Department of Chemistry and Environmental Science, New Jersey Institute of Technology, Newark, New Jersey 07102, United States.
Department of Environmental and Plant Biology & Molecular and Cellular Biology Program, Ohio University, Athens, Ohio 45701, United States.
J Am Soc Mass Spectrom. 2020 Oct 7;31(10):2226-2235. doi: 10.1021/jasms.0c00310. Epub 2020 Sep 22.
Conventional mass spectrometry (MS)-based analytical methods for small carbohydrate fragments (oligosaccharides, degree of polymerization 2-12) are time-consuming due to the need for an offline sample pretreatment such as desalting. Herein, we report a new paper spray ionization method, named desalting paper spray (DPS), which employs a piece of triangular filter paper for both sample desalting and ionization. Unlike regular paper spray ionization (PSI) and nanoelectrospray ionization (nanoESI), DPS-MS allows fast and sensitive detection of oligosaccharides in biological samples having complex matrices (e.g., Tris, PBS, HEPES buffers, or urine). When an oligosaccharide sample is loaded onto the filter paper substrate (10 × 5 mm, height × base) made mostly of cellulose, oligosaccharides are adsorbed on the paper via hydrophilic interactions with cellulose. Salts and buffers can be washed away using an ACN/HO (90/10 ) solution, while oligosaccharides can be eluted from the paper using a solution of ACN/HO/formic acid (FA) (10/90/1 ) and directly spray-ionized from the tip of the paper. Various saccharides at trace levels (e.g., 50 fmol) in nonvolatile buffer can be quickly analyzed by DPS-MS (<5 min per sample). DPS-MS is also applicable for direct detection of oligosaccharides from glycosyltransferase (GT) reactions, a challenging task that typically requires a radioactive assay. Quantitative analysis of acceptor and product oligosaccharides shows increased product with increased GT enzymes used for the reaction, a result in line with the radioactivity assay. This work suggests that DPS-MS has potential for rapid oligosaccharide analysis from biological samples.
基于常规质谱(MS)的小分子碳水化合物片段(寡糖,聚合度 2-12)分析方法由于需要离线样品预处理(如脱盐),因此耗时较长。在此,我们报告了一种新的纸喷雾电离方法,称为脱盐纸喷雾(DPS),它使用一块三角形滤纸进行样品脱盐和电离。与常规的纸喷雾电离(PSI)和纳升电喷雾电离(nanoESI)不同,DPS-MS 允许快速灵敏地检测具有复杂基质(如 Tris、PBS、HEPES 缓冲液或尿液)的生物样品中的寡糖。当寡糖样品加载到主要由纤维素制成的滤纸基质(10×5mm,高×宽)上时,寡糖通过与纤维素的亲水相互作用吸附在纸上。盐和缓冲液可以用 ACN/HO(90/10)溶液洗掉,而寡糖可以用 ACN/HO/甲酸(FA)(10/90/1)溶液从纸上洗脱出来,并直接从纸的尖端喷雾电离。各种痕量(例如 50fmol)非挥发性缓冲液中的糖可以通过 DPS-MS 在 <5 分钟内快速分析(<5 分钟/样品)。DPS-MS 也适用于直接检测糖基转移酶(GT)反应中的寡糖,这是一项通常需要放射性测定的挑战性任务。用 GT 酶进行反应时,接受体和产物寡糖的定量分析显示产物增加,这与放射性测定结果一致。这项工作表明,DPS-MS 有可能用于从生物样品中快速分析寡糖。