Institute for Biology and Biotechnology of Plants, University of Münster , Schlossplatz 8, 48143 Münster, Germany.
Institute for Organic Chemistry, University of Münster , Corrensstraße 40, 48149 Münster, Germany.
Anal Chem. 2017 Mar 7;89(5):2893-2900. doi: 10.1021/acs.analchem.6b04183. Epub 2017 Feb 13.
Partially acetylated chito-oligosaccharides (paCOS) have diverse bioactivities that turn them into promising compounds especially for medical and agricultural applications. These properties likely arise from different acetylation patterns, but determining the sequences of paCOS and producing paCOS with patterns of interest have proven difficult. We present a novel method for sequencing submicrogram amounts of paCOS using quantitative mass spectrometry, allowing one to rapidly analyze the substrate specificities of chitosan hydrolases that can be used to produce paCOS. The method involves four major steps: (i) acetylation of free amino groups in paCOS using a deuterated reagent; (ii) labeling the reducing end with an O-tag; (iii) quantifying paCOS using [C, H]-labeled isotopologs as internal standards; (iv) sequencing paCOS by tandem MS. Eventually, this method will aid in developing enzymes with cleavage patterns optimized for producing paCOS with defined patterns of acetylation and specific bioactivities.
部分乙酰化壳寡糖(paCOS)具有多种生物活性,使它们成为有前途的化合物,特别是在医学和农业应用方面。这些特性可能源于不同的乙酰化模式,但确定 paCOS 的序列并产生具有所需模式的 paCOS 一直很困难。我们提出了一种使用定量质谱法对亚微克量的 paCOS 进行测序的新方法,允许人们快速分析可用于生产 paCOS 的壳聚糖水解酶的底物特异性。该方法包括四个主要步骤:(i)使用氘代试剂乙酰化 paCOS 中的游离氨基;(ii)用 O 标记物标记还原端;(iii)使用 [C,H]-标记的同位素作为内标定量 paCOS;(iv)通过串联质谱测序 paCOS。最终,这种方法将有助于开发具有优化切割模式的酶,以产生具有定义乙酰化模式和特定生物活性的 paCOS。