An Accessible Protocol for Solid-Phase Extraction of N‑Linked Glycopeptides through Reductive Amination by Amine-Functionalized Magnetic Nanoparticles

• Published in: Analytical chemistry (Washington) Vol. 85; no. 11; pp. 5535 - 5541
• Main Authors: Zhang, Ying, Kuang, Min, Zhang, Lijuan, Yang, Pengyuan, Lu, Haojie
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 04.06.2013
• Subjects: Aldehydes; Amination; Amines - chemistry; Analytical chemistry; Biological samples; blood serum; bovine serum albumin; Chemical reactions; Colorectal carcinoma; colorectal neoplasms; Colorectal Neoplasms - blood; detection limit; Extraction processes; Ferric Compounds - chemistry; glycopeptides; Glycopeptides - chemistry; Glycopeptides - isolation & purification; Glycoproteins; Glycoproteins - analysis; Glycoproteins - metabolism; Glycosylation; Humans; Magnetics; Mass Spectrometry; Nanoparticles; Nanoparticles - chemistry; Peptides; Propylamines; Proteomics; ribonucleases; Silanes - chemistry; Silicon Dioxide - chemistry; Solid Phase Extraction; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods
• ISSN: 0003-2700; 1520-6882; 1520-6882
• DOI: 10.1021/ac400733y

In light of the significance of glycosylation for wealthy biological events, it is important to prefractionate glycoproteins/glycopeptides from complex biological samples. Herein, we reported a novel protocol of solid-phase extraction of glycopeptides through a reductive amination reaction by employing the easily accessible 3-aminopropyltriethoxysilane (APTES)-functionalized magnetic nanoparticles. The amino groups from APTES, which were assembled onto the surface of the nanoparticles through a one-step silanization reaction, could conjugate with the aldehydes from oxidized glycopeptides and, therefore, completed the extraction. To the best of our knowledge, this is the first example of applying the reductive amination reaction into the isolation of glycopeptides. Due to the elimination of the desalting step, the detection limit of glycopeptides was improved by 2 orders of magnitude, compared to the traditional hydrazide chemistry-based solid phase extraction, while the extraction time was shortened to 4 h, suggesting the high sensitivity, specificity, and efficiency for the extraction of N-linked glycopeptides by this method. In the meantime, high selectivity toward glycoproteins was also observed in the separation of Ribonuclease B from the mixtures contaminated with bovine serum albumin. What’s more, this technique required significantly less sample volume, as demonstrated in the successful mapping of glycosylation of human colorectal cancer serum with the sample volume as little as 5 μL. Because of all these attractive features, we believe that the innovative protocol proposed here will shed new light on the research of glycosylation profiling.