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A Chemosensory GPCR as a Potential Target to Control the Root-Knot Nematode Meloidogyne incognita Parasitism in Plants

机译:化学感觉GPCR作为控制植物根结线虫根结线虫寄生的潜在目标

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Root-knot nematodes (RKN), from the Meloidogyne genus, have a worldwide distribution and cause severe economic damage to many life-sustaining crops. Because of their lack of specificity and danger to the environment, most chemical nematicides have been banned from use. Thus, there is a great need for new and safe compounds to control RKN. Such research involves identifying beforehand the nematode proteins essential to the invasion. Since G protein-coupled receptors GPCRs are the target of a large number of drugs, we have focused our research on the identification of putative nematode GPCRs such as those capable of controlling the movement of the parasite towards (or within) its host. A datamining procedure applied to the genome of Meloidogyne incognita allowed us to identify a GPCR, belonging to the neuropeptide GPCR family that can serve as a target to carry out a virtual screening campaign. We reconstructed a 3D model of this receptor by homology modeling and validated it through extensive molecular dynamics simulations. This model was used for large scale molecular dockings which produced a filtered limited set of putative antagonists for this GPCR. Preliminary experiments using these selected molecules allowed the identification of an active compound, namely C260-2124, from the ChemDiv provider, which can serve as a starting point for further investigations.
机译:根结线虫属的根结线虫(RKN)在世界范围内分布,对许多维持生命的农作物造成严重的经济损失。由于缺乏特异性和对环境的危害,大多数化学杀线虫剂已被禁止使用。因此,非常需要新的和安全的化合物来控制RKN。此类研究涉及事先确定入侵所需的线虫蛋白。由于G蛋白偶联受体GPCR是众多药物的目标,因此我们将研究重点放在了鉴定的线虫GPCR的鉴定上,例如能够控制寄生虫向其宿主(或体内)移动的那些。应用于根结线虫的基因组的数据挖掘程序使我们能够鉴定GPCR,该GPCR属于神经肽GPCR家族,可以作为进行虚拟筛选活动的靶标。我们通过同源性建模重建了该受体的3D模型,并通过广泛的分子动力学模拟对其进行了验证。该模型用于大规模分子对接,该对接产生了针对该GPCR的一组有限的假定拮抗剂。使用这些选定分子进行的初步实验使得可以从ChemDiv提供程序中鉴定一种活性化合物,即C260-2124,该化合物可以用作进一步研究的起点。

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