Ye Junyi, Huang Yong, Jiang Xuewa, Shen Pingping, Zhang Chaofeng, Zhang Jian
Department of Resources Science of Traditional Chinese Medicines and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Jiangsu Key Laboratory of TCM Evaluation and Translational Research, China Pharmaceutical University, Nanjing, 211198, People's Republic of China.
Chin Med. 2023 Jul 4;18(1):81. doi: 10.1186/s13020-023-00789-7.
High mobility group box 1 protein (HMGB1), a lethal late inflammatory mediator, contributes to the pathogenesis of diverse inflammatory and infectious diseases. Astragaloside IV and calycosin as active ingredients in Astragalus membranaceus, possess potent regulatory ability on HMGB1-induced inflammation, however, the interaction between these two phytochemicals and HMGB1 has not been elucidated yet.
To further investigate the interaction of astragaloside IV, calycosin with HMGB1 protein, surface plasma resonance (SPR) and a series of spectroscopic methods, including UV spectra, fluorescence spectroscopy, circular dichroism (CD), were used. Molecular docking was also carried out to predict the atomic level's binding modes between two components and HMGB1.
Astragaloside IV and calycosin were found to be able to bind HMGB1 directly and affect the secondary structure and environment of the chromogenic amino acids of HMGB1 to different extents. In silico, astragaloside IV and calycosin showed a synergistic effect by binding to the two independent domains B-box and A-box in HMGB1, respectively, where hydrogen and hydrophobicity bonds were regarded as the crucial forces.
These findings showed that the interaction of astragaloside IV and calycosin with HMGB1 impaired its proinflammatory cytokines function, providing a new perspective for understanding the mechanism of A. membranaceus in treating aseptic and infectious diseases.
高迁移率族蛋白B1(HMGB1)是一种致命的晚期炎症介质,在多种炎症和感染性疾病的发病机制中起作用。黄芪甲苷和毛蕊异黄酮作为黄芪中的活性成分,对HMGB1诱导的炎症具有强大的调节能力,然而,这两种植物化学物质与HMGB1之间的相互作用尚未阐明。
为了进一步研究黄芪甲苷、毛蕊异黄酮与HMGB1蛋白的相互作用,采用了表面等离子体共振(SPR)以及一系列光谱方法,包括紫外光谱、荧光光谱、圆二色光谱(CD)。还进行了分子对接以预测两种成分与HMGB1之间原子水平的结合模式。
发现黄芪甲苷和毛蕊异黄酮能够直接结合HMGB1,并不同程度地影响HMGB1发色氨基酸的二级结构和环境。在计算机模拟中,黄芪甲苷和毛蕊异黄酮分别通过与HMGB1中的两个独立结构域B盒和A盒结合而显示出协同作用,其中氢键和疏水键被视为关键作用力。
这些发现表明黄芪甲苷和毛蕊异黄酮与HMGB1的相互作用损害了其促炎细胞因子功能,为理解黄芪治疗无菌性和感染性疾病的机制提供了新的视角。