Ziegler C, Mersmann G
Biochim Biophys Acta. 1984 Jun 29;799(3):203-8. doi: 10.1016/0304-4165(84)90262-9.
The structural similarity of the inner core of complex-type prosthetic oligosaccharides of N-asparagine glycoproteins and of the linkage region between the polysaccharide part and the protein chain of cornea proteokeratan sulfate makes their biosynthesis via a common route an attractive hypothesis. To test this, a tissue culture system was established to determine the rate of proteokeratan sulfate biosynthesis in bovine cornea and to measure the influence of several effectors of the dolichol pathway on this rate. Addition of dolichyl phosphate enhanced the formation of proteokeratan sulfate. Tunicamycin, 2-deoxy-D-glucose, bromoconduritol and deoxynojirimycin inhibited this process. Swainsonine probably led to the formation of a keratan sulfate with hybrid structure. The results support that the linkage region of cornea proteokeratan sulfate is synthesized via the assembly of a glucosylated dolichyl pyrophosphoryl oligosaccharide, its transfer to protein and subsequent processing by glycosidases.
N-天冬酰胺糖蛋白的复合型寡糖假体的内核与角膜蛋白角质硫酸盐的多糖部分和蛋白质链之间的连接区域的结构相似性,使得通过共同途径进行生物合成这一假说颇具吸引力。为了验证这一点,建立了一个组织培养系统,以确定牛角膜中蛋白角质硫酸盐的生物合成速率,并测量多萜醇途径的几种效应物对该速率的影响。添加磷酸多萜醇可增强蛋白角质硫酸盐的形成。衣霉素、2-脱氧-D-葡萄糖、溴制霉菌醇和脱氧野尻霉素抑制了这一过程。苦马豆素可能导致形成具有杂合结构的硫酸角质素。结果支持角膜蛋白角质硫酸盐的连接区域是通过糖基化的多萜醇焦磷酸寡糖的组装、其向蛋白质的转移以及随后糖苷酶的加工来合成的。