AI-based Virtual Screening of Traditional Chinese Medicine and the Discovery of Novel Inhibitors of TCTP

Author:

Bai Juxia1ORCID,Ni Yangyang1,Zhang Yuqi1,Wan Junfeng1,Liang Liqun1,Qiao Haoran1,Zhu Yanyan1,Zhao Qingjie2,Li Huiyu1ORCID

Affiliation:

1. College of Mathematics and Physics, Shanghai University of Electric Power, Shanghai 201306, China

2. Shanghai Frontiers Science Center for TCM Chemical Biology, Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China

Abstract

Background: Translationally controlled tumour protein (TCTP) is associated with tumor diseases, such as breast cancer, and its inhibitor can reduce the growth of tumor cells. Unfortunately, there is currently no effective medication available for treating TCTP-related breast cancer. Objective: The objective of this study was to explore the inhibitor candidates among natural compounds for the treatment of breast cancer related to TCTP protein. Methods: To explore the potential inhibitors of TCTP, we first screened out four potential inhibitors in the Traditional Chinese Medicine (TCM) for cancer based on AI virtual screening using the docking method, and then revealed the interaction mechanism of TCTP and four candidate inhibitors from TCM with molecular docking and molecular dynamics (MD) methods. method: To explore the potential inhibitors of TCTP, we firstly screened out four potential inhibitors in the major agent of the traditional Chinese herbal medicines (TCMs) for cancer based on AI Virtual Screening using the Docking method, and then revealed the interaction mechanism of TCTP and four candidate inhibitors from TCMs with molecular docking and molecular dynamics (MD) methods. Results: Based on the conformational characteristics and the MD properties of the four leading compounds, we designed the new skeleton molecules with the AI method using MolAICal software. Our MD simulations have revealed that different small molecules bind to different sites of TCTP, but the flexible regions and the signaling pathways are almost the same, and the VDW and hydrophobic interactions are crucial in the interactions between TCTP and ligands. result: Based on the conformational characteristics and the MD properties of the four leading compounds, we designed the new skeleton molecules with AI method using MolAICal software. Our MD simulations reveal that different small molecules bind to different sites of TCTP, but the flexible regions and the signaling pathways are almost the same, the VDW and hydrophobic interactions play important roles in the interactions between ligands and TCTP. Conclusion: We have proposed the candidate inhibitor of TCTP. Our study has provided a potential new method for exploring inhibitors from Traditional Chinese Medicine (TCM).

Publisher

Bentham Science Publishers Ltd.

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