Morita T, Ikeda S, Minoura Y, Kojima M, Tada M
Biophysics Unit, Aichi Cancer Center Research Institute, Nagoya.
Jpn J Cancer Res. 1988 Feb;79(2):195-203. doi: 10.1111/j.1349-7006.1988.tb01577.x.
Antibodies against 4-nitroquinoline 1-oxide (4NQO) adducts were elicited in rabbits immunized with 4NQO-modified DNA complexed with methylated bovine serum albumin. In enzyme-linked immunosorbent assay (ELISA), the antibodies could recognize either denatured or native 4NQO-modified DNA, but not unmodified DNA, DNA modified with other carcinogens or free 4NQO derivative. Modification levels as low as 5 mumol of adduct per one mole DNA nucleotide (5 adducts/10(6) nucleotides) can be easily detected by the competitive ELISA. Indirect immunofluorescence staining by anti 4NQO-DNA antibody indicated that the antibodies bound specifically to the nuclei of normal human skin fibroblast cells treated with 4NQO. The intensity of fluorescence was proportional to the dose of 4NQO used to treat the cells, and the fluorescence-positive cells could be detected after treatment with 0.25 microM 4NQO (which resulted in the formation of 10(4) adducts per cell). Applying the competitive ELISA to the quantitation of DNA-adducts in rats treated with 4NQO, it was confirmed that the sensitivity of immunochemical assays was equivalent to that of isotopic assays. These methods should be helpful in studies on the formation of adducts and their removal in cells and tissues.
用与甲基化牛血清白蛋白复合的4-硝基喹啉1-氧化物(4NQO)修饰的DNA免疫兔子,可诱导产生针对4NQO加合物的抗体。在酶联免疫吸附测定(ELISA)中,这些抗体能够识别变性或天然的4NQO修饰的DNA,但不能识别未修饰的DNA、用其他致癌物修饰的DNA或游离的4NQO衍生物。通过竞争性ELISA可以轻松检测到低至每摩尔DNA核苷酸5微摩尔加合物(5个加合物/10⁶个核苷酸)的修饰水平。抗4NQO-DNA抗体的间接免疫荧光染色表明,这些抗体与用4NQO处理的正常人皮肤成纤维细胞的细胞核特异性结合。荧光强度与用于处理细胞的4NQO剂量成正比,在用0.25微摩尔4NQO处理后(导致每个细胞形成10⁴个加合物)可以检测到荧光阳性细胞。将竞争性ELISA应用于定量用4NQO处理的大鼠中的DNA加合物,证实免疫化学测定的灵敏度与同位素测定相当。这些方法应有助于研究加合物在细胞和组织中的形成及其去除。