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全球大鼠和人类血小板蛋白质组分析 - 阐明多功能血小板和跨物种功能进化的分子蓝图。

Global analysis of the rat and human platelet proteome - the molecular blueprint for illustrating multi-functional platelets and cross-species function evolution.

机构信息

Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China.

出版信息

Proteomics. 2010 Jul;10(13):2444-57. doi: 10.1002/pmic.200900271.

DOI:10.1002/pmic.200900271
PMID:20443191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4302335/
Abstract

Emerging evidences indicate that blood platelets function in multiple biological processes including immune response, bone metastasis and liver regeneration in addition to their known roles in hemostasis and thrombosis. Global elucidation of platelet proteome will provide the molecular base of these platelet functions. Here, we set up a high-throughput platform for maximum exploration of the rat/human platelet proteome using integrated proteomic technologies, and then applied to identify the largest number of the proteins expressed in both rat and human platelets. After stringent statistical filtration, a total of 837 unique proteins matched with at least two unique peptides were precisely identified, making it the first comprehensive protein database so far for rat platelets. Meanwhile, quantitative analyses of the thrombin-stimulated platelets offered great insights into the biological functions of platelet proteins and therefore confirmed our global profiling data. A comparative proteomic analysis between rat and human platelets was also conducted, which revealed not only a significant similarity, but also an across-species evolutionary link that the orthologous proteins representing "core proteome", and the "evolutionary proteome" is actually a relatively static proteome.

摘要

新兴证据表明,血小板除了在止血和血栓形成中的已知作用外,还在免疫反应、骨转移和肝脏再生等多种生物过程中发挥作用。对血小板蛋白质组的全面阐明将为这些血小板功能提供分子基础。在这里,我们使用集成的蛋白质组学技术建立了一个高通量平台,以最大限度地探索大鼠/人血小板蛋白质组,然后应用于鉴定大鼠和人血小板中表达的最多数量的蛋白质。经过严格的统计过滤,共鉴定出 837 个独特的蛋白质,每个蛋白质至少匹配两个独特的肽,这使其成为迄今为止大鼠血小板的第一个全面蛋白质数据库。同时,对凝血酶刺激的血小板进行定量分析,深入了解了血小板蛋白质的生物学功能,从而证实了我们的全局分析数据。还对大鼠和人血小板进行了比较蛋白质组学分析,结果不仅显示出高度的相似性,而且还显示出跨物种进化联系,即代表“核心蛋白质组”的同源蛋白质,以及“进化蛋白质组”实际上是一个相对静态的蛋白质组。

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