asiaticcandidatus liberibacterium TcyA潜在抑制剂分子的鉴定与评价

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sapna Lonare , Monica Sharma , Vikram Dalal , Mrugendra Gubyad , Pranav Kumar , Deena Nath Gupta , Akshay Pareek , Shailly Tomar , Dilip Kumar Ghosh , Pravindra Kumar , Ashwani Kumar Sharma
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引用次数: 0

摘要

在Candidatus Liberibacter asiaticus(CLas)ABC转运蛋白家族的两个公认的氨基酸结合周质受体中,胱氨酸结合受体(CLasTcyA)已被证明主要在柑橘植物的韧皮部中表达,是抑制剂开发的靶点。CLasTcyA在与底物的配合物中的晶体结构早已报道。本工作报道了对CLasTcyA抑制潜力的潜在候选物的鉴定和评估。在通过虚拟筛选和MD模拟选择的许多化合物中,吡莫唑、clidinium、柳氮磺胺吡啶和叶酸在与CLasTcyA的复合物中显示出显著更高的亲和力和稳定性。CLasTcyA的SPR研究显示,与胱氨酸(Kd,1.26µM)相比,对吡莫唑和clidinium的结合亲和力显著更高(分别为Kd,2.73 nM和70 nM)与胱氨酸相比。CLasTcyA具有相对较大的结合口袋,其中体积较大的抑制剂非常适合。为评估抑制剂对HLB感染的Mosambi植物的影响而进行的植物内研究表明,与对照植物相比,用抑制剂处理的植物中CLas滴度显著降低。结果表明,在降低处理植物中CLas滴度方面,吡莫齐德比clidinium表现出更高的效率。我们的研究结果表明,针对CLasTcyA等关键蛋白的抑制剂开发可能是HLB管理的重要策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identification and evaluation of potential inhibitor molecules against TcyA from Candidatus Liberibacter asiaticus

Identification and evaluation of potential inhibitor molecules against TcyA from Candidatus Liberibacter asiaticus

Of the two putative amino acid binding periplasmic receptors of ABC transporter family in Candidatus Liberibacter asiaticus (CLas), cystine binding receptor (CLasTcyA) has been shown to mainly express in phloem of citrus plant and is a target for inhibitor development. The crystal structure of CLasTcyA in complex with substrates has been reported earlier. The present work reports the identification and evaluation of potential candidates for their inhibitory potential against CLasTcyA. Among many compounds, selected through virtual screening, and MD simulation, pimozide, clidinium, sulfasalazine and folic acid showed significantly higher affinities and stability in complex with CLasTcyA. The SPR studies with CLasTcyA revealed significantly higher binding affinities for pimozide and clidinium (Kd, 2.73 nM and 70 nM, respectively) as compared to cystine (Kd, 1.26 µM). The higher binding affinities could be attributed to significantly increased number of interactions in the binding pocket as evident from the crystal structures of CLasTcyA in complex with pimozide and clidinium as compared to cystine. The CLasTcyA possess relatively large binding pocket where bulkier inhibitors fit quite well. In planta studies, carried out to assess the effect of inhibitors on HLB infected Mosambi plants, showed significant reduction in CLas titre in plants treated with inhibitors as compared to control plants. The results showed that pimozide exhibited higher efficiency as compared to clidinium in reducing CLas titre in treated plants. Our results showed that the inhibitor development against critical proteins like CLasTcyA can be an important strategy in management of HLB.

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来源期刊
Journal of structural biology
Journal of structural biology 生物-生化与分子生物学
CiteScore
6.30
自引率
3.30%
发文量
88
审稿时长
65 days
期刊介绍: Journal of Structural Biology (JSB) has an open access mirror journal, the Journal of Structural Biology: X (JSBX), sharing the same aims and scope, editorial team, submission system and rigorous peer review. Since both journals share the same editorial system, you may submit your manuscript via either journal homepage. You will be prompted during submission (and revision) to choose in which to publish your article. The editors and reviewers are not aware of the choice you made until the article has been published online. JSB and JSBX publish papers dealing with the structural analysis of living material at every level of organization by all methods that lead to an understanding of biological function in terms of molecular and supermolecular structure. Techniques covered include: • Light microscopy including confocal microscopy • All types of electron microscopy • X-ray diffraction • Nuclear magnetic resonance • Scanning force microscopy, scanning probe microscopy, and tunneling microscopy • Digital image processing • Computational insights into structure
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