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Ionic liquid-based method for direct proteome characterization of velvet antler cartilage

机译:基于离子液体的鹿茸软骨直接蛋白质组学表征方法

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The cartilage zone of the velvet antler is richly vascularized, this being a major difference to the classical cartilage, in which there are no blood vessels. Angiogenesis and rapid growth of vasculature in velvet antler cartilage (VAC) make it an ideal model for discovering the novel angiogenic regulatory factors. However, the proteomic analysis of VAC is challenging due to the serious interference of proteoglycans (PGs) and collagens. To achieve a comprehensive proteome characterization of VAC, herein, we developed an ionic liquid-based method using 1-dodecyl-3-methylimidazolium chloride ([C12-mim]Cl) for selective extraction of cellular proteins from VAC. Compared with the previous cetylpyridinium chloride (CPC)-based method, the developed [C12-mim]Cl-based method takes much less processing time, shows facile preparation procedure and good compatibility towards downstream proteomic analysis, leading to the identification of more protein groups (1543 vs 753), membrane proteins (663 vs 279) and trans membrane proteins (217 vs 58). (C) 2004 Published by Elsevier B.V.
机译:鹿茸的软骨区域血管丰富,这与传统的没有血管的软骨的主要区别。鹿茸软骨(VAC)中血管系统的血管生成和快速生长使其成为发现新型血管生成调节因子的理想模型。但是,由于蛋白聚糖(PGs)和胶原蛋白的严重干扰,VAC的蛋白质组学分析具有挑战性。为了实现VAC的全面蛋白质组表征,我们在本文中开发了一种基于离子液体的方法,使用1-十二烷基-3-甲基咪唑鎓氯化物([C12-mim] Cl)从VAC中选择性提取细胞蛋白。与以前的基于十六烷基氯化吡啶鎓(CPC)的方法相比,已开发的基于[C12-mim] Cl的方法所需的处理时间短得多,显示了简便的制备过程,并与下游蛋白质组学分析具有良好的兼容性,从而可以鉴定更多的蛋白质组(1543 vs 753),膜蛋白(663 vs 279)和跨膜蛋白(217 vs 58)。 (C)2004由Elsevier B.V.发布

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