1. Probing hot spots of protein-protein interactions mediated by the safety-belt region of REV7.
- Author
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Dash RC, Arianna GA, Patel SM, Rizzo AA, Harrahill NJ, Korzhnev DM, and Hadden MK
- Subjects
- Humans, Binding Sites, DNA-Binding Proteins metabolism, DNA-Binding Proteins chemistry, DNA-Binding Proteins genetics, Protein Interaction Domains and Motifs, Models, Molecular, Mad2 Proteins metabolism, Mad2 Proteins chemistry, Mad2 Proteins genetics, Protein Binding, DNA-Directed DNA Polymerase metabolism, DNA-Directed DNA Polymerase chemistry
- Abstract
REV7 is a HORMA (Hop1, Rev7, Mad2) family adaptor protein best known as an accessory subunit of the translesion synthesis (TLS) DNA polymerase ζ (Polζ). In this role, REV7 binds REV3, the catalytic subunit of Polζ, by locking REV7-binding motifs (RBMs) in REV3 underneath the REV7 safety-belt loop. The same mechanism is used by REV7 to interact with RBMs from other proteins in DNA damage response (DDR) and mitosis. Because of the importance of REV7 for TLS and other DDR pathways, targeting REV7:RBM protein-protein interactions (PPIs) with small molecules has emerged as a strategy to enhance cancer response to genotoxic chemotherapy. To identify druggable pockets at the REV7:RBM interface, we performed computational analyses of REV7 complexed with several RBM partners. The contributions of different interface regions to REV7:RBM stabilization were corroborated experimentally. These studies provide insights into key intermolecular interactions and establish targetable regions of REV7 for the design of REV7:RBM PPI inhibitors., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Published
- 2024
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