首页> 美国卫生研究院文献>Molecular Cellular Proteomics : MCP >Human Plasma N-glycosylation as Analyzed by Matrix-Assisted Laser Desorption/Ionization-Fourier Transform Ion Cyclotron Resonance-MS Associates with Markers of Inflammation and Metabolic Health
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Human Plasma N-glycosylation as Analyzed by Matrix-Assisted Laser Desorption/Ionization-Fourier Transform Ion Cyclotron Resonance-MS Associates with Markers of Inflammation and Metabolic Health

机译:基质辅助激光解吸/电离-傅立叶变换离子回旋共振-MS与炎症和代谢健康标志物关联分析人体血浆N-糖基化

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摘要

Glycosylation is an abundant co- and post-translational protein modification of importance to protein processing and activity. Although not template-defined, glycosylation does reflect the biological state of an organism and is a high-potential biomarker for disease and patient stratification. However, to interpret a complex but informative sample like the total plasma N-glycome, it is important to establish its baseline association with plasma protein levels and systemic processes. Thus far, large-scale studies (n >200) of the total plasma N-glycome have been performed with methods of chromatographic and electrophoretic separation, which, although being informative, are limited in resolving the structural complexity of plasma N-glycans. MS has the opportunity to contribute additional information on, among others, antennarity, sialylation, and the identity of high-mannose type species.Here, we have used matrix-assisted laser desorption/ionization (MALDI)-Fourier transform ion cyclotron resonance (FTICR)-MS to study the total plasma N-glycome of 2144 healthy middle-aged individuals from the Leiden Longevity Study, to allow association analysis with markers of metabolic health and inflammation. To achieve this, N-glycans were enzymatically released from their protein backbones, labeled at the reducing end with 2-aminobenzoic acid, and following purification analyzed by negative ion mode intermediate pressure MALDI-FTICR-MS. In doing so, we achieved the relative quantification of 61 glycan compositions, ranging from Hex4HexNAc2 to Hex7HexNAc6dHex1Neu5Ac4, as well as that of 39 glycosylation traits derived thereof. Next to confirming known associations of glycosylation with age and sex by MALDI-FTICR-MS, we report novel associations with C-reactive protein (CRP), interleukin 6 (IL-6), body mass index (BMI), leptin, adiponectin, HDL cholesterol, triglycerides (TG), insulin, gamma-glutamyl transferase (GGT), alanine aminotransferase (ALT), and smoking. Overall, the bisection, galactosylation, and sialylation of diantennary species, the sialylation of tetraantennary species, and the size of high-mannose species proved to be important plasma characteristics associated with inflammation and metabolic health.
机译:糖基化是大量的共翻译和翻译后蛋白质修饰,对蛋白质加工和活性至关重要。尽管不是模板定义的,但是糖基化确实反映了生物体的生物学状态,并且是疾病和患者分层的潜在生物标记。但是,要解释一个复杂但信息丰富的样本,例如总血浆N-糖蛋白,建立与血浆蛋白水平和全身过程的基线关联非常重要。迄今为止,已经使用色谱和电泳分离方法对血浆总N-糖基进行了大规模研究(n> 200),尽管该方法具有参考价值,但在解决血浆N-聚糖的结构复杂性方面受到限制。 MS有机会提供有关天线度,唾液酸化和高甘露糖类型物种身份的更多信息。在此,我们使用了基质辅助激光解吸/电离(MALDI)-傅立叶变换离子回旋共振(FTICR) )-MS研究来自Leiden长寿研究的2144名健康中年人的总血浆N-糖基,以便进行代谢健康和炎症标记物的关联分析。为此,将N-聚糖酶解从其蛋白质主链中释放出来,在还原端用2-氨基苯甲酸标记,然后通过负离子模式中压MALDI-FTICR-MS分析纯化。这样,我们实现了从Hex4HexNAc2到Hex7HexNAc6dHex1Neu5Ac4的61种聚糖成分的相对定量,以及由此衍生的39种糖基化特性的相对定量。在通过MALDI-FTICR-MS确认糖基化与年龄和性别的已知关联之后,我们报告了与C反应蛋白(CRP),白介素6(IL-6),体重指数(BMI),瘦素,脂联素, HDL胆固醇,甘油三酸酯(TG),胰岛素,γ-谷氨酰转移酶(GGT),丙氨酸氨基转移酶(ALT)和吸烟。总体而言,事实证明,双触角物种的平分,半乳糖基化和唾液酸化,四触角物种的唾液酸化和高甘露糖物种的大小被证明是与炎症和代谢健康相关的重要血浆特征。

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