脱落酸
立体专一性
突变
受体
生物化学
位阻效应
立体化学
结合位点
化学
生物
突变体
催化作用
基因
作者
Xingliang Zhang,Lun Jiang,Guoqiang Wang,Lin Yu,Qi Zhang,Xin Qi,Wei Wu,Zhizhong Gong,Zhongzhou Chen
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2013-07-02
卷期号:8 (7): e67477-e67477
被引量:44
标识
DOI:10.1371/journal.pone.0067477
摘要
The phytohormone abscisic acid ((+)-ABA) plays a key role in many processes. The biological and biochemical activities of unnatural (-)-ABA have been extensively investigated since 1960s. However, the recognition mechanism by which only a few members among PYR/PYL/RCAR (PYLs) family can bind (-)-ABA remains largely unknown. Here we systematically characterized the affinity of PYLs binding to the (-)-ABA and reported the crystal structures of apo-PYL5, PYL3-(-)-ABA and PYL9-(+)-ABA. PYL5 showed the strongest binding affinity with (-)-ABA among all the PYLs. PYL9 is a stringently exclusive (+)-ABA receptor with interchangeable disulfide bonds shared by a subclass of PYLs. PYL3 is a dual receptor to both ABA enantiomers. The binding orientation and pocket of (-)-ABA in PYLs are obviously different from those of (+)-ABA. Steric hindrance and hydrophobic interaction are the two key factors in determining the stereospecificity of PYLs binding to (-)-ABA, which is further confirmed by gain-of-function and loss-of-function mutagenesis. Our results provide novel insights of the bioactivity of ABA enantiomers onto PYLs, and shed light on designing the selective ABA receptors agonists.
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