Molecular properties of complexes formed between the prion protein and synthetic peptides. (Q46007757)

18 December 2017

title

Molecular properties of complexes formed between the prion protein and synthetic peptides. (English)

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18 December 2017

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8

Prusiner SB

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6

Cohen FE

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18 December 2017

Kaneko K

1

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Wille H

2

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18 December 2017

Mehlhorn I

3

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18 December 2017

Zhang H

4

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Ball H

5

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Baldwin MA

7

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language of work or name

English

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publication date

1 July 1997

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18 December 2017

Journal of Molecular Biology

published in

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18 December 2017

volume

270

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issue

4

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page(s)

574-586

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18 December 2017

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

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Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

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Scrapie prions aggregate to form amyloid-like birefringent rods

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Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

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Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

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Measurement of the scrapie agent using an incubation time interval assay

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Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

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Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid

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Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems

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Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

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Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

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Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein

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Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform

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Conformational transitions in peptides containing two putative alpha-helices of the prion protein.

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Unconventional Viruses and the Origin and Disappearance of Kuru

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Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

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https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Linkage of prion protein and scrapie incubation time genes

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

High-level expression and characterization of a purified 142-residue polypeptide of the prion protein

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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11 October 2022

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The relation of the properties of Congo red-stained amyloid fibrils to the -conformation

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Comparison of scrapie and transmissible mink encephalopathy in hamsters. II. Clinical signs, pathology, and pathogenesis

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Prionics or the kinetic basis of prion diseases

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

A new variant of Creutzfeldt-Jakob disease in the UK.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Structural clues to prion replication

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Thermal stability and conformational transitions of scrapie amyloid (prion) protein correlate with infectivity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Physical studies of conformational plasticity in a recombinant prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Molecular biology of prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/JMBI.1997.1135

Identifiers

DOI

10.1006/JMBI.1997.1135

1 reference

18 December 2017

PubMed ID

9245588

1 reference

18 December 2017