首页> 外文期刊>Pesticide Biochemistry and Physiology >Re-invigorating the insecticide discovery pipeline for vector control: GPCRs as targets for the identification of next gen insecticides. (Special Issue: Advances in vector and urban pest management and resistance.)
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Re-invigorating the insecticide discovery pipeline for vector control: GPCRs as targets for the identification of next gen insecticides. (Special Issue: Advances in vector and urban pest management and resistance.)

机译:重新激发用于载体控制的杀虫剂发现流程:将GPCR作为鉴定下一代杀虫剂的目标。 (特刊:病媒和城市病虫害管理和抗性的进展。)

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摘要

G protein-coupled receptors (GPCRs) comprise a large family of membrane-bound molecules that mediate critical physiological roles in both vertebrates and invertebrates. GPCRs are widely exploited targets of the pharmaceutical industry; approximately 50% of human drugs interact with these receptors. GPCRs are also candidate targets for next-generation insecticides and provide opportunities to discover new mode-of-action chemistries for insect control. We present an overview of the Purdue Insecticide Discovery Pipeline which employs a target-based "genome-to-lead" approach to identify novel insecticidal molecules. The pipeline is focused on invertebrate GPCRs, with an emphasis on mosquito and tick dopamine receptors (DARs). We summarize published studies describing the characteristics of D1-like (G alpha s coupled) DARs from the yellow fever mosquito, Aedes aegypti (AaDOP1, AaDOP2) and Lyme disease tick, Ixodes scapularis (IsDOP1, IsDOP2), and review our ongoing cell-based chemical library screening efforts to discover small molecule ligands and modulators of AaDOP2 and IsDOP2. We discuss "hit-to-lead" optimization of AaDOP2 antagonists and present in vivo assay data demonstrating that lead antagonists cause rapid and high mortality of Ae. aegypti larvae. To expand capabilities of the pipeline, we developed an in vitro screen to identify small molecule agonists of AaDOP2. Twenty-five agonists were discovered in the screen that exhibited significant potency at AaDOP2, although a subset of the hits that were tested (SKF82958, SKF81297) showed no evidence of in vivo toxicity to Ae. aegypti larvae. Finally, we analyze the conceptual protein sequence of D1-like DARs from the malaria mosquito, Anopheles gambiae and the northern-house mosquito, Culex quinquefasciatus, and discuss the potential application of GPCR target-based insecticide discovery for other mosquito vectors of importance to human health.
机译:G蛋白偶联受体(GPCR)包含大家族的膜结合分子,在脊椎动物和无脊椎动物中介导关键的生理作用。 GPCR是制药行业广泛使用的目标。大约50%的人类药物与这些受体相互作用。 GPCR也是下一代杀虫剂的候选目标,并提供了发现新的作用方式化学物质以控制昆虫的机会。我们介绍了普渡杀虫剂发现管道的概述,该管道采用基于目标的“基因组到铅”方法来鉴定新型杀虫分子。该计划的重点是无脊椎动物GPCR,重点是蚊子和壁虱多巴胺受体(DARs)。我们总结了已发表的研究,这些研究描述了黄热蚊,埃及伊蚊(AaDOP1,AaDOP2)和莱姆病tick的D 1 样(G alpha s 偶联)DAR的特征。 ,肩x骨(IsDOP1,IsDOP2),并回顾我们正在进行的基于细胞的化学文库筛选工作,以发现AaDOP2和IsDOP2的小分子配体和调节剂。我们讨论了AaDOP2拮抗剂的“命中至领先”优化,并提出了体内测定数据,证明了领先的拮抗剂引起Ae的快速和高死亡率。埃及伊蚊幼虫。为了扩展管道的功能,我们开发了体外筛选来鉴定AaDOP2的小分子激动剂。在筛选中发现了二十五个激动剂,它们在AaDOP2上显示出显着的效价,尽管测试的部分命中子集(SKF82958,SKF81297)没有显示出对Ae的体内毒性证据。埃及伊蚊幼虫。最后,我们分析了来自疟疾蚊子,冈比亚按蚊和北部蚊子库克斯库蚊的D 1 类DARs的概念蛋白序列,并讨论了基于GPCR目标的杀虫剂发现的潜在应用用于其他对人类健康重要的蚊媒。

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