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Cell toxicity and conformational disease
- Source :
- Trends in Cell Biology. 15:574-580
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- Numerous disorders, including Alzheimer's, Parkinson's and other late-onset neurodegenerative diseases, arise from the conformationally driven aggregation of individual proteins. Previous focus on just one end-product of such aggregation - extracellular deposits of amyloid - has diverted attention from what is now recognized as being primarily intracellular disease processes. Recent structural findings show how cytotoxicity can result from even minor changes in conformation that do not lead to amyloid formation, as with the accumulation within the endoplasmic reticulum of intact mutant alpha-1-antitrypsin in hepatocytes and of neuroserpin in neurons. Studies in Alzheimer's and other dementias also indicate that the damage occurs at the stage of the initial intermolecular linkages that precede amyloid formation. The challenge now is to determine the detailed mechanisms of this cytotoxicity.
- Subjects :
- Models, Molecular
Amyloid
Protein Folding
Erythrocytes
Protein Conformation
Biology
Endoplasmic Reticulum
Inclusion bodies
Protein structure
Neuroserpin
Extracellular
Animals
Humans
Disease
Serpins
Inclusion Bodies
Cell Death
Liver Diseases
Endoplasmic reticulum
Neuropeptides
Pancreatic Diseases
Proteins
Neurodegenerative Diseases
Cell Biology
Cell biology
Biochemistry
alpha 1-Antitrypsin
Mutation
Dementia
Kidney Diseases
Protein folding
Intracellular
Protein Binding
Subjects
Details
- ISSN :
- 09628924
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Trends in Cell Biology
- Accession number :
- edsair.doi.dedup.....55b7ac7abde4b2f28821226010022251