Yang M, Butler M
Department of Microbiology, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada.
Biotechnol Prog. 2000 Sep-Oct;16(5):751-9. doi: 10.1021/bp000090b.
Recombinant human erythropoietin (EPO) was produced by a stable transfected CHO-K1 cell clone (EPO-81) grown in serum-free medium. Our previous work showed that there was a significant increase in the heterogeneity of the glycoforms of EPO and a reduction of the sialylation at 20 mM NH(4)Cl. In the work presented here, the effects of ammonia on EPO N-linked oligosaccharides were analyzed. EPO was purified from culture supernatants by immunoaffinity chromatography. The N-linked oligosaccharides were released enzymatically and analyzed by fluorophore-assisted carbohydrate electrophoresis (FACE) and HPLC. The FACE N-linked oligosaccharide profile showed that the sialylated glycans contain one prominent band at a position corresponding to eight glucose units. The density of the major band was greatly diminished and the width was significantly increased in cultures containing added ammonia. The proportion of tetraantennary structures was reduced by 60%, while the tri- and biantennary structures were increased proportionally in the presence of ammonia. Glycan analysis by HPLC using a weak anion exchange column showed that the most significant characteristic effect of ammonia was a reduction of the proportion of glycans with four sialic acids from 46% in control cultures to 29% in ammonia-treated cultures. Analysis of the desialylated glycans by normal phase chromatography indicated a distribution of tetra-, tri-, and biantennary structures similar to that shown by FACE. The N-linked glycan sequence was determined by sequential exoglycosidase digestion followed by FACE. The results indicated a typical N-linked complex oligosaccharide structure. Glycans from ammonia-containing cultures showed the same sequence pattern. In conclusion, we showed that ammonia in the culture medium affected EPO glycosylation, which was observed as a reduction of the tetraantennary and tetrasialylated oligosaccharide structures. However, the presence of ammonia in the cultures did not change the oligosaccharide sequence.
重组人促红细胞生成素(EPO)由在无血清培养基中生长的稳定转染CHO - K1细胞克隆(EPO - 81)产生。我们之前的研究表明,在20 mM NH₄Cl条件下,EPO糖型的异质性显著增加,唾液酸化程度降低。在本研究中,分析了氨对EPO N - 连接寡糖的影响。通过免疫亲和色谱从培养上清液中纯化EPO。通过酶法释放N - 连接寡糖,并采用荧光辅助碳水化合物电泳(FACE)和高效液相色谱(HPLC)进行分析。FACE N - 连接寡糖图谱显示,唾液酸化聚糖在对应于八个葡萄糖单位的位置有一条明显的条带。在添加氨的培养物中,主要条带的密度大大降低,宽度显著增加。四天线结构的比例降低了60%,而在有氨存在的情况下,三天线和双天线结构成比例增加。使用弱阴离子交换柱的HPLC糖链分析表明,氨最显著的特征效应是含有四个唾液酸的聚糖比例从对照培养物中的46%降至氨处理培养物中的29%。通过正相色谱分析去唾液酸化聚糖表明,其四天线、三天线和双天线结构的分布与FACE所示相似。通过顺序外切糖苷酶消化后进行FACE测定N - 连接糖链序列。结果表明是典型的N - 连接复合寡糖结构。含氨培养物中的聚糖显示出相同的序列模式。总之,我们表明培养基中的氨影响EPO糖基化,表现为四天线和四唾液酸化寡糖结构的减少。然而,培养物中氨的存在并未改变寡糖序列。