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暴露于植物提取物并进行药物筛选后,Fab酶(Fab I和Fab Z)的表达。

Expression of the Fab enzymes (Fab I and Fab Z) from after exposure to plant extracts and drugs screening.

作者信息

Kane Ndeye Fatou, Kyama Mutinda Cleophas, Nganga Joseph Kangethe, Hassanali Ahmed, Diallo Mouhamadou, Kimani Francis T

机构信息

JKUAT Biochemistry Department, Pan African University Institute of Basic Sciences and Technology Innovation, P.O. Box 62000-00200, Nairobi, Kenya.

Department of Medical Laboratory Sciences, College of Health Sciences, Jomo Kenyatta University of Agriculture and Technology, P.O. Box 62000-00200, Nairobi, Kenya.

出版信息

J Parasit Dis. 2023 Mar;47(1):46-58. doi: 10.1007/s12639-022-01537-8. Epub 2022 Oct 13.

Abstract

The emergence and spread of drug resistance of the malaria parasite to the main treatment emphasize the need to develop new antimalarial drugs. In this context, the fatty acid biosynthesis (FAS_II) pathway of the malaria parasite is one of the ideal targets due to its crucial role in parasite survival. In this study, we report the expression and the affinity binding of Fab_I and Fab_Z after exposure to the parasite with different extracts of the . The parasites were exposed for 2 days to different extracts. Gene expression was done to determine the level of expression of the fab enzymes after treatments. A GCMS was run to determine the different compounds of the plant extracts, followed by a virtual screening between the fab enzymes and the active compounds using Pyrex. The results showed different expression patterns of the Fab enzymes. Fab_I expression was downregulated in the W2 and D6 strains by the ethanolic extract but was increased by Hexane and DCM extracts. A different expression pattern was observed for Fab_Z. It was all upregulated except in the D6 strain when exposed to the ethanolic and hexane extracts. Virtual screening showed an affinity with many compounds. Hits compounds with high binding energy were detected. 11alphaHydroxyprogesterone and Aspidospermidin-17-ol were found to have high binding energy with Fab_I respectively (- 10.7 kcal/mol; - 10.2 kcal/mol). Fab_Z shows also high affinity with 11alpha-Hydroxyprogesterone (- 10 kcal/mol) and Thiourea (- 8.4 kcal/mol). This study shows the potential of to be used as a new source of novel antimalarial compounds.

摘要

疟原虫对主要治疗药物的耐药性出现和传播凸显了开发新型抗疟药物的必要性。在此背景下,疟原虫的脂肪酸生物合成(FAS_II)途径因其在寄生虫存活中的关键作用而成为理想靶点之一。在本研究中,我们报告了用[未提及植物名称]的不同提取物处理疟原虫后Fab_I和Fab_Z的表达及亲和结合情况。将疟原虫暴露于不同提取物中2天。进行基因表达检测以确定处理后fab酶的表达水平。运行气相色谱 - 质谱联用仪(GCMS)来确定植物提取物的不同化合物,随后使用Pyrex在fab酶与活性化合物之间进行虚拟筛选。结果显示Fab酶有不同的表达模式。乙醇提取物使W2和D6菌株中的Fab_I表达下调,但己烷和二氯甲烷提取物使其表达增加。Fab_Z观察到不同的表达模式。当暴露于乙醇和己烷提取物时,除D6菌株外它均上调。虚拟筛选显示与许多化合物有亲和力。检测到具有高结合能的命中化合物。发现11α - 羟基孕酮和阿马碱 - 17 - 醇分别与Fab_I具有高结合能(-10.7千卡/摩尔;-10.2千卡/摩尔)。Fab_Z也显示出与11α - 羟基孕酮(-10千卡/摩尔)和硫脲(-8.4千卡/摩尔)有高亲和力。本研究表明[未提及植物名称]有潜力作为新型抗疟化合物的新来源。

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