2. Academic Validation
  3. Structural basis for a Polθ helicase small-molecule inhibitor revealed by cryo-EM

Structural basis for a Polθ helicase small-molecule inhibitor revealed by cryo-EM

  • Nat Commun. 2024 Aug 14;15(1):7003. doi: 10.1038/s41467-024-51351-4.
Fumiaki Ito # 1,  Ziyuan Li # 1,  Leonid Minakhin 2,  Gurushankar Chandramouly 2,  Mrityunjay Tyagi 2,  Robert Betsch 3,  John J Krais 3,  Bernadette Taberi 2,  Umeshkumar Vekariya 4,  Marissa Calbert 2,  Tomasz Skorski 4,  Neil Johnson 3,  Xiaojiang S Chen 5,  Richard T Pomerantz 6
Affiliations

Affiliations

  • 1 Molecular and Computational Biology, Department of Biological Sciences and Chemistry, University of Southern California, Los Angeles, California, CA, 90089, USA.
  • 2 Department of Biochemistry and Molecular Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, 19107, USA.
  • 3 Nuclear Dynamics Program, Fox Chase Cancer Center, Philadelphia, PA, 19111, USA.
  • 4 Fels Cancer Institute for Personalized Medicine, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, 19140, USA.
  • 5 Molecular and Computational Biology, Department of Biological Sciences and Chemistry, University of Southern California, Los Angeles, California, CA, 90089, USA. xiaojiac@usc.edu.
  • 6 Department of Biochemistry and Molecular Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, 19107, USA. richard.pomerantz@jefferson.edu.
  • # Contributed equally.
PMID: 39143110 DOI: 10.1038/s41467-024-51351-4
Abstract

DNA Polymerase theta (Polθ) is a DNA helicase-polymerase protein that facilitates DNA repair and is synthetic lethal with homology-directed repair (HDR) factors. Thus, Polθ is a promising precision oncology drug-target in HDR-deficient cancers. Here, we characterize the binding and mechanism of action of a Polθ helicase (Polθ-hel) small-molecule inhibitor (AB25583) using cryo-EM. AB25583 exhibits 6 nM IC50 against Polθ-hel, selectively kills BRCA1/2-deficient cells, and acts synergistically with olaparib in Cancer cells harboring pathogenic BRCA1/2 mutations. Cryo-EM uncovers predominantly dimeric Polθ-hel:AB25583 complex structures at 3.0-3.2 Å. The structures reveal a binding-pocket deep inside the helicase central-channel, which underscores the high specificity and potency of AB25583. The cryo-EM structures in conjunction with biochemical data indicate that AB25583 inhibits the ATPase activity of Polθ-hel helicase via an allosteric mechanism. These detailed structural data and insights about AB25583 inhibition pave the way for accelerating drug development targeting Polθ-hel in HDR-deficient cancers.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-162859
    Polθ-hel抑制剂
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