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Folding for the Synapse

  • Book
  • © 2011

Overview

  • Introduces important concepts of folding machineries.

  • Gives examples of the biological relevance of further chaperone functions.

  • Addresses the current view on how protein folding and misfolding contribute to synapse function and dysfunction.

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Table of contents (15 chapters)

  1. The Regulation of Protein (mis)folding, Aggregation and Degradation of Proteins by Molecular Chaperones

  2. Folding for the Synapse

  3. The regulation of protein (mis)folding, aggregation and degradation of proteins by molecular chaperones

  4. The Making of the Synapse: Transport of Proteins, Vesicles and Organelles

  5. Chaperone modalities and homeostatic mechanisms in the synaptic compartment

  6. Chronic neurodegeneration associated with protein misfolding and synaptic dysfunction

About this book

Folding for the Synapse addresses the current view on how protein folding and misfolding, controlled by molecular chaperones, contribute to synapse function and dysfunction. Molecular chaperones have been studied in relation to de novo protein folding, but there is increasing awareness that chaperone function is required for the regulation of protein dynamics when functioning physiologically as an isolated moiety or part of a protein complex. This book will introduce both important concepts of folding machineries and give examples of the biological relevance of further chaperone functions.

Editors and Affiliations

  • School of Biological Sciences, University of Southampton, Southampton, United Kingdom

    Andreas Wyttenbach, Vincent O'Connor

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