4.5 Article

Structure-Based Screening Reveals a Ligand That Stabilizes the [2Fe-2S] Clusters of Human mitoNEET and Reduces Ovarian Cancer Cell Proliferation

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 126, Issue 46, Pages 9559-9565

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.2c05728

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Funding

  1. Marie Skodowska-Curie [765048]

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This study identified a new human mitoNEET binding ligand (NTS-01) that specifically binds to the human mNT protein and stabilizes its [2Fe-2S] clusters under oxidative conditions in vitro. Treatment with NTS-01 induces mitochondrial fragmentation and reduces ovarian cancer cell proliferation. The NTS-01 molecule represents a promising lead compound for further drug design studies against ovarian cancer.
Human NEET proteins play an important role in a variety of diseases, including cancer. Using the recently published X-ray structure of the human mNT-M1 complex, we screened a commercial chemical compound library and identified a new human mitoNEET (mNT) binding ligand (NTS-01). Biochemical investigations revealed that NTS-01 specifically binds to the human mNT protein and stabilizes its [2Fe-2S] clusters under oxidative conditions in vitro. Treatment of ovarian cancer cells with NTS-01 induces ovarian cancer (SKOV-3) mitochondrial fragmentation (fission) and reduces ovarian cancer cell proliferation in a 2D single-layer cell culture, as well as in a 3D-spheroids culture. The NTS-01 molecule represents therefore a new lead compound for further drug design studies attempting to develop efficient treatment against ovarian cancer.

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