Analysis of the N-acetylneuraminic acid and N-glycolylneuraminic acid contents of glycoproteins by high-pH anion-exchange chromatography with pulsed amperometric detection (HPAEC/PAD)

• Published in: Glycobiology (Oxford) Vol. 8; no. 1; pp. 35 - 43
• Main Authors: Rohrer, Jeffrey S., Thayer, Jim, Weitzhandler, Michael, Avdalovic, Nebojsa
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.01.1998
• Subjects: Animals; Cattle; Chromatography, Ion Exchange - methods; Chromatography, Ion Exchange - standards; Chromatography, Ion Exchange - statistics & numerical data; Electrochemistry; Electrodes; Glycoproteins - chemistry; high-pH anion-exchange chromatography; Humans; Hydrogen-Ion Concentration; N-acetylneuraminic acid; N-Acetylneuraminic Acid - analysis; N-glycolylneuraminic acid; Neuraminic Acids - analysis; pulsed amperometric detection; Reference Standards; Reproducibility of Results; Sensitivity and Specificity; sialic acids
• ISSN: 0959-6658; 1460-2423
• DOI: 10.1093/glycob/8.1.35

Presence or absence of N-acetylneuraminic acid (Neu5Ac) can change a sialylated glycoprotein's serum half-life and possibly its function. We evaluated the linearity, sensitivity, reproducibility, and accuracy of a HPAEC/PAD method to determine its suitability for routine simultaneous analysis of Neu5Ac and N-glycolylneuraminic acid (Neu5Gc). An effective internal standard for this analysis is 3-deoxy-d-glycerod-galacto-2-nonulosonic acid (KDN). We investigated the effect of the Au working electrode recession and determined that linear range and sensitivity were dependent on electrode recession. Using an electrode that was 350 mm recessed from the electrode block, the minimum detection limits of Neu5Ac, KDN, and Neu5Gc were 2, 5, and 2 pmol, respectively, and were reduced to 1, 2, and 0.5 pmol using a new electrode. The response of standards was linear from 10 to 500 pmol (r2 > 0.99) regardless of electrode recession. When Neu5Ac, KDN, and Neu5Gc (200 pmol each) were analyzed repetitively for 48 h, area RSDs were <3%. Reproducibility was unaffected when injections of glycoprotein neuraminidase and acid digestions were interspersed with standard injections. Area RSDs of Neu5Ac and Neu5Gc improved when the internal standard was used. We determined the precision and accuracy of this method for both a recessed and a new working electrode by analyzing Neu5Ac and Neu5Gc contents of bovine fetuin and bovine and human transferrins. Results were consistent with published values and independent of the working electrode. The sensitivity, reproducibility, and accuracy of this method make it suitable for direct routine analysis of glycoprotein Neu5Ac and Neu5Gc contents.