From Fringe to the Mainstream: How ETD MS Brought O-GlcNAc to the Masses

被引:0
|
作者
Udeshi, Namrata D. [1 ]
Hart, Gerald W. [2 ]
Slawson, Chad [3 ]
机构
[1] Broad Inst MIT & Harvard Univ, Cambridge, MA 02142 USA
[2] Univ Georgia, CCRC, Dept Biochem & Mol Biol, Athens, GA USA
[3] Univ Kansas, Med Ctr, Dept Biochem, Kansas City, KS 66160 USA
关键词
LINKED N-ACETYLGLUCOSAMINE; GLCNACYLATION SITES; PROTEIN; DISSOCIATION; SPECTROMETRY; IDENTIFICATION; GLYCOPEPTIDES; EXPRESSION;
D O I
10.1016/j.mcpro.2024.100859
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
O-GlcNAcylation was identified in the 1980s by Torres and Hart and modifies thousands of cellular proteins, yet the regulatory role of O-GlcNAc is still poorly understood compared to the abundance of mechanistic information known for other cycling post-translational modifications like phosphorylation. Many challenges are associated with studying O-GlcNAcylation and are tied to the technical hurdles with analysis by mass spectrometry. Over the years, many research groups have developed important methods to study O-GlcNAcylation revealing its role in the cell, and this perspective aims to review the challenges and innovations around O-GlcNAc research and chronicle the work by Donald F. Hunt and his laboratory, particularly in development of ETD and its application to this field of research.
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页数:5
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