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Towards further defining the proteome of mouse saliva

机译:进一步定义小鼠唾液的蛋白质组

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Background Knowledge of the mouse salivary proteome is not well documented and as a result, very limited. Currently, several salivary proteins remain unidentified and for some others, their function yet to be determined. The goal of the present study is to utilize mass spectrometry analysis to widen our knowledge of mouse salivary proteins, and through extensive database searches, provide further insight into the array of proteins that can be found in saliva. A comprehensive mouse salivary proteome will also facilitate the development of mouse models to study specific biomarkers of many human diseases. Results Individual saliva samples were collected from male and female mice, and later pooled according to sex. Two pools of saliva from female mice (2 samples/pool) and 2 pools of saliva from male mice were used for analysis utilizing high performance liquid chromatograph mass spectrometry (nano-RPLC-MS/MS). The resulting datasets identified 345 proteins: 174 proteins were represented in saliva obtained from both sexes, as well as 82 others that were more female specific and 89 that were more male specific. Of these sex linked proteins, twelve were identified as exclusively sex-limited; 10 unique to males and 2 unique to females. Functional analysis of the 345 proteins identified 128 proteins with catalytic activity characteristics; indicative of proteins involved in digestion, and 35 proteins associated with stress response, host defense, and wound healing functions. Submission of the list of 345 proteins to the BioMart data mining tool in the Ensembl database further allowed us to identify a total of 283 orthologous human genes, of which, 131 proteins were recently reported to be present in the human salivary proteome. Conclusions The present study is the most comprehensive list to date of the proteins that constitute the mouse salivary proteome. The data presented can serve as a useful resource for identifying potentially useful biomarkers of human health and disease.
机译:背景技术小鼠唾液蛋白质组的知识尚不完善,因此非常有限。目前,几种唾液蛋白尚未鉴定,而对于另一些唾液蛋白,其功能尚待确定。本研究的目的是利用质谱分析来扩展我们对小鼠唾液蛋白的认识,并通过广泛的数据库搜索,提供对唾液中蛋白质序列的进一步了解。全面的小鼠唾液蛋白质组学也将促进小鼠模型的开发,以研究许多人类疾病的特定生物标记。结果从雄性和雌性小鼠中收集了单独的唾液样本,然后根据性别进行了合并。利用高效液相色谱质谱法(nano-RPLC-MS / MS),将雌性小鼠的两个唾液池(2个样品/池)和雄性小鼠的2个唾液池用于分析。结果数据集鉴定出345种蛋白质:从男女获得的唾液中代表174种蛋白质,另外82种女性特异性更高,89种男性特异性更高。在这些与性相关的蛋白质中,有十二种被确定为仅受性别限制。男性独有10个,女性独有2个。 345种蛋白质的功能分析确定了128种具有催化活性特征的蛋白质。表示参与消化的蛋白质,以及35种与应激反应,宿主防御和伤口愈合功能有关的蛋白质。向Ensembl数据库中的BioMart数据挖掘工具提交了345种蛋白质的列表,这进一步使我们能够鉴定出总共283个直系同源人类基因,其中最近有131种蛋白质据报道存在于人类唾液蛋白质组中。结论本研究是迄今为止构成小鼠唾液蛋白质组的蛋白质的最全面清单。所提供的数据可以用作识别人类健康和疾病的潜在有用生物标志物的有用资源。

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