions could be molecular chaperones that are required for their own assembly. The theory has been deduced from an analysis of protein folding and consequences explored by computer simulations. Thermo-kinetic analysis of protein folding shows that a misfolded chaperone gives rise to new misfolded chaperones. Consequently such a protein could behave as a new kind of informative molecule and replicate misfolding according to a process similar to infection. A quantitative model has been derived from this hypothesis that displays the characteristics of prion infections. This hypothesis satisfactorily explains the three manifestations infection, familial and sporadic — that ...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Protein (and nucleic acid) folding can be viewed as biological morphogenesis at its most elementary ...
The structural conversion of the prion protein PrP into a transmissible, misfolded form is the centr...
Prions are infectious proteins that are responsible for a number of mammalian degenerative disease...
Newly made polypeptide chains not only require the help of molecular chaperones to rapidly reach the...
According to the Koch postulates an infectious organism is the one that can be isolated from an host...
Prions are infectious proteins that cause neurodegenerative diseases called transmissible spongiform...
AbstractThe discovery of prion disease transmission in mammals, as well as a non-Mendelian type of i...
Prion diseases include a group of either sporadic, inherited or infectious disorders characterized b...
Abstract Prions are proteinaceous pathogens responsible for a wide range of neurodegenerative diseas...
International audiencePrions are proteins capable of adopting misfolded conformations and transmitti...
Protein aggregation causes malfunction in several biochemical processes. Genetic and spontaneous for...
Prions are responsible for a heterogeneous group of fatal neurodegenerative diseases, involving post...
Prions are proteins most commonly associated with fatal neurodegenerative diseases in mammals but ar...
Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encode...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Protein (and nucleic acid) folding can be viewed as biological morphogenesis at its most elementary ...
The structural conversion of the prion protein PrP into a transmissible, misfolded form is the centr...
Prions are infectious proteins that are responsible for a number of mammalian degenerative disease...
Newly made polypeptide chains not only require the help of molecular chaperones to rapidly reach the...
According to the Koch postulates an infectious organism is the one that can be isolated from an host...
Prions are infectious proteins that cause neurodegenerative diseases called transmissible spongiform...
AbstractThe discovery of prion disease transmission in mammals, as well as a non-Mendelian type of i...
Prion diseases include a group of either sporadic, inherited or infectious disorders characterized b...
Abstract Prions are proteinaceous pathogens responsible for a wide range of neurodegenerative diseas...
International audiencePrions are proteins capable of adopting misfolded conformations and transmitti...
Protein aggregation causes malfunction in several biochemical processes. Genetic and spontaneous for...
Prions are responsible for a heterogeneous group of fatal neurodegenerative diseases, involving post...
Prions are proteins most commonly associated with fatal neurodegenerative diseases in mammals but ar...
Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encode...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Protein (and nucleic acid) folding can be viewed as biological morphogenesis at its most elementary ...
The structural conversion of the prion protein PrP into a transmissible, misfolded form is the centr...