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Regulated protein turnover: snapshots of the proteasome in action

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 15, Issue 2, Pages 122-133

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrm3741

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Funding

  1. Gates Foundation
  2. Welch Foundation
  3. US National Institutes of Health [R01 GM63004, R01 GM094479, U54 GM105816, U54 CA143869]

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The ubiquitin proteasome system (UPS) is the main ATP-dependent protein degradation pathway in the cytosol and nucleus of eukaryotic cells. At its centre is the 26S proteasome, which degrades regulatory proteins and misfolded or damaged proteins. In a major breakthrough, several groups have determined high-resolution structures of the entire 26S proteasome particle in different nucleotide conditions and with and without substrate using cryo-electron microscopy combined with other techniques. These structures provide some surprising insights into the functional mechanism of the proteasome and will give invaluable guidance for genetic and biochemical studies of this key regulatory system.

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