首页> 美国卫生研究院文献>Toxins >Functional Elucidation of Nemopilema nomurai and Cyanea nozakii Nematocyst Venoms’ Lytic Activity Using Mass Spectrometry and Zymography
【2h】

Functional Elucidation of Nemopilema nomurai and Cyanea nozakii Nematocyst Venoms’ Lytic Activity Using Mass Spectrometry and Zymography

机译:质谱和Zymography解析Nemopilema nomurai和Cyanea nozakii Nematocyst毒液的溶解活性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Background: Medusozoans utilize explosively discharging penetrant nematocysts to inject venom into prey. These venoms are composed of highly complex proteins and peptides with extensive bioactivities, as observed in vitro. Diverse enzymatic toxins have been putatively identified in the venom of jellyfish, Nemopilema nomurai and Cyanea nozakii, through examination of their proteomes and transcriptomes. However, functional examination of putative enzymatic components identified in proteomic approaches to elucidate potential bioactivities is critically needed. Methods: In this study, enzymatic toxins were functionally identified using a combined approach consisting of in gel zymography and liquid chromatography tandem mass spectrometry (LC-MS/MS). The potential roles of metalloproteinases and lipases in hemolytic activity were explored using specific inhibitors. Results: Zymography indicated that nematocyst venom possessed protease-, lipase- and hyaluronidase-class activities. Further, proteomic approaches using LC-MS/MS indicated sequence homology of proteolytic bands observed in zymography to extant zinc metalloproteinase-disintegrins and astacin metalloproteinases. Moreover, pre-incubation of the metalloproteinase inhibitor batimastat with N. nomurai nematocyst venom resulted in an approximate 62% reduction of hemolysis compared to venom exposed sheep erythrocytes, suggesting that metalloproteinases contribute to hemolytic activity. Additionally, species within the molecular mass range of 14–18 kDa exhibited both egg yolk and erythrocyte lytic activities in gel overlay assays. Conclusion: For the first time, our findings demonstrate the contribution of jellyfish venom metalloproteinase and suggest the involvement of lipase species to hemolytic activity. Investigations of this relationship will facilitate a better understanding of the constituents and toxicity of jellyfish venom.
机译:背景:中生动物利用爆炸性释放的渗透性线虫囊将毒液注入猎物。如体外观察到的,这些毒液由高度复杂的蛋白质和具有广泛生物活性的肽组成。通过检查它们的蛋白质组和转录组,已在水母,野村线虫(Nemopilema nomurai)和Cyanea nozakii的毒液中推定了多种酶毒素。但是,迫切需要在蛋白质组学方法中鉴定出的假定酶成分进行功能检查,以阐明潜在的生物活性。方法:在这项研究中,使用凝胶酶色谱法和液相色谱串联质谱法(LC-MS / MS)组成的组合方法在功能上鉴定了酶毒素。使用特定的抑制剂探索了金属蛋白酶和脂肪酶在溶血活性中的潜在作用。结果:线描法表明线虫囊毒液具有蛋白酶,脂肪酶和透明质酸酶类的活性。此外,使用LC-MS / MS的蛋白质组学方法表明,在酶谱学中观察到的蛋白水解条带与现有的锌金属蛋白酶-双整合素和阿斯塔霉素金属蛋白酶的序列同源性。此外,与暴露有毒液的绵羊红细胞相比,金属蛋白酶抑制剂batimastat与野村奈瑟氏球囊毒液的预孵育导致溶血作用降低约62%,这表明金属蛋白酶有助于溶血活性。此外,分子量在14–18 kDa范围内的物种在凝胶覆盖试验中显示出蛋黄和红细胞溶解活性。结论:我们的发现首次证明了水母毒液金属蛋白酶的贡献,并暗示了脂肪酶种类与溶血活性的关系。对这种关系的研究将有助于更好地了解水母毒液的成分和毒性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号