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首页> 外文期刊>Insect Molecular Biology >Insights into the venom composition of the ectoparasitoid wasp Nasonia vitripennis from bioinformatic and proteomic studies. (Special Issue: The Nasonia genome.)
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Insights into the venom composition of the ectoparasitoid wasp Nasonia vitripennis from bioinformatic and proteomic studies. (Special Issue: The Nasonia genome.)

机译:通过生物信息学和蛋白质组学研究,了解类外寄生物黄蜂 vitripennis 的毒液成分。 (特刊:Nasonia基因组。)

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摘要

With the Nasonia vitripennis genome sequences available, we attempted to determine the proteins present in venom by two different approaches. First, we searched for the transcripts of venom proteins by a bioinformatic approach using amino acid sequences of known hymenopteran venom proteins. Second, we performed proteomic analyses of crude N. vitripennis venom removed from the venom reservoir, implementing both an off-line two-dimensional liquid chromatography matrix-assisted laser desorption/ionization time-of-flight (2D-LC-MALDI-TOF) mass spectrometry (MS) and a two-dimensional liquid chromatography electrospray ionization Founer transform ion cyclotron resonance (2D-LC-ESI-FT-ICR) MS setup. This combination of bioinformatic and proteomic studies resulted in an extraordinary richness of identified venom constituents. Moreover, half of the 79 identified proteins were not yet associated with insect venoms: 16 proteins showed similarity only to known proteins from other tissues or secretions, and an additional 23 did not show similarity to any known protein. Serine proteases and their inhibitors were the most represented. Fifteen nonsecretory proteins were also identified by proteomic means and probably represent so-called 'venom trace elements'. The present study contributes greatly to the understanding of the biological diversity of the venom of parasitoid wasps at the molecular level.
机译:利用可利用的Nasonia vitripennis基因组序列,我们尝试通过两种不同的方法来确定存在于毒液中的蛋白质。首先,我们使用已知的膜翅目蛇毒蛋白的氨基酸序列,通过生物信息学方法搜索蛇毒蛋白的转录本。第二,我们对粗制氮素进行了蛋白质组学分析。从毒液库中取出vitripennis毒液,同时实施离线二维液相色谱基质辅助激光解吸/电离飞行时间(2D-LC-MALDI-TOF)质谱(MS)和二维液相色谱电喷雾电离Founer变换离子回旋共振(2D-LC-ESI-FT-ICR)MS设置。生物信息学和蛋白质组学研究的这种结合导致了确定的毒液成分异常丰富。此外,已鉴定的79种蛋白质中有一半尚未与昆虫毒液结合:16种蛋白质仅与来自其他组织或分泌物的已知蛋白质相似,另外23种与任何已知蛋白质均未相似。丝氨酸蛋白酶及其抑制剂是最典型的。还通过蛋白质组学方法鉴定了15种非分泌蛋白,它们可能代表了所谓的“毒液微量元素”。本研究为在分子水平上对寄生蜂的毒液生物学多样性的理解做出了巨大贡献。

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