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用于全蛋白质组鉴定 C16-神经酰胺结合蛋白的叠氮化物标记神经鞘脂。

Azide-tagged sphingolipids for the proteome-wide identification of C16-ceramide-binding proteins.

机构信息

Department of Chemical Biology, Max-Planck-Institute of molecular Physiology, Otto-Hahn-Strasse 11, D-44227 Dortmund, Germany.

出版信息

Chem Commun (Camb). 2018 Dec 4;54(97):13742-13745. doi: 10.1039/c8cc05691a.

Abstract

Ceramide plays key roles in autophagy, inflammation and apoptosis. However, little is known about the molecular mechanisms regulating its function and only a handful of cellular effectors are known for this lipid. Here we show that azide-tagged sphingolipids are powerful tools to identify ceramide targets. The combination of a protein array analysis and a mass spectrometry-based proteomic profiling successfully detects known ceramide-binding proteins and identifies others not yet reported, several of which we validated using a variety of techniques.

摘要

神经酰胺在自噬、炎症和细胞凋亡中起着关键作用。然而,目前对于调节其功能的分子机制知之甚少,而且这种脂质的细胞效应物也只有少数几种。在这里,我们展示了叠氮化物标记的神经酰胺是识别神经酰胺靶标的有力工具。蛋白质芯片分析与基于质谱的蛋白质组学分析相结合,成功地检测到了已知的神经酰胺结合蛋白,并鉴定出了其他尚未报道的蛋白,其中有几种我们使用多种技术进行了验证。

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