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PMID: 20453918 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

CSPalpha: the neuroprotective J protein.

Biochemistry and cell biology = Biochimie et biologie cellulaire ·Vol. 88 ·No. 2 ·2010-04-00 ·Pages 157-65

Johnson JN, Ahrendt E, Braun JE

Abstract

Cysteine string protein (CSPalpha, also called DnaJC5) is unique among J proteins. Similar to other J proteins, CSPalpha interacts with and activates the ATPase of Hsc70s (heat shock proteins of 70 kDa), thereby harnessing the ATPase activity for conformational work on client proteins. In contrast to other J proteins, CSPalpha is anchored to synaptic vesicles, as well as to exocrine, endocrine and neuroendocrine secretory granules, and has been shown to have an essential anti-neurodegenerative role. CSPalpha-null organisms exhibit progressive neurodegeneration, behavioural deficits, and premature death, most likely due to the progressive misfolding of one or more client proteins. Here we highlight recent advances in our understanding of the critical role that CSPalpha plays in governing exocytotic secretory functions.

MeSH Terms
Animals HSP40 Heat-Shock Proteins/chemistry,metabolism HSP70 Heat-Shock Proteins/chemistry,metabolism Humans Membrane Proteins/chemistry,metabolism Sodium-Potassium-Exchanging ATPase/chemistry,metabolism
Chemicals
HSP40 Heat-Shock Proteins HSP70 Heat-Shock Proteins Membrane Proteins cysteine string protein Sodium-Potassium-Exchanging ATPase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Johnson Jadah N
Department of Physiology and Pharmacology and the Hotchkiss Brain Institute, University of Calgary, Calgary, AB T2N 4N1, Canada.
Ahrendt Eva
Braun Janice E A
Article Info
Journal
Biochemistry and cell biology = Biochimie et biologie cellulaire
Abbr.
Biochem Cell Biol
ISSN
1208-6002
Published
2010-04-00
Pages
157-65
Language
English
Region
Canada
NLM ID
8606068
Subset
IM
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