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A dual-labeling molecule for efficient drug discovery of mitochondrial-lysosomal interactions.
Wu, Jinfang; Wang, Xiaolei; Li, Xiang; Zhu, Zixuan; Cui, Zhongcheng; Zhang, Tao; Zou, Weiwei; Han, Guanying.
Afiliação
  • Wu J; College of Pharmacy, Jinzhou Medical University, Jinzhou, China.
  • Wang X; Reproductive Medicine Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China; NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract (Anhui Medical University), Hefei, Anhui, China; Key Laboratory of Population
  • Li X; College of Pharmacy, Jinzhou Medical University, Jinzhou, China.
  • Zhu Z; College of Pharmacy, Jinzhou Medical University, Jinzhou, China.
  • Cui Z; College of Pharmacy, Jinzhou Medical University, Jinzhou, China.
  • Zhang T; Department of General Surgery, The First Hospital Affiliated with Shandong First Medical University, Jinan, Shandong, China. Electronic address: zhangtao_qdzt@126.com.
  • Zou W; Reproductive Medicine Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China; NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract (Anhui Medical University), Hefei, Anhui, China; Key Laboratory of Population
  • Han G; Medical College of Jinzhou Medical University, Jinzhou, China; The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China. Electronic address: hgy19800223@163.com.
Mol Cell Probes ; 76: 101968, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38960210
ABSTRACT
The close association between organelle interactions, such as mitochondrial-lysosomal interactions, and various diseases, including tumors, remains a challenge for drug discovering and identification. Conventional evaluation methods are often complex and multistep labeling procedures often generate false positives, such as cell damage. To overcome these limitations, we employed a single dual-color reporting molecule called Coupa, which labels mitochondria and lysosomes as blue and red, respectively. This facilitates the evaluation and discovering of drugs targeting mitochondria-lysosome contact (MLC). Using Coupa, we validated the effectiveness of various known antitumor drugs in intervening MLC by assessing their effect on key aspects, such as status, localization, and quantity. This provides evidence for the accuracy and applicability of our dual-color reporting molecule. Notably, we observed that several structural isomers of drugs, including Urolithin (A/B/C), exhibited distinct effects on MLC. In addition, Verteporfin and TEAD were found to induce anti-tumor effects by controlling MLC at the organelle level, suggesting a potential new mechanism of action. Collectively, Coupa offers a novel scientific tool for discovering drugs that target mitochondrial-lysosomal interactions. It not only distinguished the differential effects of structurally similar drugs on the same target, but also reveals new mechanisms underlying the reported antitumor properties of existing drugs. Ultimately, our findings contribute to the advancement of drug discovery and provide valuable insights into the complex interactions between organelles in a disease context.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Descoberta de Drogas / Lisossomos / Mitocôndrias Limite: Humans Idioma: En Revista: Mol Cell Probes Assunto da revista: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Descoberta de Drogas / Lisossomos / Mitocôndrias Limite: Humans Idioma: En Revista: Mol Cell Probes Assunto da revista: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China