A chemoenzymatic method for simultaneous profiling N- and O-glycans on glycoproteins using one-pot format
作者
Uriel Ortega‐Rodriguez,John Q. Bettinger,Guozhang Zou,Vincent M. Falkowski,Mari Lehtimaki,Alicia M. Matthews,Thomas G. Biel,Jordan D. Pritts,Wells W. Wu,Rong‐Fong Shen,Cyrus D. Agarabi,V. Ashutosh Rao,Hang Xie,Tongzhong Ju
Glycosylation is generally characterized and controlled as a critical quality attribute for therapeutic glycoproteins because glycans can impact protein drug-product efficacy, half-life, stability, and safety. Analytical procedures to characterize N-glycans are relatively well established, but the characterization of O-glycans is challenging due to the complex workflows and lack of enzymatic tools. Here, we present a simplified chemoenzymatic method to simultaneously profile N- and O-glycans from the same sample using a one-pot format by mass spectrometry (MS). N-glycans were first released by PNGase F, followed by O-glycopeptide generation by proteinase K, selective N-glycan reduction, and O-glycan release by β-elimination during permethylation of both N- and O-glycans. Glycan structural assignments and determination of N- to O-glycan ratio was obtained from the one-pot mass spectra. The streamlined, one-pot method is a reliable approach that will facilitate advanced characterizations for quality assessments of therapeutic glycoproteins.