Harvey David J, Baruah Kavitha, Scanlan Christopher N
Oxford Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford, UK.
J Mass Spectrom. 2009 Jan;44(1):50-60. doi: 10.1002/jms.1470.
Structures of N-glycans released from rat CEACAM1 expressed in human embryonic kidney cells were determined by MALDI and negative ion nanospray MS/MS techniques. The major carbohydrates were bi-, tri- and tetra-antennary complex glycans with and without sialic acid, fucose and bisecting GlcNAc residues. High-mannose glycans, predominantly Man(5)GlcNAc(2), were also found. The negative ion fragmentation technique easily identified the branching pattern of the triantennary glycans (mainly branched on the 6-antenna) and the presence of 'bisecting' GlcNAc residues (attached to the 4-position of the core mannose), features that are difficult to determine by traditional techniques. Sialic acids were in both alpha2-3 and alpha2-6 linkage as determined by MALDI-TOF MS following linkage-specific derivatization.
通过基质辅助激光解吸电离(MALDI)和负离子纳米喷雾串联质谱(MS/MS)技术,确定了在人胚肾细胞中表达的大鼠癌胚抗原相关细胞黏附分子1(CEACAM1)释放的N-聚糖结构。主要碳水化合物是带有和不带有唾液酸、岩藻糖和平分型N-乙酰葡糖胺(GlcNAc)残基的二天线、三天线和四天线复合聚糖。还发现了高甘露糖型聚糖,主要是Man(5)GlcNAc(2)。负离子碎裂技术能够轻松识别三天线聚糖的分支模式(主要在6-天线分支)以及“平分型”GlcNAc残基的存在(连接到核心甘露糖的4位),而这些特征用传统技术很难确定。通过连接特异性衍生化后的MALDI-TOF MS测定,唾液酸以α2-3和α2-6两种连接方式存在。