Label-Free Discovery Array Platform for the Characterization of Glycan Binding Proteins and Glycoproteins

被引:17
|
作者
Gray, Christopher J. [1 ,2 ]
Sanchez-Ruiz, Antonio [1 ,2 ]
Sardzikova, Ivana [1 ,2 ]
Ahmed, Yassir A. [3 ]
Miller, Rebecca L. [3 ]
Reyes Martinez, Juana E. [4 ]
Pallister, Edward [1 ,2 ]
Huang, Kun [1 ,2 ]
Both, Peter [1 ,2 ]
Hartmann, Mirja [1 ,2 ,5 ]
Roberts, Hannah N. [1 ,2 ]
Sardzik, Robert [1 ,2 ,6 ]
Mandal, Santanu [1 ,2 ]
Turnbull, Jerry E. [3 ]
Eyers, Claire E. [3 ]
Flitsch, Sabine L. [1 ,2 ]
机构
[1] Univ Manchester, Sch Chem, 131 Princess St, Manchester M1 7DN, Lancs, England
[2] Univ Manchester, Manchester Inst Biotechnol, 131 Princess St, Manchester M1 7DN, Lancs, England
[3] Univ Liverpool, Inst Integrat Biol, Dept Chem, Crown St, Liverpool L69 7ZB, Merseyside, England
[4] Univ Guanajuato, Div Ciencias Natur & Exactas, Dept Biol, Col Noria Alta S-N, Guanajuato 36050, Mexico
[5] Chem Cluster Bayern GmbH, Munich, Germany
[6] Syngenta, Cambridge, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
SELF-ASSEMBLED MONOLAYERS; MASS-SPECTROMETRY; CARBOHYDRATE MICROARRAYS; LECTIN MICROARRAY; GOLD SURFACES; HUMAN-MILK; N-GLYCANS; OLIGOSACCHARIDES; GLYCOSYLATION; HEPARIN;
D O I
10.1021/acs.analchem.6b04122
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The identification of carbohydrate protein interactions is central to our understanding of the roles of cell surface carbohydrates (the glycocalyx), fundamental for cell recognition events. Therefore, there is a need for fast high-throughput biochemical tools to capture the complexity of these biological interactions. Here, we describe a rapid method for qualitative label-free detection of carbohydrate-protein interactions on arrays of simple synthetic glycans, more complex natural glycosaminoglycans (GAG), and lectins/carbohydrate binding proteins using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. The platform can unequivocally identify proteins that are captured from either purified or complex sample mixtures, including biofluids. Identification of proteins bound to the functionalized array is achieved by analyzing either the intact protein mass or, after on-chip proteolytic digestion, the peptide mass fingerprint and/or tandem mass spectrometry of selected peptides, which can yield highly diagnostic sequence information. The platform described here should be a valuable addition to the limited analytical toolbox that is currently available for glycomics.
引用
收藏
页码:4444 / 4451
页数:8
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