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-苯基邻氨基苯甲酸衍生物对独脚金内酯受体的抑制作用:结构与功能的深入研究。

Inhibition of strigolactone receptors by -phenylanthranilic acid derivatives: Structural and functional insights.

机构信息

From the New Zealand Institute for Plant and Food Research Limited, Private Bag 92169, Auckland 1142, New Zealand,

From the New Zealand Institute for Plant and Food Research Limited, Private Bag 92169, Auckland 1142, New Zealand.

出版信息

J Biol Chem. 2018 Apr 27;293(17):6530-6543. doi: 10.1074/jbc.RA117.001154. Epub 2018 Mar 9.

Abstract

The strigolactone (SL) family of plant hormones regulates a broad range of physiological processes affecting plant growth and development and also plays essential roles in controlling interactions with parasitic weeds and symbiotic fungi. Recent progress elucidating details of SL biosynthesis, signaling, and transport offers many opportunities for discovering new plant-growth regulators via chemical interference. Here, using high-throughput screening and downstream biochemical assays, we identified -phenylanthranilic acid derivatives as potent inhibitors of the SL receptors from petunia (DAD2), rice (OsD14), and (AtD14). Crystal structures of DAD2 and OsD14 in complex with inhibitors further provided detailed insights into the inhibition mechanism, and modeling of 19 other plant strigolactone receptors suggested that these compounds are active across a large range of plant species. Altogether, these results provide chemical tools for investigating SL signaling and further define a framework for structure-based approaches to design and validate optimized inhibitors of SL receptors for specific plant targets.

摘要

独脚金内酯(SL)是一类植物激素,调控着广泛的生理过程,影响植物生长和发育,同时在调控与寄生杂草和共生真菌的相互作用方面发挥着重要作用。阐明 SL 生物合成、信号转导和运输的最新进展为通过化学干扰发现新的植物生长调节剂提供了许多机会。在这里,我们使用高通量筛选和下游生化分析,鉴定出 - 苯丙氨酸衍生物是矮牵牛(DAD2)、水稻(OsD14)和 (AtD14)SL 受体的有效抑制剂。与抑制剂结合的 DAD2 和 OsD14 的晶体结构进一步提供了对抑制机制的详细了解,并且对其他 19 种植物独脚金内酯受体的建模表明,这些化合物在很大范围内对植物物种具有活性。总之,这些结果为研究 SL 信号转导提供了化学工具,并进一步定义了基于结构的方法的框架,以设计和验证针对特定植物靶标的 SL 受体的优化抑制剂。

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