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Role of nitrogen lewis basicity in boronate affinity chromatography of nucleosides
Robin Tuytten1, Filip Lemière, Eddy L Esmans
1Department of Chemistry, Nucleoside Research and Mass Spectrometry Unit, and Center for Proteomics and Mass Spectrometry, University of Antwerp, Antwerp, Belgium.
Abstract:
Urinary modified nucleosides have a potential role as cancer biomarkers, and most of the methods used in their study have utilized low-pressure phenylboronate affinity chromatography materials for the purification of the cis-diol-containing nucleosides. In this study, a boronate HPLC column was surprisingly shown not to trap the nucleosides as would be expected from experience with the classic Affigel 601 resin but showed only partial selectivity toward cis-diol groups while other groups exhibited better retention. In aprotic conditions, trapping of nucleosides was possible; however, the selectivity toward cis-diol-containing compounds was lost with the Lewis basicity of available nitrogens being the main determinant of retention. The experimental findings are compared to and confirmed by DFT calculations.
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