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靶向人类细胞和斑马鱼中声波刺猬蛋白胆固醇化修饰的新型化学探针

New chemical probes targeting cholesterylation of Sonic Hedgehog in human cells and zebrafish.

作者信息

Ciepla Paulina, Konitsiotis Antonios D, Serwa Remigiusz A, Masumoto Naoko, Leong Wai P, Dallman Margaret J, Magee Anthony I, Tate Edward W

机构信息

Department of Chemistry , Imperial College London , Exhibition Road , London SW7 2AZ , UK . Email:

National Heart and Lung Institute , Imperial College London , Exhibition Road , London SW7 2AZ , UK.

出版信息

Chem Sci. 2014 May 1;5(11):4249-4259. doi: 10.1039/c4sc01600a. Epub 2014 Aug 15.

Abstract

Sonic Hedgehog protein (Shh) is a morphogen molecule important in embryonic development and in the progression of many cancer types in which it is aberrantly overexpressed. Fully mature Shh requires attachment of cholesterol and palmitic acid to its C- and N-termini, respectively. The study of lipidated Shh has been challenging due to the limited array of tools available, and the roles of these posttranslational modifications are poorly understood. Herein, we describe the development and validation of optimised alkynyl sterol probes that efficiently tag Shh cholesterylation and enable its visualisation and analysis through bioorthogonal ligation to reporters. An optimised probe was shown to be an excellent cholesterol biomimetic in the context of Shh, enabling appropriate release of tagged Shh from signalling cells, formation of multimeric transport complexes and signalling. We have used this probe to determine the size of transport complexes of lipidated Shh in culture medium and expression levels of endogenous lipidated Shh in pancreatic ductal adenocarcinoma cell lines through quantitative chemical proteomics, as well as direct visualisation of the probe by fluorescence microscopy and detection of cholesterylated Hedgehog protein in developing zebrafish embryos. These sterol probes provide a set of novel and well-validated tools that can be used to investigate the role of lipidation on activity of Shh, and potentially other members of the Hedgehog protein family.

摘要

音猬因子蛋白(Shh)是一种形态发生素分子,在胚胎发育以及许多异常过度表达的癌症类型进展中具有重要作用。完全成熟的Shh分别需要在其C端和N端连接胆固醇和棕榈酸。由于可用工具有限,对脂质化Shh的研究一直具有挑战性,并且这些翻译后修饰的作用尚不清楚。在此,我们描述了优化的炔基甾醇探针的开发和验证,该探针可有效标记Shh的胆固醇化,并通过与报告分子的生物正交连接实现其可视化和分析。在Shh的背景下,优化后的探针被证明是一种出色的胆固醇模拟物,能够使标记的Shh从信号细胞中适当释放,形成多聚体转运复合物并进行信号传导。我们已使用该探针通过定量化学蛋白质组学来确定培养基中脂质化Shh转运复合物的大小以及胰腺导管腺癌细胞系中内源性脂质化Shh的表达水平,同时通过荧光显微镜直接观察探针并检测斑马鱼胚胎发育过程中胆固醇化的刺猬蛋白。这些甾醇探针提供了一套经过充分验证的新型工具,可用于研究脂质化对Shh活性以及刺猬蛋白家族其他潜在成员的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98e7/4285107/b2fe87725844/c4sc01600a-f1.jpg

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