Department of Biology, University of Modena and Reggio Emilia, Modena, Italy.
Nat Protoc. 2010 Jun;5(6):993-1004. doi: 10.1038/nprot.2010.48.
Glycosaminoglycans (GAGs) have proven to be very difficult to analyze and characterize because of their high negative charge density, polydispersity and sequence heterogeneity. As the specificity of the interactions between GAGs and proteins results from the structure of these polysaccharides, an understanding of GAG structure is essential for developing a structure-activity relationship. Electrospray ionization (ESI) mass spectrometry (MS) is particularly promising for the analysis of oligosaccharides chemically or enzymatically generated by GAGs because of its relatively soft ionization capacity. Furthermore, on-line high-performance liquid chromatography (HPLC)-MS greatly enhances the characterization of complex mixtures of GAG-derived oligosaccharides, providing important structural information and affording their disaccharide composition. A detailed protocol for producing oligosaccharides from various GAGs, using controlled, specific enzymatic or chemical depolymerization, is presented, together with their HPLC separation, using volatile reversed-phase ion-pairing reagents and on-line ESI-MS structural identification. This analysis provides an oligosaccharide map together with sequence information from a reading frame beginning at the nonreducing end of the GAG chains. The preparation of oligosaccharides can be carried out in 10 h, with subsequent HPLC analysis in 1-2 h and HPLC-MS analysis taking another 2 h.
糖胺聚糖(GAGs)由于其高电荷密度、多分散性和序列异质性,已被证明非常难以分析和表征。由于 GAG 与蛋白质之间的相互作用的特异性取决于这些多糖的结构,因此了解 GAG 结构对于建立结构-活性关系至关重要。电喷雾电离(ESI)质谱(MS)因其相对软的电离能力,特别适合分析 GAG 化学或酶促产生的寡糖。此外,在线高效液相色谱(HPLC)-MS 极大地增强了对 GAG 衍生寡糖复杂混合物的表征,提供了重要的结构信息,并确定了它们的二糖组成。本文提出了一种详细的方案,使用受控的、特定的酶或化学解聚作用从各种 GAG 中产生寡糖,同时使用挥发性反相离子对试剂进行 HPLC 分离,并在线 ESI-MS 进行结构鉴定。这种分析提供了寡糖图谱以及从 GAG 链非还原端开始的阅读框的序列信息。寡糖的制备可以在 10 小时内完成,随后的 HPLC 分析需要 1-2 小时,HPLC-MS 分析还需要 2 小时。