首页> 外文期刊>Journal of molecular recognition: JMR >Structural analysis of the unique insecticidal activity of novel mungbean defensin VrD1 reveals possibility of homoplasy evolution between plant defensins and scorpion neurotoxins.
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Structural analysis of the unique insecticidal activity of novel mungbean defensin VrD1 reveals possibility of homoplasy evolution between plant defensins and scorpion neurotoxins.

机译:对新型绿豆防御素VrD1的独特杀虫活性进行结构分析,揭示了植物防御素与蝎神经毒素之间发生同质进化的可能性。

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摘要

A variety of evolutionarily related defensin molecules is found in plants and animals. Plant gamma-thionins and scorpion neurotoxins, for instance, may be categorized in this functional group, although each class recognizes a distinct receptor binding site. Such molecules are also categorized into the superfamily of cysteine-rich proteins. Plant defensins were generally believed to be involved in antimicrobial or antifungal mechanisms and, unlike scorpion toxins, little is known about whether these molecules are also endowed with the function of insect resistance. We have previously reported the isolation of a cDNA encoding a small cysteine-rich protein designated VrD1 (VrCRP) from a bruchid-resistant mungbean, which is apparently the first discovered plant defensin exhibiting in vitro and in vivo both insecticidal and antifungal activities. Our previous data also successfully demonstrated that VrD1 is toxic to E. coli and able to completely arrest the growth of Sf-21 insect cells at low concentration.However, the molecular and structural basis of this unique insecticidal activity of VrD1 is not clear. Therefore, in the present study, we use structural approach and phylogenic analysis to investigate the evolutionary and functional relations for such unique insecticidal activity. From our results, it is suggested that VrD1, in addition to gamma-thionins and several amylase inhibitors, is highly homologous to scorpion toxins, especially the short toxins. Moreover, based on the observation from our homology structures, VrD1 may utilize a newly found cluster of basic residues to achieve its insecticidal function, whereas all the other plant gamma-thionins were known to use a previously identified basic cluster conserved for gamma-thionins. Considering the general feature of short scorpion toxins to act on insect cell membranes with K(+)- or Cl(-)-channels as molecular targets, our analysis of interaction and recognition modes provides reasonable correlations between this newly found basic cluster and the insecticidal activity of VrD1, which is also comprehended as a possible link for "homoplasy evolution" between plant and animal defensin molecules.
机译:在植物和动物中发现了多种与进化相关的防御素分子。例如,尽管每个类别都可以识别不同的受体结合位点,但植物γ-硫蛋白和蝎子神经毒素可以归为该功能组。此类分子也归类为富含半胱氨酸的蛋白质的超家族。通常认为植物防御素参与抗微生物或抗真菌机制,并且与蝎毒素不同,对于这些分子是否也具有昆虫抗性的功能知之甚少。我们以前曾报道过,从耐布鲁氏菌的绿豆中分离出一种编码小的富含半胱氨酸的小蛋白,称为VrD1(VrCRP)的cDNA,这显然是最早发现的植物防御素,在体外和体内均具有杀虫和抗真菌活性。我们以前的数据也成功地证明了VrD1对大肠杆菌具有毒性,并且能够在低浓度下完全阻止Sf-21昆虫细胞的生长,但是,尚不清楚VrD1这种独特的杀虫活性的分子和结构基础。因此,在本研究中,我们使用结构方法和系统发育分析来研究这种独特的杀虫活性的进化和功能关系。根据我们的研究结果,表明VrD1除了γ-硫ionins和几种淀粉酶抑制剂外,还与蝎毒素(尤其是短毒素)高度同源。此外,基于对我们同源结构的观察,VrD1可能利用新发现的碱性残基簇来实现其杀虫功能,而已知所有其他植物γ-硫蛋白都使用了先前确定的γ-硫蛋白保守的碱性簇。考虑到短蝎毒素通常以K(+)-或Cl(-)-通道为分子靶标作用在昆虫细胞膜上的一般特征,我们的相互作用和识别方式分析提供了这种新发现的基本簇与杀虫剂之间的合理关联VrD1的活性,也被理解为动植物防御素分子之间“同源进化”的可能联系。

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