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在高通量质谱筛选碳水化合物降解酶中,对一系列广泛的基质辅助激光解吸电离基质进行性能评估,以检测寡糖。

Performance evaluation on a wide set of matrix-assisted laser desorption ionization matrices for the detection of oligosaccharides in a high-throughput mass spectrometric screening of carbohydrate depolymerizing enzymes.

机构信息

INRA UR1268 Biopolymères Interactions Assemblages, Plate-Forme BIBS, F-44316 Nantes, France.

出版信息

Rapid Commun Mass Spectrom. 2011 Jul 30;25(14):2059-70. doi: 10.1002/rcm.5060.

Abstract

Compared to other analytical methods, matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) presents several unique advantages for the structural characterization of degradation products of carbohydrates. Our final goal is to implement this technique as a high-throughput platform, with the aim of exploring natural bio-diversity to discover new carbohydrate depolymerizing enzymes. In this approach, a variety of carbohydrates will be used as enzymes substrates and MALDI-MS will be employed to monitor the oligosaccharides produced. One drawback of MALDI, however, is that the choice of the matrix is largely dependent on the chemical properties of the analyte. In this context, our objective in the present work was to find the smallest set of MALDI matrices able to detect chemically heterogeneous oligosaccharides. This was done through the performance evaluation of more than 40 MALDI matrices preparations. Homogeneity of analyte-matrix deposits was considered as a critical feature, especially since the final objective is to fully automate the analyses. Evaluation of the matrices was done by means of a rigorous statistical approach. Amongst all tested compounds, our work proposes the use of the DHB/DMA ionic matrix as the most generic matrix, for rapid detection of a variety of polysaccharides including neutral, anionic, methylated, sulfated, and acetylated compounds. The selected matrices were then used to screen crude bacterial incubation media for the detection of enzymatic degradation products.

摘要

与其他分析方法相比,基质辅助激光解吸电离质谱(MALDI-MS)在碳水化合物降解产物的结构特征方面具有若干独特的优势。我们的最终目标是将该技术实现为高通量平台,旨在探索天然生物多样性以发现新的碳水化合物解聚酶。在这种方法中,将使用各种碳水化合物作为酶的底物,并采用 MALDI-MS 来监测生成的低聚糖。然而,MALDI 的一个缺点是,基质的选择在很大程度上取决于分析物的化学性质。在这种情况下,我们目前工作的目标是找到能够检测化学异构低聚糖的最小一组 MALDI 基质。这是通过对 40 多种 MALDI 基质制备物的性能评估来实现的。分析物-基质沉积物的均匀性被认为是一个关键特征,特别是因为最终目标是完全自动化分析。通过严格的统计方法来评估基质。在所有测试的化合物中,我们的工作提出使用 DHB/DMA 离子基质作为最通用的基质,用于快速检测各种多糖,包括中性、阴离子、甲基化、硫酸化和乙酰化化合物。然后,使用选定的基质来筛选粗细菌培养物的培养基,以检测酶促降解产物。

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