Takamatsu Shinji, Korekane Hiroaki, Ohtsubo Kazuaki, Oguri Suguru, Park Jong Yi, Matsumoto Akio, Taniguchi Naoyuki
Division of Systems Glycobiology Research Group, RIKEN Global Research Cluster, Wako, Saitama, Japan.
Methods Mol Biol. 2013;1022:283-98. doi: 10.1007/978-1-62703-465-4_21.
Determining glycosyltransferase activities gives a clue for better understanding an underlying mechanism for glycomic alterations of carrier molecules. N-glycan branch formation is concertedly regulated by cooperative and competitive activities of N-acetylglucosaminyltransferases (GnTs). Here, we describe methods for large scale preparation of the oligosaccharide acceptor substrate, fluorescence-labeling of oligosaccharides by pyridylamination, quality control, and reversed phase HPLC-based measurement of GnT activities including GnT-III, IV, V, and IX.
确定糖基转移酶活性为更好地理解载体分子糖组改变的潜在机制提供了线索。N-聚糖分支的形成受到N-乙酰葡糖胺转移酶(GnTs)协同和竞争活性的协同调节。在这里,我们描述了大规模制备寡糖受体底物的方法、通过吡啶胺化对寡糖进行荧光标记、质量控制以及基于反相高效液相色谱法测量包括GnT-III、IV、V和IX在内的GnT活性的方法。