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Improved de novo sequencing of heparin/heparan sulfate oligosaccharides by propionylation of sites of sulfation

机译:通过硫化位点的丙酰化改善肝素/硫酸乙酰肝素硫酸寡糖的Nevo测序

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The structure of heparin and heparan sulfate (Hep/HS) oligosaccharides, as determined by the length and the pattern of sulfation, acetylation, and uronic acid epimerization, dictates their biological function through modulating interactions with protein targets. But fine structural determination is a very challenging task due to the lability of the sulfate modifications and difficulties in separating isomeric HS chains. Previously, we reported a strategy for chemical derivatization involving permethylation, desulfation, and trideuteroperacetylation, combined with standard reverse phase LC-MS/MS that enables the structural sequencing for heparin/HS oligosaccharides of sizes up to dodecasaccharide by positionally replacing all sulfates with more stable trideuteroacetyl groups, allowing for robust MS/MS sequencing. However, isomeric oligosaccharides that contain both N-sulfation and N-acetylation become isotopomers after labeling, differing only in the sites of deuteration. This prevents chromatographic separation of these different mixed domain sequences post-derivatization, and makes sequencing by MS/MS difficult due to co-fragmentation of the isotopomers leading to chimeric product ion spectra. In order to improve chromatographic separation of mixed domain oligosaccharides, we have introduced a propionylation step in place of trideuteroacetylation for labeling of sites of sulfation. HS standard disaccharides have been used to evaluate the efficiency of this improved chemical derivatization. The results show that we can quantitatively replace sulfation with propionyl groups with the same high efficiency as the previously reported trideuteroacetylation. After derivatization, we demonstrate the ability to chromatographically separate two mixed domain tetrasaccharide isomers differing solely by the order of N-sulfation and N-acetylation, allowing for full sequencing of each by MS/MS. These results represent a marked improvement in the ability of our previously reported
机译:肝素和硫酸乙酰肝素(HEP / HS)寡糖的结构,由硫化,乙酰化和助核酸差异的长度和图案测定,通过调节与蛋白质靶标的相互作用来决定它们的生物学功能。但是,由于硫酸盐修饰的可易令和分离异构HS链中的困难,细结构测定是一个非常具有挑战性的任务。此前,我们报告了涉及渗透偏差,脱硫和三相管酰基化的化学衍生化的策略,与标准反相LC-MS / MS联合,使得通过定位替代所有硫酸盐,可以通过定位替代所有硫酸糖的肝素/ HS寡糖的结构测序。三氘基因基,允许鲁棒MS / MS测序。然而,含有N-硫化和N-乙酰化的异构寡糖在标记后变成同位素,仅在氘的位点不同。这防止了这些不同的混合结构域序列的色谱分离后衍生化,并且由于在导致嵌合产物离子光谱的同位素的共分碎片而使MS / MS进行测序。为了改善混合结构域低聚糖的色谱分离,我们已经引入了丙酰化步骤代替TrideOrateRyalateLath化以标记硫化位点。 HS标准二糖已被用于评估这种改进的化学衍生化的效率。结果表明,我们可以用与先前报道的三水晶酰基化相同的高效率定量取代硫酸硫化。在衍生化之后,我们证明了通过N-硫化和N-乙酰化的顺序分离间隔分离的两个混合域四糖异构体的能力,允许通过MS / MS进行全部测序。这些结果表示我们先前报告的能力的显着改善

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