Huang Yu, Mao Yang, Buczek-Thomas Jo Ann, Nugent Matthew A, Zaia Joseph
Center for Biomedical Mass Spectrometry, Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts, United States of America.
PLoS One. 2014 Aug 15;9(8):e105143. doi: 10.1371/journal.pone.0105143. eCollection 2014.
Sulfs are extracellular endosulfatases that selectively remove the 6-O-sulfate groups from cell surface heparan sulfate (HS) chain. By altering the sulfation at these particular sites, Sulfs function to remodel HS chains. As a result of the remodeling activity, HSulf2 regulates a multitude of cell-signaling events that depend on interactions between proteins and HS. Previous efforts to characterize the substrate specificity of human Sulfs (HSulfs) focused on the analysis of HS disaccharides and synthetic repeating units. In this study, we characterized the substrate preferences of human HSulf2 using HS oligosaccharides with various lengths and sulfation degrees from several naturally occurring HS sources by applying liquid chromatography mass spectrometry based glycomics methods. The results showed that HSulf2 preferentially digests highly sulfated HS oligosaccharides with zero acetyl groups and this preference is length dependent. In terms of length of oligosaccharides, HSulf2 digestion induced more sulfation decrease on DP6 (DP: degree of polymerization) compared to DP2, DP4 and DP8. In addition, the HSulf2 preferentially digests the oligosaccharide domain located at the non-reducing end (NRE) of the HS and heparin chain. In addition, the HSulf2 digestion products were altered only for specific isomers. HSulf2 treated NRE oligosaccharides also showed greater decrease in cell proliferation than those from internal domains of the HS chain. After further chromatographic separation, we identified the three most preferred unsaturated hexasaccharide for HSulf2.
硫酸酯酶是一种细胞外硫酸酯酶,可选择性地从细胞表面硫酸乙酰肝素(HS)链上移除6-O-硫酸基团。通过改变这些特定位点的硫酸化作用,硫酸酯酶起到重塑HS链的作用。作为重塑活性的结果,HSulf2调节众多依赖于蛋白质与HS之间相互作用的细胞信号事件。此前对人硫酸酯酶(HSulfs)底物特异性的研究主要集中在对HS二糖和合成重复单元的分析上。在本研究中,我们通过应用基于液相色谱质谱的糖组学方法,使用来自几种天然HS来源的具有不同长度和硫酸化程度的HS寡糖,对人HSulf2的底物偏好进行了表征。结果表明,HSulf2优先消化零乙酰基的高度硫酸化HS寡糖,且这种偏好具有长度依赖性。就寡糖长度而言,与DP2、DP4和DP8相比,HSulf2消化导致DP6(DP:聚合度)上的硫酸化减少更多。此外,HSulf2优先消化位于HS和肝素链非还原端(NRE)的寡糖结构域。此外,HSulf2的消化产物仅针对特定异构体发生改变。经HSulf2处理的NRE寡糖在细胞增殖方面的降低也比来自HS链内部结构域的寡糖更大。经过进一步的色谱分离,我们确定了HSulf2最偏好的三种不饱和六糖。