Emerging Mechanistic Insights into AAA Complexes Regulating Proteasomal Degradation

Biomolecules

Friedrich Förster¹  Jan M. Schuller²  Pia Unverdorben² 

[1] Department of Molecular Structural Biology, Max-Planck Institute of Biochemistry, Martinsried D-82152, Germany;

关键词: AAA-ATPases;    26S proteasome;    Cdc48;    p97;    unfoldase;    segregase;    cryo-EM;   

DOI  :  10.3390/biom4030774

来源: mdpi

【 摘 要 】

The 26S proteasome is an integral element of the ubiquitin-proteasome system (UPS) and, as such, responsible for regulated degradation of proteins in eukaryotic cells. It consists of the core particle, which catalyzes the proteolysis of substrates into small peptides, and the regulatory particle, which ensures specificity for a broad range of substrates. The heart of the regulatory particle is an AAA-ATPase unfoldase, which is surrounded by non-ATPase subunits enabling substrate recognition and processing. Cryo-EM-based studies revealed the molecular architecture of the 26S proteasome and its conformational rearrangements, providing insights into substrate recognition, commitment, deubiquitylation and unfolding. The cytosol proteasomal degradation of polyubiquitylated substrates is tuned by various associating cofactors, including deubiquitylating enzymes, ubiquitin ligases, shuttling ubiquitin receptors and the AAA-ATPase Cdc48/p97. Cdc48/p97 and its cofactors function upstream of the 26S proteasome, and their modular organization exhibits some striking analogies to the regulatory particle. In archaea PAN, the closest regulatory particle homolog and Cdc48 even have overlapping functions, underscoring their intricate relationship. Here, we review recent insights into the structure and dynamics of the 26S proteasome and its associated machinery, as well as our current structural knowledge on the Cdc48/p97 and its cofactors that function in the ubiquitin-proteasome system (UPS).

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.