In vitro screening of natural compounds with antitumor activity by trypsin.
- Author:
Jia-Li HE
1
;
Jin-Qiu ZHANG
1
;
Si-Yi WANG
1
;
Zheng ZHANG
1
;
De-Xing ZHANG
1
;
Jun-Qing QIAN
2
,
3
Author Information
1. School of Pharmacy, Zhejiang University of Technology, Hangzhou 310032, China.
2. School of Pharmacy, Zhejiang University of Technology, Hangzhou 310032, China. qjq@zjut.edu.cn
3. 2112007172@zjut.edu.cn.
- Publication Type:Journal Article
- MeSH:
Humans;
Trypsin/chemistry*;
Alkaloids/pharmacology*
- From:
Acta Physiologica Sinica
2022;74(6):1014-1022
- CountryChina
- Language:Chinese
-
Abstract:
In order to investigate the feasibility of in vitro screening the antitumor activity of natural compounds by trypsin, porcine trypsin was used to for screening test, which is marked by inhibition of enzyme activity. Four compounds, namely daidzin, genistin, matrine and oxymatrine, were selected as test subjects. The natural antitumor drug camptothecin was used as the control. The inhibitory effect was detected by two experimental methods: direct detection of trypsin activity inhibition and hydrolysis of bovine serum albumin by trypsin. The results showed the inhibitory effects of the four natural compounds on trypsin, and the inhibition rates of the four natural compounds were significantly different. The enzyme activity assay showed that the inhibitory effect of matrine was better than that of oxymatrine, indicating that trypsin had a good screening resolution. The inhibitory effect was significantly increased with the increased ratio of sample to trypsin, suggesting the structure-activity correlation and dose-effect correlation of the screening methods. Altogether, the experimental method of screening antitumor activity of natural compounds by trypsin has good application values. Since porcine trypsin is similar to human trypsin in terms of molecular structure and performance, it is more applicable for screening of antitumor efficacy of natural pharmacodynamic compounds.
