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班氏丝虫在宿主/寄生虫界面分泌/排泄的蛋白:阶段和性别特异性蛋白质组分析。

Brugia malayi excreted/secreted proteins at the host/parasite interface: stage- and gender-specific proteomic profiling.

机构信息

Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.

出版信息

PLoS Negl Trop Dis. 2009;3(4):e410. doi: 10.1371/journal.pntd.0000410. Epub 2009 Apr 7.

Abstract

Relatively little is known about the filarial proteins that interact with the human host. Although the filarial genome has recently been completed, protein profiles have been limited to only a few recombinants or purified proteins of interest. Here, we describe a large-scale proteomic analysis using microcapillary reverse-phase liquid chromatography-tandem-mass spectrometry to identify the excretory-secretory (ES) products of the L3, L3 to L4 molting ES, adult male, adult female, and microfilarial stages of the filarial parasite Brugia malayi. The analysis of the ES products from adult male, adult female, microfilariae (Mf), L3, and molting L3 larvae identified 852 proteins. Annotation suggests that the functional and component distribution was very similar across each of the stages studied; however, the Mf contributed a higher proportion to the total number of identified proteins than the other stages. Of the 852 proteins identified in the ES, only 229 had previous confirmatory expressed sequence tags (ESTs) in the available databases. Moreover, this analysis was able to confirm the presence of 274 "hypothetical" proteins inferred from gene prediction algorithms applied to the B. malayi (Bm) genome. Not surprisingly, the majority (160/274) of these "hypothetical" proteins were predicted to be secreted by Signal IP and/or SecretomeP 2.0 analysis. Of major interest is the abundance of previously characterized immunomodulatory proteins such as ES-62 (leucyl aminopeptidase), MIF-1, SERPIN, glutathione peroxidase, and galectin in the ES of microfilariae (and Mf-containing adult females) compared to the adult males. In addition, searching the ES protein spectra against the Wolbachia database resulted in the identification of 90 Wolbachia-specific proteins, most of which were metabolic enzymes that have not been shown to be immunogenic. This proteomic analysis extends our knowledge of the ES and provides insight into the host-parasite interaction.

摘要

关于与人体宿主相互作用的丝虫蛋白,人们知之甚少。尽管丝虫基因组最近已经完成,但蛋白质图谱仅限于少数感兴趣的重组蛋白或纯化蛋白。在这里,我们描述了一种使用微毛细管反相液相色谱-串联质谱进行的大规模蛋白质组学分析,以鉴定丝虫寄生虫班氏吴策线虫的 L3、L3 到 L4 蜕皮 ES、成虫雄性、成虫雌性和微丝蚴阶段的排泄-分泌(ES)产物。对成虫雄性、成虫雌性、微丝蚴(Mf)、L3 和蜕皮 L3 幼虫的 ES 产物进行分析,鉴定出 852 种蛋白质。注释表明,在所研究的每个阶段,功能和成分分布都非常相似;然而,Mf 比其他阶段贡献了更高比例的总鉴定蛋白数。在 ES 中鉴定出的 852 种蛋白质中,只有 229 种在现有的数据库中具有先前确认的表达序列标签(EST)。此外,这项分析能够确认从应用于班氏吴策线虫(Bm)基因组的基因预测算法推断出的 274 种“假设”蛋白质的存在。毫不奇怪,这些“假设”蛋白质中的大多数(160/274)被信号 IP 和/或 SecretomeP 2.0 分析预测为分泌蛋白。最引人注目的是,与成年雄性相比,在微丝蚴(和含微丝蚴的成年雌性)的 ES 中,以前表征的免疫调节蛋白如 ES-62(亮氨酰氨基肽酶)、MIF-1、丝氨酸蛋白酶抑制剂、谷胱甘肽过氧化物酶和半乳糖凝集素的丰度很高。此外,将 ES 蛋白图谱与沃尔巴克氏体数据库进行比对,鉴定出 90 种沃尔巴克氏体特异性蛋白,其中大多数是代谢酶,尚未证明具有免疫原性。这项蛋白质组学分析扩展了我们对 ES 的认识,并深入了解了宿主-寄生虫的相互作用。

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