Characterisation of several Hsp70 interacting proteins from mammalian organelles

Naylor, Dean J., Hoogenraad, Nicholas J. and Høj, Peter B. (1999) Characterisation of several Hsp70 interacting proteins from mammalian organelles. Biochimica Et Biophysica Acta-Protein Structure and Molecular Enzymology, 1431 2: 443-450. doi:10.1016/S0167-4838(99)00070-9

Author Naylor, Dean J.
Hoogenraad, Nicholas J.
Høj, Peter B.
Title Characterisation of several Hsp70 interacting proteins from mammalian organelles
Journal name Biochimica Et Biophysica Acta-Protein Structure and Molecular Enzymology
ISSN 0167-4838
Publication date 1999-05-18
Sub-type Article (original research)
DOI 10.1016/S0167-4838(99)00070-9
Volume 1431
Issue 2
Start page 443
End page 450
Total pages 8
Place of publication Amsterdam, Netherlands
Publisher Elsevier
Language eng
Abstract Since both the spectrum and characteristics of in vivo substrates with affinity for Hsp70 members are largely unknown, we have investigated the range and type of mammalian organellar proteins which selectively interact with immobilised Escherichia coli Hsp70 (DnaK). Amongst a subset of organellar proteins selectively retained on DnaK, the major constituents represent unstable proteins and subunits of oligomeric proteins. The interactions with DnaK were diminished in the presence of mt-Hsp70 and BiP, while the complexes formed with DnaK were dissociated in the presence of K+ and GrpE-like co-chaperones, suggesting that these organellar proteins constitute general Hsp70 substrates. Protein sequence analysis identified the major DnaK interacting constituents as the mitochondrial transcription factor A, the α- (but not the β-) subunit of succinyl CoA synthetase, mitochondrial 2,4-dienoyl CoA reductase, endoplasmic reticulum cyclophilin-B, peroxisomal multifunctional enzyme and a previously undescribed peroxisomal protein suspected to represent an isoform of 2,4-dienoyl CoA reductase. The selective retention of these fully synthesised proteins on Hsp70 most likely reflects the function of this molecular chaperone in protein biogenesis, but additionally, could extend the known functions of Hsp70 to include modulating the activities of certain proteins or enzymes which are important in cellular homeostasis.
Keyword DnaK
Heat shock protein
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: Office of the Vice-Chancellor
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Created: Mon, 26 Aug 2013, 17:06:23 EST by Anthony Yeates on behalf of Office of the Vice-Chancellor