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Targeting of client proteins to the VCP/p97/Cdc48 unfolding machine. | LitMetric

Targeting of client proteins to the VCP/p97/Cdc48 unfolding machine.

Front Mol Biosci

Center of Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Essen, Germany.

Published: February 2023

AI Article Synopsis

  • The AAA+ ATPase p97 is a key protein that helps unfold and degrade various client proteins essential for maintaining cell functions.
  • The review discusses how different types of adapters, like Ufd1-Npl4 and SEP-domain adapters, recruit these client proteins to p97 for processing, either through ubiquitylation or independently of it.
  • Both pathways lead to the same outcome by moving the client proteins into p97's central channel, where they undergo unfolding and disassembly, affecting a range of cellular processes.

Article Abstract

The AAA+ ATPase p97 (also called VCP or Cdc48) is a major protein unfolding machine with hundreds of clients in diverse cellular pathways that are critical for cell homeostasis, proliferation and signaling. In this review, we summarize recent advances in understanding how diverse client proteins are targeted to the p97 machine to facilitate client degradation or to strip clients from binding partners for regulation. We describe an elaborate system that is governed by at least two types of alternative adapters. The Ufd1-Npl4 adapter along with accessory adapters targets ubiquitylated clients in the majority of pathways and uses ubiquitin as a universal unfolding tag. In contrast, the family of SEP-domain adapters such as p37 can target clients directly to p97 in a ubiquitin-independent manner. Despite the different targeting strategies, both pathways converge by inserting the client into the p97 pore to initiate a peptide threading mechanism through the central channel of p97 that drives client protein unfolding, protein extraction from membranes and protein complex disassembly processes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941556PMC
http://dx.doi.org/10.3389/fmolb.2023.1142989DOI Listing

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