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Cellular and Molecular Life Sciences: CMLS logoLink to Cellular and Molecular Life Sciences: CMLS
. 2007 Jun 14;64(19-20):2525. doi: 10.1007/s00018-007-7188-6

To be, or not to be — molecular chaperones in protein degradation

V Arndt 1, C Rogon 1, J Höhfeld 1,
PMCID: PMC11136327  PMID: 17565442

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.

Keywords. CHIP, Parkin, Hsp70, Hsp90, ubiquitin, proteasome

Footnotes

Received 16 April 2007; received after revision 10 May 2007; accepted 16 May 2007


Articles from Cellular and Molecular Life Sciences: CMLS are provided here courtesy of Springer

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