The investigation of the interaction determination between carbendazim and elastase, using both in vitro and in silico methods

被引:0
|
作者
Abdollahi-Najafabadi, Mahboubeh [1 ]
Farhadian, Sadegh [1 ,2 ]
Shareghi, Behzad [1 ,2 ]
Asgharzadeh, Sanaz [1 ,2 ]
机构
[1] Shahrekord Univ, Fac Sci, Dept Biol, POB 115, Shahrekord, Iran
[2] Shahrekord Univ, Cent Lab, Shahrekord, Iran
关键词
Pesticides; Carbendazim; Elastase; Molecular simulation; HUMAN HOLO-TRANSFERRIN; BOVINE SERUM-ALBUMIN; INDUCED IMMUNOTOXICITY; SILVER NANOPARTICLES; BETA-LACTOGLOBULIN; PESTICIDE-RESIDUES; BINDING MECHANISM; LIVER; FUNGICIDE; DOCKING;
D O I
10.1016/j.saa.2024.124586
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Pesticides, including fungicides, are one of the important groups of environmental toxins that affect human and animal health. Studies have shown that these compounds are considered chemical pollutants. Carbendazim is a systemic fungicide. Unfortunately, excessive use of carbendazim has caused environmental pollution all over the world. In this study, the effect of carbendazim on the enzyme elastase (secreted from the endocrine gland of the pancreas) has been investigated. In a study, the performance and reaction of carbendazim with elastase were investigated using spectroscopic techniques. The stability and structure of elastase enzymes were studied under the influence of carbendazim. The results of fluorescence emission and UV - visible absorption spectrum showed that in the presence of carbendazim, there is an increase in UV - Vis absorption and a decrease in the intensity of the intrinsic fluorescence emission in the protein spectrum. Additionally, a decrease in the thermal stability of elastase was observed in the presence of carbendazim. The stability and structure of elastase enzyme were investigated in the presence of carbendazim. The results revealed that the UV - Vis absorption increased due to the presence of carbendazim, as indicated by the hyperchromic spectrum at 220 and 280 nm peaks. Additionally, the intrinsic fluorescence emission in the protein spectrum decreased with increasing carbendazim concentration at three different temperatures (298, 303, and 313 K). Moreover, the study demonstrated that the TM decreased from 2.59 to 4.58 with the increase of carbendazim, suggesting a decrease in the stability of the elastase structure in response to the elevated carbendazim concentration. According to the results of the research, the interaction between elastase and carbendazim has occurred, and changes have been made in the enzyme under the influence of carbendazim. The formation of the complex between elastase and carbendazim was consistent with the results obtained from molecular simulation and confirmed the thermodynamic data.
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页数:9
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