Enhancing glycan isomer separations with metal ions and positive and negative polarity ion mobility spectrometry-mass spectrometry analyses

被引:0
作者
Xueyun Zheng
Xing Zhang
Nathaniel S. Schocker
Ryan S. Renslow
Daniel J. Orton
Jamal Khamsi
Roger A. Ashmus
Igor C. Almeida
Keqi Tang
Catherine E. Costello
Richard D. Smith
Katja Michael
Erin S. Baker
机构
[1] Earth and Biological Sciences Directorate,Skaggs School of Pharmacy and Pharmaceutical Sciences, Anschutz Medical Campus
[2] Pacific Northwest National Laboratory,Department of Chemistry and Border Biomedical Research Center
[3] University of Colorado,Department of Biological Sciences and Border Biomedical Research Center
[4] University of Texas at El Paso,Center for Biomedical Mass Spectrometry
[5] University of Texas at El Paso,undefined
[6] Boston University School of Medicine,undefined
来源
Analytical and Bioanalytical Chemistry | 2017年 / 409卷
关键词
Ion mobility spectrometry; Mass spectrometry; Glycans; -Glycans; Isomers;
D O I
暂无
中图分类号
学科分类号
摘要
Glycomics has become an increasingly important field of research since glycans play critical roles in biology processes ranging from molecular recognition and signaling to cellular communication. Glycans often conjugate with other biomolecules, such as proteins and lipids, and alter their properties and functions, so glycan characterization is essential for understanding the effects they have on cellular systems. However, the analysis of glycans is extremely difficult due to their complexity and structural diversity (i.e., the number and identity of monomer units, and configuration of their glycosidic linkages and connectivities). In this work, we coupled ion mobility spectrometry with mass spectrometry (IMS-MS) to characterize glycan standards and biologically important isomers of synthetic αGal-containing O-glycans including glycotopes of the protozoan parasite Trypanosoma cruzi, which is the causative agent of Chagas disease. IMS-MS results showed significant differences for the glycan structural isomers when analyzed in positive and negative polarity and complexed with different metal cations. These results suggest that specific metal ions or ion polarities could be used to target and baseline separate glycan isomers of interest with IMS-MS.
引用
收藏
页码:467 / 476
页数:9
相关论文
共 178 条
[1]  
Raman R(2005)Glycomics: an integrated systems approach to structure-function relationships of glycans Nat Methods 2 817-24
[2]  
Raguram S(2004)Glycomics: a pathway to a class of new and improved therapeutics Nat Rev Drug Discov 3 863-73
[3]  
Venkataraman G(2004)Glycans and neural cell interactions Nat Rev Neurosci 5 195-208
[4]  
Paulson JC(2004)Role of glycosylation in development Annu Rev Biochem 73 491-537
[5]  
Sasisekharan R(2002)Protein glycosylation: nature, distribution, enzymatic formation, and disease implications of glycopeptide bonds Glycobiology 12 43R-56
[6]  
Shriver Z(1993)Biological roles of oligosaccharides: all of the theories are correct Glycobiology 3 97-130
[7]  
Raguram S(2007)N-glycan structure dictates extension of protein folding or onset of disposal Nat Chem Biol 3 313-20
[8]  
Sasisekharan R(2006)Genetic defects in the human glycome Nat Rev Genet 7 537-51
[9]  
Kleene R(1994)Lytic anti-α-galactosyl antibodies from patients with chronic Chagas’ disease recognize novel O-linked oligosaccharides on mucin-like glycosyl-phosphatidylinositol-anchored glycoproteins of Trypanosoma cruzi Biochem J 304 793-802
[10]  
Schachner M(1991)Direct lysis of Trypanosoma cruzi: a novel effector mechanism of protection mediated by human anti-gal antibodies Parasite Immunol 13 345-56