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人类血小板的磷酸化蛋白质组学:探索新的激活途径。

Phosphoproteomics of human platelets: A quest for novel activation pathways.

作者信息

Zahedi René P, Begonja Antonija J, Gambaryan Stepan, Sickmann Albert

机构信息

Protein Mass Spectrometry and Functional Proteomics Group, Rudolf-Virchow-Center for Experimental Biomedicine, University of Wuerzburg, Versbacher Str. 9, 97078 Wuerzburg, Germany.

出版信息

Biochim Biophys Acta. 2006 Dec;1764(12):1963-76. doi: 10.1016/j.bbapap.2006.08.017. Epub 2006 Sep 7.

Abstract

Besides their role in hemostasis, platelets are also highly involved in the pathogenesis and progression of cardiovascular diseases. Since important and initial steps of platelet activation and aggregation are regulated by phosphorylation events, a comprehensive study aimed at the characterization of phosphorylation-driven signaling cascades might lead to the identification of new target proteins for clinical research. However, it becomes increasingly evident that only a comprehensive phosphoproteomic approach may help to characterize functional protein networks and their dynamic alteration during physiological and pathophysiological processes in platelets. In this review, we discuss current methodologies in phosphoproteome research including their potentials as well as limitations, from sample preparation to classical approaches like radiolabeling and state-of-the-art mass spectrometry techniques.

摘要

除了在止血过程中发挥作用外,血小板还高度参与心血管疾病的发病机制和进展。由于血小板激活和聚集的重要初始步骤受磷酸化事件调控,一项旨在表征磷酸化驱动信号级联反应的全面研究可能会促成临床研究中新靶蛋白的鉴定。然而,越来越明显的是,只有全面的磷酸化蛋白质组学方法才可能有助于表征血小板在生理和病理生理过程中的功能蛋白网络及其动态变化。在本综述中,我们讨论了磷酸化蛋白质组研究中的当前方法,包括从样品制备到放射性标记等经典方法以及最新的质谱技术等方法的潜力和局限性。

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