Hertzog P J, Smith J R, Garner R C
Carcinogenesis. 1982;3(7):825-8. doi: 10.1093/carcin/3.7.825.
Monoclonal antibodiess were produced following immunisation of mice with guanine imidazole ring-opened aflatoxin B1 DNA (iro AFB1 DNA), coupled electrostatically to methylated keyhole limpet haemocyanin. Three monoclonal hybridoma lines producing antibodies specific for iro AFB1 DNA were grown as ascites tumours and suitable dilutions of the ascitic fluid (1:8000-1:50,000) used in a competitive enzyme linked immunosorbent assay (ELISA) to measure reactivity of the antibodies to a variety of aflatoxin and nucleic acid-related compounds. These antibodies recognise AFB1 bound to DNA at levels 10(4)-10(5) times lower concentration than unmodified calf thymus DNA or 8,9-dihydro-8,9-dihydroxy-aflatoxin B1: and show 2-5 times the affinity to iro AFB1 DNA compared to AFB1 DNA. The concentration of AFB1 in iro AFB1 DNA producing 50% inhibition in a competitive ELISA was 1.8 x 10(-7) molar. Using the most sensitive hybridoma line, levels of 1 adduct in 300,000 nucleotides would be detectable, which is the level of binding found in the rat and the hamster in vivo. These monoclonal antibodie should therefore prove useful in detecting these lesions in animal and human tissue samples exposed to aflatoxins.
用静电偶联到甲基化钥孔血蓝蛋白上的鸟嘌呤咪唑环开环黄曲霉毒素B1 DNA(iro AFB1 DNA)免疫小鼠后产生了单克隆抗体。三种产生对iro AFB1 DNA具有特异性抗体的单克隆杂交瘤细胞系作为腹水肿瘤生长,并将腹水的合适稀释液(1:8000 - 1:50000)用于竞争性酶联免疫吸附测定(ELISA),以测量抗体对多种黄曲霉毒素和核酸相关化合物的反应性。这些抗体识别与DNA结合的AFB1时,其浓度比未修饰的小牛胸腺DNA或8,9 - 二氢 - 8,9 - 二羟基黄曲霉毒素B1低10⁴ - 10⁵倍:并且与AFB1 DNA相比,对iro AFB1 DNA的亲和力高2 - 5倍。在竞争性ELISA中产生50%抑制的iro AFB1 DNA中AFB1的浓度为1.8×10⁻⁷摩尔。使用最敏感的杂交瘤细胞系,在300,000个核苷酸中可检测到1个加合物的水平,这是在大鼠和仓鼠体内发现的结合水平。因此,这些单克隆抗体应可用于检测暴露于黄曲霉毒素的动物和人类组织样本中的这些损伤。