Stable isotope labeling differential glycans discovery in the serum of acute myocardial infarction by ultrahigh-performance liquid chromatography-quadrupole-Orbitrap high resolution mass spectrometry

• Published in: Analytica chimica acta Vol. 1264; p. 341269
• Main Authors: Li, Xi-Ling, Li, Yuxuan, Xiao, Shuyun, Li, Qingsong, Han, Chengqiang, Liu, Danyang, Cui, Tengfei, Rao, Xiyang, Todoroki, Kenichiro, Yang, Guang, Min, Jun Zhe
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 11.07.2023
• Subjects: Acute myocardial infarction; Biomarkers; Chromatography, High Pressure Liquid - methods; Chromatography, Liquid; Glycan biomarkers; Humans; Isotope Labeling - methods; Mass Spectrometry - methods; Polysaccharides - analysis; Pronase E; Stable isotope labeling; UHPLC-HRMS; Pronase E; Stable isotope labeling; UHPLC-HRMS; Acute myocardial infarction; Glycan biomarkers
• ISSN: 0003-2670; 1873-4324
• DOI: 10.1016/j.aca.2023.341269

Acute myocardial infarction (AMI) poses a grave threat to human life. However, most clinical biomarkers have limitations of low sensitivity and specificity. Therefore, screening novel glycan biomarkers with high sensitivity and specificity is crucial for the prevention and treatment of AMI. The novel method of ultrahigh-performance liquid chromatography coupled to quadrupole-Orbitrap high-resolution mass spectrometry (UHPLC-Q-Orbitrap HRMS) with d0/d5-BOTC probe labeling for relative quantification of glycans based on Pronase E digestion was established to screen novel glycan biomarkers in the serum of 34 AMI patients relative to healthy volunteers. The monosaccharide model D-glucosamine was used to investigate the effectiveness of the derivatization; the limit of detection (S/N = 3) was 10 amol. The accuracy was verified based on the consistency of different theoretical molar ratios (d0/d5 = 1:2, 2:1) and intensity ratios following digestion of glycoprotein ribonuclease B. Expressions of H4N4F3SA, H4N6F2, H4N6SA, H4N6F3 and H5N4FSA in the serum were significantly different (p < 0.0005) between AMI patients and healthy volunteers. The area under the receiver operating characteristic curve (AUC) for H4N6SA, H5N4FSA, and H4N6F2 was greater than 0.9039. Based on the proposed method, H4N6SA, H5N4FSA, and H4N6F2 in human serum showed high accuracy and specificity and may serve as potential glycan biomarkers, crucial for the diagnosis and treatment monitoring of AMI. [Display omitted] •A novel UHPLC-HRMS method for differential glycan in human serum was developed.•14 glycans were identified using the relative quantification method in AMI serum.•Bi-antennary different degree of core fucosylated and sialylated glycans were detected.•Four high specificity glycan biomarkers provide possibility for pre-warning of AMI.