(Q38113990)

29 August 2017

Disulfide bonds in amyloidogenesis diseases related proteins (English)

1 reference

29 August 2017

Yang Li

1

1 reference

29 August 2017

Juan Yan

series ordinal

2

1 reference

29 August 2017

Xin Zhang

series ordinal

3

1 reference

29 August 2017

Kun Huang

series ordinal

4

1 reference

29 August 2017

language of work or name

English

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publication date

19 August 2013

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29 August 2017

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29 August 2017

81

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29 August 2017

11

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29 August 2017

1862-1873

1 reference

Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution

29 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Conformational constraints for amyloid fibrillation: the importance of being unfolded

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Alzheimer's disease: the amyloid cascade hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

21 January 2018

Prion Protein Biology

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Prognostic impact of serum calcitonin and carcinoembryonic antigen doubling-times in patients with medullary thyroid carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Abnormal tau-containing filaments in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Human lysozyme gene mutations cause hereditary systemic amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Amyloid fibrils in human insulinoma and islets of Langerhans of the diabetic cat are derived from a neuropeptide-like protein also present in normal islet cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Toward understanding insulin fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Systemic amyloid deposits in familial British dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Fibril in senile systemic amyloidosis is derived from normal transthyretin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Histological prevalence of beta 2-microglobulin amyloidosis in hemodialysis: a prospective post-mortem study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Toxicity of non-abeta component of Alzheimer's disease amyloid, and N-terminal fragments thereof, correlates to formation of beta-sheet structure and fibrils.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Atrial amyloidosis: an arrhythmogenic substrate for persistent atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Common core structure of amyloid fibrils by synchrotron X-ray diffraction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Protofibrils, pores, fibrils, and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Protein folding and misfolding

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Cryo-electron microscopy structure of an SH3 amyloid fibril and model of the molecular packing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Alzheimer's amyloid fibrils: structure and assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Designing conditions for in vitro formation of amyloid protofilaments and fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Rationalization of the effects of mutations on peptide and protein aggregation rates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Disulfide bonds reduce the toxicity of the amyloid fibrils formed by an extracellular protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Effects of dithiothreitol on the amyloid fibrillogenesis of hen egg-white lysozyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Cellular membrane disruption by amyloid fibrils involved intermolecular disulfide cross-linking.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Promotion of insulin aggregation by protein disulfide isomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The role of thiols and disulfides on protein stability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The alternative conformations of amyloidogenic proteins and their multi-step assembly pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Protein misfolding, evolution and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Amyloid fibrillogenesis: themes and variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Disulfide bonds and protein folding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Volume changes on protein folding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Novel therapeutic strategies for the treatment of protein-misfolding diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Metal-free superoxide dismutase forms soluble oligomers under physiological conditions: a possible general mechanism for familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

HLA-B27 misfolding is associated with aberrant intermolecular disulfide bond formation (dimerization) in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Disulfide bond mediates aggregation, toxicity, and ubiquitylation of familial amyotrophic lateral sclerosis-linked mutant SOD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

NMR solution structure of the human prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

In vitro generation of infectious scrapie prions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Synthetic mammalian prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Thiol-disulfide interchange a potential key to conformational change associated with amyloid fibril formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

A role for intermolecular disulfide bonds in prion diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

In vitro amplification of protease-resistant prion protein requires free sulfhydryl groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Modulation of prion protein structure by pressure and temperature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The role of dimerization in prion replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Structural changes of the prion protein in lipid membranes leading to aggregation and fibrillization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Binding of prion protein to lipid membranes and implications for prion conversion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

NMR structure of the mouse prion protein domain PrP(121-231)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Thioredoxin converts the Syrian hamster (29-231) recombinant prion protein to an insoluble form

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Disulfide bond as a structural determinant of prion protein membrane insertion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Mechanistic studies of the folding of human lysozyme and the origin of amyloidogenic behavior in its disease-related variants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

A kinetic study of the competition between renaturation and aggregation during the refolding of denatured-reduced egg white lysozyme.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Native disulfide bonds greatly accelerate secondary structure formation in the folding of lysozyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Prevention of thermal inactivation and aggregation of lysozyme by polyamines

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

How do surfactants and DTT affect the size, dynamics, activity and growth of soluble lysozyme aggregates?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Amyloid fibrillation of hen egg-white lysozyme is inhibited by TCEP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Destabilization of apoprotein is insufficient to explain Cu,Zn-superoxide dismutase-linked ALS pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Loss of metal ions, disulfide reduction and mutations related to familial ALS promote formation of amyloid-like aggregates from superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Human SOD1 before harboring the catalytic metal: solution structure of copper-depleted, disulfide-reduced form

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Initiation and elongation in fibrillation of ALS-linked superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Activation of superoxide dismutases: putting the metal to the pedal

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Complete loss of post-translational modifications triggers fibrillar aggregation of SOD1 in the familial form of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Posttranslational modifications in Cu,Zn-superoxide dismutase and mutations associated with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

A limited role for disulfide cross-linking in the aggregation of mutant SOD1 linked to familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Disulfide bridges remain intact while native insulin converts into amyloid fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Structure of a protein in a kinetic trap

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Mapping the functional surface of insulin by design: structure and function of a novel A-chain analogue

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The protofilament structure of insulin amyloid fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Independent heterologous fibrillation of insulin and its B-chain peptide

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Islet amyloid and type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Molecular and functional characterization of amylin, a peptide associated with type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Islet amyloid polypeptide inhibits glucagon release and exerts a dual action on insulin release from isolated islets

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Inhibition of central amylin signaling increases food intake and body adiposity in rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The parallel superpleated beta-structure as a model for amyloid fibrils of human amylin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Peptide conformation and supramolecular organization in amylin fibrils: constraints from solid-state NMR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Prediction of aggregation-prone regions in structured proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Contribution of the intrinsic disulfide to the assembly mechanism of islet amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Amylin proprotein processing generates progressively more amyloidogenic peptides that initially sample the helical state

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Effect of the disulfide bond on the monomeric structure of human amylin studied by combined Hamiltonian and temperature replica exchange molecular dynamics simulations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Evidence for a partially structured state of the amylin monomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Formation of disulfide bonds in proteins and peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

A disulfide-linked amyloid-beta peptide dimer forms a protofibril-like oligomer through a distinct pathway from amyloid fibril formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Tyrosine-to-cysteine modification of human alpha-synuclein enhances protein aggregation and cellular toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The clustering and spatial arrangement of beta-sheet sequence, but not order, govern alpha-synuclein fibrillogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Disulfide bond formation and its impact on the biological activity and stability of recombinant therapeutic proteins produced by Escherichia coli expression system

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

What can disulfide bonds tell us about protein energetics, function and folding: simulations and bioninformatics analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Neurodegenerative disease: amyloid pores from pathogenic mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Scanning cysteine mutagenesis analysis of Abeta-(1-40) amyloid fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Experimental constraints on quaternary structure in Alzheimer's beta-amyloid fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Alzheimer beta-amyloid homodimers facilitate A beta fibrillization and the generation of conformational antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

An intersheet packing interaction in A beta fibrils mapped by disulfide cross-linking

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Stabilization of neurotoxic Alzheimer amyloid-beta oligomers by protein engineering

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Alpha-synuclein misfolding and neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Lipid binding inhibits alpha-synuclein fibril formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Role of different regions of alpha-synuclein in the assembly of fibrils.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Release of long-range tertiary interactions potentiates aggregation of natively unstructured alpha-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Trimethylamine-N-oxide-induced folding of alpha-synuclein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Effect of familial Parkinson's disease point mutations A30P and A53T on the structural properties, aggregation, and fibrillation of human alpha-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Conformational behavior of human alpha-synuclein is modulated by familial Parkinson's disease point mutations A30P and A53T.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

Conformational behavior and aggregation of alpha-synuclein in organic solvents: modeling the effects of membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

The Component Polypeptide Chains of Bovine Insulin Nucleate or Inhibit Aggregation of the Parent Protein in a Conformation-dependent Manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPROT.24338

21 January 2018

Identifiers

DOI

10.1002/PROT.24338

1 reference

29 August 2017

1 reference