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抗登革病毒蛋白NS5及穿心莲中穿心莲内酯的抗菌功效:计算机模拟方法

Anti-dengue Viral Protein NS5 and Antibacterial Efficacy of Andrographolide from Andrographis paniculata: An In Silico Approach.

作者信息

Selvam Kandasamy, Sudhakar Chinnappan, Ragu Prasath Arunagiri, Senbagam Duraisamy, Almuhayawi Mohammed S, Alruhaili Mohammed H, Nagshabandi Mohammed K, Selim Samy

机构信息

Department of Biotechnology, Mahendra Arts and Science College (Autonomous), Tamil Nadu, Kalippatti, Namakkal, 637 501, India.

Department of Biomaterials, Saveetha Dental College and Hospitals, SIMATS, Saveetha University, Tamil Nadu, Chennai, 600 077, India.

出版信息

Appl Biochem Biotechnol. 2025 Feb 19. doi: 10.1007/s12010-025-05191-7.

Abstract

The current study examines the anti-dengue and antibacterial potential and in silico drug development of the andrographolide against the pathogens Staphylococcus aureus (1JIJ) and Pseudomonas aeruginosa (6MVN) and the dengue viral protein NS5. The phytochemical analysis identified the presence of flavonoids, alkaloids, saponins, tannins, phenols, glycosides, and steroids in the Andrographis paniculata methanolic leaf extract. Based on the GC-MS analysis, andrographolide was identified as the primary chemical constituent of the medicinal plant A. paniculata and the compound with the largest peak area among other compounds. The agar well diffusion method was employed to observe the antibacterial potential of the methanolic leaf extract against S. aureus and P. aeruginosa. The maximal inhibition zones were 15.6 ± 0.34 mm and 11.7 ± 0.42 mm, respectively. Additionally, andrographolide was docked with the NS5 viral protein and bacterial proteins, including S. aureus TyrRS (PDB: 1JIJ) and P. aeruginosa LasR PDB (ID: 6MVN), resulting in a docking score of - 20.7384 kJ/mol, - 15.0969 kJ/mol, and - 11.1171 kJ/mol, respectively. In summary, our molecular docking experiments with the identified andrographolide compound demonstrated its potential as a drug with anti-dengue viral and antibacterial properties.

摘要

本研究考察了穿心莲内酯对金黄色葡萄球菌(1JIJ)、铜绿假单胞菌(6MVN)以及登革病毒蛋白NS5的抗登革热和抗菌潜力及计算机辅助药物开发。植物化学分析表明穿心莲甲醇叶提取物中存在黄酮类、生物碱、皂苷、单宁、酚类、糖苷和甾体。基于气相色谱-质谱分析,穿心莲内酯被鉴定为药用植物穿心莲的主要化学成分,且在其他化合物中峰面积最大。采用琼脂孔扩散法观察甲醇叶提取物对金黄色葡萄球菌和铜绿假单胞菌的抗菌潜力。最大抑菌圈分别为15.6±0.34毫米和11.7±0.42毫米。此外,穿心莲内酯与NS5病毒蛋白以及细菌蛋白进行对接,包括金黄色葡萄球菌酪氨酰-tRNA合成酶(PDB:1JIJ)和铜绿假单胞菌LasR(PDB ID:6MVN),对接得分分别为-20.7384 kJ/mol、-15.0969 kJ/mol和-11.1171 kJ/mol。总之,我们对鉴定出的穿心莲内酯化合物进行的分子对接实验表明其具有作为抗登革热病毒和抗菌药物的潜力。

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