Turnbull J E, Gallagher J T
Department of Clinical Research, University of Manchester Christie Hospital and Holt Radium Institute, U.K.
Biochem J. 1991 Jul 15;277 ( Pt 2)(Pt 2):297-303. doi: 10.1042/bj2770297.
A strategy that we originally used to identify an N-acetylated domain adjacent to the protein-linkage sequence of heparan sulphate proteoglycan (HSPG) [Lyon, Steward, Hampson & Gallagher (1987) Biochem. J. 242, 493-498] has been adapted for analysis of the location of GlcNSO3-HexA and GlcNSO3(+/- 6S)-IdoA(2S) units most proximal to the core protein. [3H]Glucosamine-labelled HSPG from human skin fibroblasts was depolymerized by using HNO2 or heparinase under conditions that allowed cleavage of all susceptible linkages. The degraded PG was coupled to Sepharose beads through the protein component, enabling specific recovery of protein-linked resistant oligosaccharides. These were released by treatment with alkaline borohydride and analysed by gel filtration and gradient PAGE. This strategy allowed investigation of the sequence of sugar residues along the chain relative to a common reference point (i.e. the reducing end of the chain). HNO2 scission confirmed the presence of a well-defined N-acetylated sequence predominantly 9-12 disaccharide units in length proximal to the core protein. Heparinase scission produced two classes of oligosaccharides (Mr approx. 7000 and 15,000) with the general formula: IdoA(2S)-GlcNSO3-[HexA-GlcNR]n-HexA-GlcNSO3-[Hex A-GlcNAc]9 12-GlcA-Gal-Gal-Xyl in which the average value for n is 1-2 for the 7000-Mr species and approx. 22 for the 15,000-Mr species. The latter oligosaccharides extend to about one-third of the total length of the HS chains (Mr approx. 45,000). HNO2 scission of these oligosaccharides enabled hypothetical models for their sequence to be proposed. The general arrangement of N-sulphated and N-acetylated disaccharides between the proximal GlcNSO3 and terminal IdoA(2S) residues of the 15,000-Mr fragment was similar to that in the original polysaccharide, suggesting the possibility of a tandemly repeating pattern in the sequence of HS.
我们最初用于鉴定硫酸乙酰肝素蛋白聚糖(HSPG)蛋白连接序列附近的N - 乙酰化结构域的策略[Lyon、Steward、Hampson和Gallagher(1987年),《生物化学杂志》242卷,493 - 498页]已被改编用于分析最靠近核心蛋白的GlcNSO3 - HexA和GlcNSO3(+/- 6S)-IdoA(2S)单元的位置。用人皮肤成纤维细胞的[³H]葡糖胺标记的HSPG在允许切割所有敏感连接的条件下,通过使用亚硝酸或肝素酶使其解聚。降解的蛋白聚糖通过蛋白质成分与琼脂糖珠偶联,从而能够特异性回收与蛋白质连接的抗性寡糖。通过用碱性硼氢化钠处理释放这些寡糖,并通过凝胶过滤和梯度聚丙烯酰胺凝胶电泳进行分析。该策略允许相对于一个共同的参考点(即链的还原端)研究沿链的糖残基序列。亚硝酸切割证实了在靠近核心蛋白处存在一个明确的N - 乙酰化序列,其长度主要为9 - 12个二糖单元。肝素酶切割产生了两类寡糖(分子量约为7000和15000),其通式为:IdoA(2S)-GlcNSO3-[HexA - GlcNR]n - HexA - GlcNSO3-[Hex A - GlcNAc]9 - 12 - GlcA - Gal - Gal - Xyl,其中对于分子量为7000的物种,n的平均值为1 - 2,对于分子量为15000的物种,n约为22。后一类寡糖延伸至HS链总长度的约三分之一(分子量约为45000)。对这些寡糖进行亚硝酸切割使得能够提出其序列的假设模型。在分子量为15000的片段的近端GlcNSO3和末端IdoA(2S)残基之间,N - 硫酸化和N - 乙酰化二糖的总体排列与原始多糖中的相似,这表明HS序列中可能存在串联重复模式。