Department of Chemistry, Indiana University, 800 E. Kirkwood Ave., Bloomington, IN, 47405, USA.
J Am Soc Mass Spectrom. 2018 Jun;29(6):1125-1137. doi: 10.1007/s13361-018-1933-y. Epub 2018 May 9.
Glycoconjugates are directly or indirectly involved in many biological processes. Due to their complex structures, the structural elucidation of glycans and the exploration of their role in biological systems have been challenging. Glycan pools generated through release from glycoprotein or glycolipid mixtures can often be very complex. For the sake of procedural simplicity, many glycan profiling studies choose to concentrate on a single class of glycoconjugates. In this paper, we demonstrate it feasible to cover glycosphingolipids, N-glycans, and O-glycans isolated from the same sample. Small volumes of human blood serum and ascites fluid as well as small mouse brain tissue samples are sufficient to profile sequentially glycans from all three classes of glycoconjugates and even positively identify some mixture components through MALDI-MS and LC-ESI-MS. The results show that comprehensive glycan profiles can be obtained from the equivalent of 500-μg protein starting material or possibly less. These methodological improvements can help accelerating future glycomic comprehensive studies, especially for precious clinical samples. Graphical Abstract Outline of glycan profiling procedures.
糖缀合物直接或间接地参与许多生物过程。由于其结构复杂,糖链的结构阐明和对其在生物系统中作用的探索一直具有挑战性。通过从糖蛋白或糖脂混合物中释放产生的糖库通常非常复杂。为了程序简单起见,许多聚糖分析研究选择集中于单一类型的糖缀合物。本文中,我们证明了从同一样品中分离出的糖鞘脂、N-聚糖和 O-聚糖进行分析是可行的。少量的人血清和腹水以及小的鼠脑组织样本足以对所有三种类型的糖缀合物的聚糖进行顺序分析,甚至可以通过 MALDI-MS 和 LC-ESI-MS 对某些混合物成分进行阳性鉴定。结果表明,从相当于 500μg 蛋白质起始材料或可能更少的量中可以获得综合的聚糖图谱。这些方法学的改进有助于加速未来的糖组学综合研究,特别是对于珍贵的临床样本。