Reversible Chemoenzymatic Labeling Strategy Enables In-depth Analysis of Protein O-GlcNAcylation
O-linked β-N-acetylglucosamine (O-GlcNAcylation), an important post-translational modification (PTM) of proteins, is involved in various biological functions.
The reversible modification of O-GlcNAc confers on-off protein functions during biological processes. Aberrations of O-GlcNAcylation are closely associated with many metabolic diseases along with the invasion and metastasis of several tumors.
Recently, a research team led by Prof. YE Mingliang and Prof. QIN Hongqiang from the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences (CAS), in collaboration with Prof. HUANG Wei from the Shanghai Institute of Materia Medica of CAS, developed a new strategy of reversible chemoenzymatic labeling of O-GlcNAc glycopeptides, which enabled the in-depth analysis of protein O-GlcNAcylation.
Their findings were published in Angew. Chem. Int. Ed. on Mar. 14.
To enable the proteome-wide analysis of O-GlcNAcylation, it is essential to selectively enrich glycopeptides from the digests of complex samples.
Many efforts have been deployed to the enrichment of O-GlcNAcylated peptides before analysis by liquid chromatography with tandem mass spectrometry (LC-MS/MS). However, most of the approaches suffer from weak binding affinity or bulky tags, which interfere with the enrichment and identification of O-GlcNAcylated peptides.
In this newly-developed strategy, the O-GlcNAc moieties were ligated with long N-glycans using an Endo-M mutant, which enabled the enrichment of the labeled glycopeptides by hydrophilic interaction liquid chromatography (HILIC). Then, the attached glycans on the enriched glycopeptides were removed by wild-type Endo-M/S to restore the O-GlcNAc moiety.
Compared with the classic chemoenzymatic labeling, this approach enabled the tag-free identification and eliminated the interference of bulky tags in glycopeptide detection.
Moreover, by using this method, the researchers identified 657 potential O-GlcNAc glycosites from only 0.4 mg of HeLa cell nuclear proteins, which was needed only 1/10 of protein samples for a comparable O-GlcNAcylation analysis, indicating the high sensitivity of this method.
Totally, they identified 1,414 glycosites from just 1.1 mg of protein samples, and 45% of them were not included in O-GlcNAcAltas of all human samples in the past 35 years, which enhanced the analysis coverage of protein O-GlcNAcylation.
The enrichment and identification of O-GlcNAcylated peptides based on the reversible chemoenzymatic labeling strategy (Image by QIN Hongqiang)
"This tag-free enrichment strategy represents a unique avenue for proteome-wide analysis of O-GlcNAcylation and promotes the mechanism studies," said Prof. YE.
The above work was supported by the National Natural Science Foundation of China, the National Key Research and Development Program of China, the Innovation Program of Science and Research of DICP, and the Youth Innovation Promotion Association of CAS. (Text by QIN Hongqiang)
