Literature DB >> 17565442

To be, or not to be--molecular chaperones in protein degradation.

V Arndt1, C Rogon, J Höhfeld.   

Abstract

To be, or not to be--that is the question not only for Hamlet in Shakespeare's drama but also for a protein associated with molecular chaperones. While long viewed exclusively as cellular folding factors, molecular chaperones recently emerged as active participants in protein degradation. This places chaperones at the center of a life or death decision during protein triage. Here we highlight molecular mechanisms that underlie chaperone action at the folding/degradation interface in mammalian cells. We discuss the importance of chaperone-assisted degradation for the regulation of cellular processes and its emerging role as a target for therapeutic intervention in cancer and amyloid diseases.

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Year:  2007        PMID: 17565442     DOI: 10.1007/s00018-007-7188-6

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  75 in total

Review 1.  Hold me tight: Role of the heat shock protein family of chaperones in cardiac disease.

Authors:  Monte S Willis; Cam Patterson
Journal:  Circulation       Date:  2010-10-26       Impact factor: 29.690

Review 2.  Protein folding in the cytoplasm and the heat shock response.

Authors:  R Martin Vabulas; Swasti Raychaudhuri; Manajit Hayer-Hartl; F Ulrich Hartl
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-12       Impact factor: 10.005

3.  Peroxiredoxin chaperone activity is critical for protein homeostasis in zinc-deficient yeast.

Authors:  Colin W MacDiarmid; Janet Taggart; Kittikhun Kerdsomboon; Michael Kubisiak; Supawee Panascharoen; Katherine Schelble; David J Eide
Journal:  J Biol Chem       Date:  2013-09-10       Impact factor: 5.157

4.  Cytosolic chaperones influence the fate of a toxin dislocated from the endoplasmic reticulum.

Authors:  Robert A Spooner; Philip J Hart; Jonathan P Cook; Paola Pietroni; Christian Rogon; Jörg Höhfeld; Lynne M Roberts; J Michael Lord
Journal:  Proc Natl Acad Sci U S A       Date:  2008-11-06       Impact factor: 11.205

Review 5.  Functions of the Hsp90 chaperone system: lifting client proteins to new heights.

Authors:  Julia M Eckl; Klaus Richter
Journal:  Int J Biochem Mol Biol       Date:  2013-12-15

Review 6.  Molecular chaperones in protein folding and proteostasis.

Authors:  F Ulrich Hartl; Andreas Bracher; Manajit Hayer-Hartl
Journal:  Nature       Date:  2011-07-20       Impact factor: 49.962

Review 7.  Cellular strategies of protein quality control.

Authors:  Bryan Chen; Marco Retzlaff; Thomas Roos; Judith Frydman
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-08-01       Impact factor: 10.005

Review 8.  Molecular chaperones and regulation of tau quality control: strategies for drug discovery in tauopathies.

Authors:  Yoshinari Miyata; John Koren; Janine Kiray; Chad A Dickey; Jason E Gestwicki
Journal:  Future Med Chem       Date:  2011-09       Impact factor: 3.808

9.  UBL/BAG-domain co-chaperones cause cellular stress upon overexpression through constitutive activation of Hsf1.

Authors:  Esben G Poulsen; Caroline Kampmeyer; Franziska Kriegenburg; Jens V Johansen; Kay Hofmann; Christian Holmberg; Rasmus Hartmann-Petersen
Journal:  Cell Stress Chaperones       Date:  2016-12-14       Impact factor: 3.667

10.  Ubr1 and Ubr2 function in a quality control pathway for degradation of unfolded cytosolic proteins.

Authors:  Nadinath B Nillegoda; Maria A Theodoraki; Atin K Mandal; Katie J Mayo; Hong Yu Ren; Rasheda Sultana; Kenneth Wu; Jill Johnson; Douglas M Cyr; Avrom J Caplan
Journal:  Mol Biol Cell       Date:  2010-05-12       Impact factor: 4.138

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