Van Damme J, Billiau A, De Ley M, De Somer P
J Gen Virol. 1983 Aug;64 (Pt 8):1819-22. doi: 10.1099/0022-1317-64-8-1819.
Human peripheral blood leukocytes were treated with concanavalin A (Con A) to produce interferon gamma (HuIFN-gamma). On gel filtration this interferon eluted as a protein with a molecular weight of 45000. In addition to this, the culture supernatant contained an interferon-like protein of apparent molecular weight 22000 (22K factor). The antiviral activity of this protein was neutralizable by a highly specific antibody to HuIFN-beta. Yet, the 22K factor differed from classical HuIFN-beta in several characteristics: lack of activity on certain homologous and heterologous cells which are sensitive to HuIFN-beta; lack of affinity for zinc-chelate and Con A-Sepharose columns; failure to bind to an anti-HuIFN-beta antibody column. Moreover, a specific antiserum raised against the 22K factor did not neutralize HuIFN-beta. Two alternative explanations of these findings are proposed: (i) the 22K factor is an interferon whose molecular structure resembles that of the known HuIFN-beta but it is not identical to it, or (ii) the 22K factor is not an interferon but a protein that can induce the production of HuIFN-beta in certain lines of fibroblastoid cells.
用人外周血白细胞与伴刀豆球蛋白A(Con A)处理以产生γ干扰素(HuIFN-γ)。经凝胶过滤,这种干扰素作为一种分子量为45000的蛋白质被洗脱出来。除此之外,培养上清液中还含有一种表观分子量为22000的类干扰素蛋白(22K因子)。这种蛋白质的抗病毒活性可被针对HuIFN-β的高度特异性抗体中和。然而,22K因子在几个特征上与经典的HuIFN-β不同:对某些对HuIFN-β敏感的同源和异源细胞缺乏活性;对锌螯合柱和Con A-琼脂糖柱缺乏亲和力;不能与抗HuIFN-β抗体柱结合。此外,针对22K因子产生的特异性抗血清不能中和HuIFN-β。针对这些发现提出了两种不同的解释:(i)22K因子是一种干扰素,其分子结构与已知的HuIFN-β相似但并不相同,或者(ii)22K因子不是一种干扰素,而是一种能在某些成纤维样细胞系中诱导HuIFN-β产生的蛋白质。