Abstract

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.

Highlights

  • We have used matrix-assisted laser desorption/ ionization (MALDI)-Fourier transform ion cyclotron resonance (FTICR)-mass spectrometry (MS) to study the total plasma N-glycome of 2144 healthy middle-aged individuals from the Leiden

  • 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

  • N-glycans were enzymatically released from their protein backbones, labeled at the reducing end with 2-aminobenzoic acid (2-AA), purified by hydrophilicinteraction liquid chromatography (HILIC)- and carbon-solid-phase extraction (SPE), and analyzed by intermediate pressure MALDI-FTICR-MS

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Summary

Introduction

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. 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. N-glycans Associate with Inflammation and Metabolic Health (ER)/Golgi localization and nucleotide sugar availability, and reflects the intricate biological state of an organism [1, 2, 12]. Observed effects in a total plasma N-glycome (TPNG), i.e. the released N-glycans from all plasma proteins, are highly informative but difficult to comprehend because of the complex contributions from relative protein glycoforms and overall glycoprotein abundances [15, 16]

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