posted on 2018-10-29, 00:00authored byRijing Liao, Yuan Gao, Ming Chen, Lulu Li, Xuye Hu
Reductive
dimethylation using formaldehyde and NaBH3CN to label peptides
or proteins on their N-termini and lysine residues
is one of the most widely used labeling methods in the quantitative
proteomics field. In this study, we characterized a ubiquitous side
reaction in dimethylation labeling, causing mass increments of 26
Da on the N-termini of peptides. It can occur extensively on most
peptides, which significantly compromises data quality in terms of
sensitivity, dynamic range, and peptide- and protein-identification
rates. Nevertheless, this side reaction was so-far overlooked, largely
because the current database search algorithms limited the detection
of unknown modifications. In order to illustrate the chemical nature
of this side reaction, 1D and 2D nuclear magnetic resonance (NMR)
was performed to elucidate the exact structure of the modification
formed through this side reaction, revealing that the side reaction
produced an N-methyl-4-imidazolidinone moiety between
the first two residues of the undesirably labeled peptides. On the
basis of the mechanism proposed for the side reaction, we optimized
the reaction conditions for dimethyl-labeling. Compared with the current
typical labeling method, our approach can dramatically suppress the
side reactions at both the standard protein and proteome levels. As
a result, with our optimal labeling method, peptide- and protein-identification
rates were significantly increased compared with those from the traditional
labeling method.