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基于IgY抗体的免疫分析法用于筛选草药中CYP2E1抑制剂/增强剂的开发。

Development of an IgY Antibody-Based Immunoassay for the Screening of the CYP2E1 Inhibitor/Enhancer from Herbal Medicines.

作者信息

Jiang Zhihui, Jiang Xuemei, Li Cui, Xue Huiting, Zhang Xiaoying

机构信息

College of Veterinary Medicine, Northwest A&F UniversityYangling, China; Chinese-German Joint Laboratory for Natural Product Research, Qinling-Bashan Mountains Bioresources Comprehensive Development C.I.C., College of Biological Science and Engineering, Shaanxi University of TechnologyHanzhong, China.

College of Veterinary Medicine, Northwest A&F University Yangling, China.

出版信息

Front Pharmacol. 2016 Dec 22;7:502. doi: 10.3389/fphar.2016.00502. eCollection 2016.

Abstract

Cytochrome P450 (CYP) 2E1 is an important enzyme involved in the metabolism of many endogenous and exogenous compounds. It is essential to evaluate the expression of CYP2E1 in the studies of drug-drug interactions and the screening of drugs, natural products, and foodstuffs. The present work is a feasibility study on the development of immunoassays using a specific and sensitive chicken-sourced anti-CYP2E1 IgY antibody. Cloning, expression, and purification of a recombinant CYP2E1 (mice origin) protein were carried out. Anti-CYP2E1 IgY antibodies were generated by immunizing white Leghorn chickens with purified recombinant CYP2E1 protein and were purified by immune affinity chromatography. The IgY titer attained a peak level (≥1:128,000) after the fifth booster injection. For evaluation of the expression of CYP2E1 in different herbal treatment samples, the mice were treated by oral gavage for 3 days with alcohol (50% 15 mL/kg), acetaminophen (APAP, 300 mg/kg), extract (100 mg/kg), Alhagi-honey extract (100 mg/kg), extract (100 mg/kg), hyperoside (50 mg/kg), isoquercetin (50 mg/kg), 4-hydroxyphenylacetic acid (50 mg/kg), 3-hydroxyphenylacetic acid (50 mg/kg), and 3,4-hydroxyphenylacetic acid (50 mg/kg). The expression of CYP2E1 was determined by Western blot analysis, immunohistochemistry, ELISA, and immunomagnetic beads (IMBs) using anti-CYP2E1 IgY in liver tissue. The results showed that extract, Alhagi-honey extract, extract, hyperoside, isoquercetin, and their xenobiotics 4-hydroxyphenylacetic acid, 3-hydroxyphenylacetic acid, and 3,4-hydroxyphenylacetic acid significantly decreased CYP2E1 levels. Alcohol and APAP treatments significantly increased CYP2E1 levels as analyzed with Western blot analysis, immunohistochemistry, and ELISA. The IMB method is suitable for large-scale screening, and it is a rapid screening (20 min) that uses a portable magnet and has no professional requirements for the operator, which makes it useful for on-the-spot analysis. Considering these results, the anti-CYP2E1 IgY could be applied as a novel research tool in screening for the CYP2E1 inhibitor/enhancer.

摘要

细胞色素P450(CYP)2E1是一种参与多种内源性和外源性化合物代谢的重要酶。在药物相互作用研究以及药物、天然产物和食品筛选中,评估CYP2E1的表达至关重要。本研究是关于利用特异性和敏感性高的鸡源抗CYP2E1 IgY抗体开发免疫分析方法的可行性研究。进行了重组CYP2E1(小鼠来源)蛋白的克隆、表达和纯化。用纯化的重组CYP2E1蛋白免疫白来航鸡产生抗CYP2E1 IgY抗体,并通过免疫亲和层析进行纯化。在第五次加强注射后,IgY效价达到峰值水平(≥1:128,000)。为了评估不同草药处理样品中CYP2E1的表达,用酒精(50%,15 mL/kg)、对乙酰氨基酚(APAP,300 mg/kg)、[草药名称1]提取物(100 mg/kg)、骆驼刺蜂蜜提取物(100 mg/kg)、[草药名称2]提取物(100 mg/kg)、金丝桃苷(50 mg/kg)、异槲皮苷(50 mg/kg)、4-羟基苯乙酸(50 mg/kg)、3-羟基苯乙酸(50 mg/kg)和3,4-羟基苯乙酸(50 mg/kg)对小鼠进行连续3天的灌胃处理。使用抗CYP2E1 IgY通过蛋白质免疫印迹分析(Western blot analysis)、免疫组织化学、酶联免疫吸附测定(ELISA)和免疫磁珠(IMBs)法测定肝脏组织中CYP2E1的表达。结果表明,[草药名称1]提取物、骆驼刺蜂蜜提取物、[草药名称2]提取物、金丝桃苷、异槲皮苷及其外源性物质4-羟基苯乙酸、3-羟基苯乙酸和3,4-羟基苯乙酸显著降低了CYP2E1水平。蛋白质免疫印迹分析、免疫组织化学和ELISA分析结果显示,酒精和APAP处理显著增加了CYP2E1水平。免疫磁珠法适用于大规模筛选,是一种快速筛选方法(20分钟),使用便携式磁铁,对操作人员无专业要求,适用于现场分析。基于这些结果,抗CYP2E1 IgY可作为一种新型研究工具用于筛选CYP2E1抑制剂/增强剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ef9/5177661/117aa7cc47bd/fphar-07-00502-g001.jpg

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