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膜糖组学揭示了细胞表面唾液酸化的异质性和定量分布。

Membrane glycomics reveal heterogeneity and quantitative distribution of cell surface sialylation.

作者信息

Park Diane Dayoung, Xu Gege, Wong Maurice, Phoomak Chatchai, Liu Mingqi, Haigh Nathan E, Wongkham Sopit, Yang Pengyuan, Maverakis Emanual, Lebrilla Carlito B

机构信息

Department of Chemistry , University of California , Davis , CA 95616 , USA.

Department of Surgery , Beth Israel Deaconess Medical Center , Harvard Medical School , Boston , MA 02115 , USA . Email:

出版信息

Chem Sci. 2018 Jun 27;9(29):6271-6285. doi: 10.1039/c8sc01875h. eCollection 2018 Aug 7.

Abstract

Given that unnatural sugar expression is metabolically achieved, the kinetics and disposition of incorporation can lend insight into the temporal and localization preferences of sialylation across the cell surface. However, common detection schemes lack the ability to detail the molecular diversity and distribution of target moieties. Here we employed a mass spectrometric approach to trace the placement of azido sialic acids on membrane glycoconjugates, which revealed substantial variations in incorporation efficiencies between -/-glycans, glycosites, and glycosphingolipids. To further explore the propensity for sialylation, we subsequently mapped the native glycome of model epithelial cell surfaces and illustrate that while glycosylation sites span broadly across the extracellular region, a higher number of heterogeneous glycoforms occur on sialylated sites closest to the transmembrane domain. Beyond imaging techniques, this integrative approach provides unprecedented details about the frequency and structure-specific distribution of cell surface sialylation, a critical feature that regulates cellular interactions and homeostatic pathways.

摘要

鉴于非天然糖的表达是通过代谢实现的,糖基化的动力学和掺入情况可以深入了解整个细胞表面唾液酸化的时间和定位偏好。然而,常见的检测方法缺乏详细描述靶标部分分子多样性和分布的能力。在这里,我们采用质谱方法追踪叠氮唾液酸在膜糖缀合物上的位置,结果显示在不同的聚糖、糖基化位点和糖鞘脂之间,掺入效率存在显著差异。为了进一步探究唾液酸化的倾向,我们随后绘制了模型上皮细胞表面的天然糖组图谱,并表明虽然糖基化位点广泛分布于细胞外区域,但在最靠近跨膜结构域的唾液酸化位点上出现了更多种类的糖型。除了成像技术外,这种综合方法提供了关于细胞表面唾液酸化的频率和结构特异性分布的前所未有的详细信息,这是调节细胞相互作用和稳态途径的关键特征。

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