Literature DB >> 16170215

Protein misfolding, aggregation, and degradation in disease.

Niels Gregersen1, Lars Bolund, Peter Bross.   

Abstract

Pathologies associated with protein misfolding have been observed in neurodegenerative diseases such as Alzheimer's disease, metabolic diseases like phenylketonuria, and diseases affecting structural proteins like collagen or keratin. Misfolding of mutant proteins in these and many other diseases may result in premature degradation, formation of toxic aggregates, or incorporation of toxic conformations into structures. We review common traits of these diverse diseases under the unifying view of protein misfolding. The molecular pathogenesis is discussed in the context of protein quality control systems consisting of molecular chaperones and intracellular proteases that assist the folding and supervise the maintenance of the folded structure. Furthermore, genetic and environmental factors that may modify the severity of these diseases are underscored.

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Year:  2005        PMID: 16170215     DOI: 10.1385/MB:31:2:141

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  64 in total

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6.  A putative protein-sequestration site involving intermediate filaments for protein degradation by autophagy. Studies with transplanted Sendai-viral envelope proteins in HTC cells.

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Review 2.  Knitting and untying the protein network: modulation of protein ensembles as a therapeutic strategy.

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7.  Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress.

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9.  Lysozyme Mutants Accumulate in Cells while Associated at their N-terminal Alpha-domain with the Endoplasmic Reticulum Chaperone GRP78/BiP.

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