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一种化感 GPCR 作为控制植物根结线虫寄生的潜在靶标。

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

机构信息

Université de Lorraine, CNRS, Inria, LORIA, F-54000 Nancy, France.

EMBRAPA Genetic Resources and Biotechnology, Brasilia 70770-917, DF, Brazil.

出版信息

Molecules. 2019 Oct 22;24(20):3798. doi: 10.3390/molecules24203798.

DOI:10.3390/molecules24203798
PMID:31652525
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6832152/
Abstract

Root-knot nematodes (RKN), from the 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 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.

摘要

根结线虫(RKN)属于根结线虫属,分布广泛,对许多维持生命的作物造成严重的经济损失。由于大多数化学杀线虫剂缺乏特异性和对环境的危害,它们已被禁止使用。因此,需要新的安全化合物来控制 RKN。此类研究涉及事先识别对线虫入侵至关重要的蛋白质。由于 G 蛋白偶联受体 (GPCR) 是大量药物的靶点,我们的研究重点是鉴定假定的线虫 GPCR,例如那些能够控制寄生虫向(或在)其宿主移动的 GPCR。应用于基因组的数据挖掘程序允许我们鉴定一种属于神经肽 GPCR 家族的 GPCR,它可以作为靶标来进行虚拟筛选。我们通过同源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,产生了针对该 GPCR 的有限数量的假定拮抗剂。使用这些选定分子进行的初步实验鉴定出一种来自 ChemDiv 供应商的活性化合物 C260-2124,它可以作为进一步研究的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b1857b954896/molecules-24-03798-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b504a998b37f/molecules-24-03798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/a699fb3238f3/molecules-24-03798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/2787b0805016/molecules-24-03798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/0465c6768ec2/molecules-24-03798-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b078d4e4abc7/molecules-24-03798-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b1857b954896/molecules-24-03798-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b504a998b37f/molecules-24-03798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/a699fb3238f3/molecules-24-03798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/2787b0805016/molecules-24-03798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/0465c6768ec2/molecules-24-03798-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b078d4e4abc7/molecules-24-03798-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/6832152/b1857b954896/molecules-24-03798-g008.jpg

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