Chemical conjugation to differentiate monosaccharides by Raman and surface enhanced Raman spectroscopy

被引:5
|
作者
Schorr, Hannah C. [1 ]
Schultz, Zachary D. [1 ]
机构
[1] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
MASS-SPECTROMETRY; BORONIC ACID; SERUM GLYCOPROTEINS; GLUCOSE; ORIENTATION; SPECTRA; PROTEIN; COMPLEXES; PROGRESS; CANCER;
D O I
10.1039/d2an01762h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Sugars play important roles in numerous biological processes, from providing energy to modifying proteins to alter their function. Glycosylation, the attachment of a sugar residue to a protein, is the most common post translational modification. Identifying the glycans on a protein is a useful tool both for pharmaceutical development as well as probing the proteome and glycome further. Sugars, however, are difficult analytes to probe due to their isomeric nature. In this work, Raman spectroscopy and surface enhanced Raman spectroscopy (SERS) are used to identify different monosaccharide species based on the vibrational modes of these isomeric analytes. The weak scattering of the sugars was overcome through conjugation with phenylboronic acid to provide a larger Raman scattering cross section and induce slight changes in the observed spectra associated with the structure of the monosaccharides. Spontaneous Raman, SERS in flow, and static SERS detection were performed in order to discriminate between arabinose, fructose, galactose, glucose, mannose, and ribose, as well as provide a method for identification and quantification for these sugar conjugates.
引用
收藏
页码:2035 / 2044
页数:10
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