Kinoshita A, Yamada S, Haslam S M, Morris H R, Dell A, Sugahara K
Department of Biochemistry, Kobe Pharmaceutical University, Higashinada-ku, Kobe 658-8558, Japan.
Biochemistry. 2001 Oct 23;40(42):12654-65. doi: 10.1021/bi015577n.
Squid cartilage chondroitin sulfate E (CS-E) exhibits various biological activities, including anticoagulant activities, lymphoid regulatory activities, and neuroregulatory activities [Ueoka, C., Kaneda, N., Okazaki, I., Nadanaka, S., Muramatsu, T., and Sugahara, K. (2000) J. Biol. Chem. 275, 37407-37413]. These activities are expressed through molecular interactions with specific proteins, including heparin cofactor II, selectins, CD44, chemokines, and the heparin-binding growth factor midkine. Hence, the sugar sequence information is essential for a better understanding of the CS-E functions. Previously, several novel tetrasaccharides containing the unreported 3-O-sulfated glucuronic acid (GlcA) were isolated after digestion of squid cartilage CS-E with testicular hyaluronidase. In this study, hexasaccharides were isolated to obtain more detailed sequence information, especially around the GlcA(3-O-sulfate) residue, and were characterized by fast atom bombardment mass spectrometry and 500 or 600 MHz (1)H NMR spectroscopy. The findings demonstrate one tetrasulfated and five pentasulfated hexasaccharide sequences, five of them being novel. They were composed of three disaccharide building units of either A [GlcA(beta1-3)GalNAc(4-O-sulfate)], E [GlcA(beta1-3)GalNAc(4,6-O-disulfate)], K [GlcA(3-O-sulfate)(beta1-3)GalNAc(4-O-sulfate)], L [GlcA(3-O-sulfate)(beta1-3)GalNAc(6-O-sulfate)], or M [GlcA(3-O-sulfate)(beta1-3)GalNAc(4,6-O-disulfate)], forming E-A-A, M-A-A, K-L-A, E-E-A, K-K-A, and A-M-A hexasaccharide sequences. The K-L tetrasaccharide sequence is to date unreported. The isolated sequences appear to indicate the occurrence of an unreported GlcA 3-O-sulfotransferase specific for chondroitin sulfate. The obtained sequence information will be useful for investigating the structure-function relationship and biosynthesis of CS-E.
鱿鱼软骨硫酸软骨素E(CS-E)具有多种生物活性,包括抗凝血活性、淋巴调节活性和神经调节活性[上冈,C.,金田,N.,冈崎,I.,稻田中,S.,村松,T.,和菅原,K.(2000)《生物化学杂志》275,37407 - 37413]。这些活性是通过与特定蛋白质的分子相互作用来表达的,这些蛋白质包括肝素辅因子II、选择素、CD44、趋化因子和肝素结合生长因子中期因子。因此,糖序列信息对于更好地理解CS-E的功能至关重要。此前,在用睾丸透明质酸酶消化鱿鱼软骨CS-E后,分离出了几种含有未报道的3-O-硫酸化葡萄糖醛酸(GlcA)的新型四糖。在本研究中,分离出六糖以获得更详细的序列信息,特别是围绕GlcA(3-O-硫酸盐)残基的信息,并通过快原子轰击质谱和500或600 MHz的(1)H NMR光谱进行表征。研究结果表明了一种四硫酸化和五种五硫酸化的六糖序列,其中五种是新的。它们由A [GlcA(β1-3)GalNAc(4-O-硫酸盐)]、E [GlcA(β1-3)GalNAc(4,6-O-二硫酸盐)]、K [GlcA(3-O-硫酸盐)(β1-3)GalNAc(4-O-硫酸盐)]、L [GlcA(3-O-硫酸盐)(β1-3)GalNAc(6-O-硫酸盐)]或M [GlcA(3-O-硫酸盐)(β1-3)GalNAc(4,6-O-二硫酸盐)]这三种二糖构建单元组成,形成E-A-A、M-A-A、K-L-A、E-E-A、K-K-A和A-M-A六糖序列。K-L四糖序列迄今为止尚未见报道。分离出的序列似乎表明存在一种未报道的对硫酸软骨素具有特异性的GlcA 3-O-磺基转移酶。获得的序列信息将有助于研究CS-E的结构-功能关系和生物合成。