Molecular Biology and Immunology Department, Fundación Instituto de Inmunología de Colombia (FIDIC), Carrera 50 No. 26-20, Bogotá, Colombia; PhD Programme in Biomedical and Biological Sciences, Universidad del Rosario, Carrera 24 No. 63C-69, Bogotá, Colombia.
Unidad de Proteómica, Instituto de Biología Molecular y Celular del Cáncer -USAL-CSIC, ProteoRed ISCIII, Campus Unamuno, E-37007 Salamanca, Spain.
J Proteomics. 2017 Jan 30;152:131-137. doi: 10.1016/j.jprot.2016.10.018. Epub 2016 Oct 29.
The Aotus nancymaae species has been of great importance in researching the biology and pathogenesis of malaria, particularly for studying Plasmodium molecules for including them in effective vaccines against such microorganism. In spite of the forgoing, there has been no report to date describing the biology of parasite target cells in primates or their biomedical importance. This study was thus designed to analyse A. nancymaae erythrocyte protein composition using MS data collected during a previous study aimed at characterising the Plasmodium vivax proteome and published in the pertinent literature. Most peptides identified were similar to those belonging to 1189 Homo sapiens molecules; >95% of them had orthologues in New World primates. GO terms revealed a correlation between categories having the greatest amount of proteins and vital cell function. Integral membrane molecules were also identified which could be possible receptors facilitating interaction with Plasmodium species. The A. nancymaae erythrocyte proteome is described here for the first time, as a starting point for more in-depth/extensive studies. The data reported represents a source of invaluable information for laboratories interested in carrying out basic and applied biomedical investigation studies which involve using this primate.
An understanding of the proteomics characteristics of A. nancymaae erythrocytes represents a fascinating area for research regarding the study of the pathogenesis of malaria since these are the main target for Plasmodium invasion. However, and even though Aotus is one of the non-human primate models considered most appropriate for biomedical research, knowledge of its proteome, particularly its erythrocytes, remains unknown. According to the above and bearing in mind the lack of information about the A. nancymaae species genome and transcriptome, this study involved a search for primate proteins for comparing their MS/MS spectra with the available information for Homo sapiens. The great similarity found between the primate's molecules and those for humans supported the use of the monkeys or their cells for continuing assays involved in studying malaria. Integral membrane receptors used by Plasmodium for invading cells were also found; this required timely characterisation for evaluating their therapeutic role. The list of erythrocyte protein composition reported here represents a useful source of basic knowledge for advancing biomedical investigation in this field.
奥氏长尾猴(Aotus nancymaae)在研究疟疾的生物学和发病机制方面具有重要意义,特别是在研究疟原虫分子以将其纳入针对此类微生物的有效疫苗方面。尽管如此,迄今为止尚无关于灵长类动物寄生虫靶细胞生物学及其生物医学重要性的报道。因此,本研究旨在使用之前旨在描述间日疟原虫蛋白质组学并在相关文献中发表的研究中收集的 MS 数据来分析奥氏长尾猴红细胞蛋白质组成。鉴定出的大多数肽与属于 1189 个智人物种的肽相似;它们中有>95%的与新世界灵长类动物具有同源物。GO 术语揭示了与具有最大数量蛋白质的类别相关的类别与生命细胞功能之间的相关性。还鉴定了整合膜分子,它们可能是促进与疟原虫属相互作用的可能受体。首次在这里描述了奥氏长尾猴红细胞蛋白质组,作为更深入/广泛研究的起点。报告的数据为有兴趣开展涉及使用这种灵长类动物的基础和应用生物医学研究的实验室提供了宝贵的信息来源。
了解奥氏长尾猴红细胞的蛋白质组学特征是疟疾发病机制研究的一个迷人领域,因为这些是疟原虫入侵的主要靶标。然而,尽管奥氏长尾猴是被认为最适合生物医学研究的非人类灵长类动物模型之一,但对其蛋白质组,特别是其红细胞的了解仍然未知。根据上述情况,并考虑到缺乏有关奥氏长尾猴物种基因组和转录组的信息,本研究涉及寻找灵长类动物蛋白,以便将其 MS/MS 图谱与可用于智人物种的信息进行比较。在灵长类动物的分子与人类的分子之间发现的高度相似性支持使用猴子或其细胞继续进行研究疟疾的实验。还发现了疟原虫用于入侵细胞的整合膜受体;这需要及时进行特征描述,以评估其治疗作用。这里报道的红细胞蛋白组成列表代表了推进该领域生物医学研究的基础知识的有用来源。