Using micro pillar array columns (μPAC) for the analysis of permethylated glycans

Glycosylation is a complex and common post-translational modification of proteins. To study glycosylation, liquid chromatography-mass spectrometry (LC-MS) is often used to profile and structurally characterize the glycans in biological systems. While bed packed reverse phase columns are frequently utilized for the separation of permethylated glycans, the use of newly commercialized micro array pillar nanoLC columns (mu PAC) have not been demonstrated previously. Owing to its advantages such as low back pressure, reproducibility, and durability, we have investigated the viability of the mu PAC for the analysis of permethylated glycans. In this work, we demonstrate the online purification ability of mu PAC trapping column compared against PepMap trapping column. We also found that the 50 cm mu PAC can be used for the analysis of both permethylated N- and O-glycans. The use of 50 cm mu PAC was compared against the previous method. The use of 200 cm mu PAC was also investigated for the permethylated glycan analysis. 200 cm mu PAC demonstrated efficient separation of oligomannose glycan isomers as well as other complex glycans.

Automated summary

This study investigated the viability of a newly commercialized micro array pillar nanoLC columns (mu PAC) for the analysis of permethylated glycans, demonstrating its efficient separation of different types of glycans and multiple advantages.