Erickson J S, Dalton B J, Paucker K
Arch Virol. 1980;63(3-4):253-61. doi: 10.1007/BF01315031.
Human interferons of lymphoid and nonlymphoid origins were segregated into several fractions by virtue of their elution properties from Blue Sepharose. According to desorption of the main portion of antiviral activity, three major classes could be discerned: 1. Leukocyte interferons eluting predominantly in 0.5 M NaCl buffer, 2. Lymphoblastoid interferons eluting mostly in 1 M NaCl buffer, and 3. Cell culture-derived fibroblast and bladder carcinoma interferons requiring ethylene glycol in addition to 1 M NaCl for elution. Desorption behavior from Blue Sepharose did not necessarily correlate with the presence of specific antigenic markers and no consistent segregation of Le and F antigens in individual fractions was observed. All fractions exhibited comparable activity in heterologous sheep and homologous human cells. Therefore, no distinctive biological features could be associated with multiple interferon species isolated by Blue Sepharose chromatography.
源自淋巴和非淋巴的人干扰素根据其从蓝色琼脂糖凝胶上的洗脱特性被分离成几个组分。根据抗病毒活性主要部分的解吸情况,可以区分出三大类:1. 主要在0.5M NaCl缓冲液中洗脱的白细胞干扰素;2. 大多在1M NaCl缓冲液中洗脱的淋巴母细胞干扰素;3. 细胞培养来源的成纤维细胞和膀胱癌干扰素,除1M NaCl外还需要乙二醇才能洗脱。从蓝色琼脂糖凝胶上的解吸行为不一定与特定抗原标记的存在相关,并且在各个组分中未观察到Le和F抗原的一致分离。所有组分在异源绵羊和同源人类细胞中均表现出相当的活性。因此,通过蓝色琼脂糖凝胶色谱法分离出的多种干扰素种类没有明显的生物学特征。