Literature DB >> 15521811

Protein folding, misfolding, and aggregation. Formation of inclusion bodies and aggresomes.

K A Markossian1, B I Kurganov.   

Abstract

In this review the mechanisms of protein folding, misfolding, and aggregation as well as the mechanisms of cell defense against toxic protein aggregates are considered. Misfolded and aggregated proteins in cells are exposed to chaperone-mediated refolding and are degraded by proteasomes if refolding is impossible. Proteolysis-stable protein aggregates accumulate, forming inclusion bodies. In eucaryotic cells, protein aggregates form structures in the pericentrosomal area that have been termed "aggresomes". Formation of aggresomes in cells is a general cellular response to the presence of misfolded proteins when the degrading capacity of the cells is exceeded. The role of aggresomes in disturbance of the proteasomal system operation and in cellular death, particularly in the so-called "protein conformational diseases", is discussed.

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Year:  2004        PMID: 15521811     DOI: 10.1023/b:biry.0000043539.07961.4c

Source DB:  PubMed          Journal:  Biochemistry (Mosc)        ISSN: 0006-2979            Impact factor:   2.487


  37 in total

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Review 3.  Integration of clearance mechanisms: the proteasome and autophagy.

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4.  Two distinct states of Escherichia coli cells that overexpress recombinant heterogeneous β-galactosidase.

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5.  Study of kinetics of thermal aggregation of mitochondrial aspartate aminotransferase by dynamic light scattering: protective effect of alpha-crystallin.

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Journal:  Eur Biophys J       Date:  2009-01-27       Impact factor: 1.733

Review 6.  E3 ubiquitin ligases in protein quality control mechanism.

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Journal:  Proteomics       Date:  2010-12       Impact factor: 3.984

8.  In vivo crystallization of human IgG in the endoplasmic reticulum of engineered Chinese hamster ovary (CHO) cells.

Authors:  Haruki Hasegawa; John Wendling; Feng He; Egor Trilisky; Riki Stevenson; Heather Franey; Francis Kinderman; Gary Li; Deirdre Murphy Piedmonte; Timothy Osslund; Min Shen; Randal R Ketchem
Journal:  J Biol Chem       Date:  2011-04-04       Impact factor: 5.157

9.  Lewy body-like α-synuclein aggregates resist degradation and impair macroautophagy.

Authors:  Selcuk A Tanik; Christine E Schultheiss; Laura A Volpicelli-Daley; Kurt R Brunden; Virginia M Y Lee
Journal:  J Biol Chem       Date:  2013-03-26       Impact factor: 5.157

10.  Proteasome inhibition rescues clinically significant unstable variants of the mismatch repair protein Msh2.

Authors:  Tim Arlow; Kristan Scott; Aubrey Wagenseller; Alison Gammie
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-17       Impact factor: 11.205

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