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识别7-(2-羟乙基)鸟嘌呤和咪唑环开环的7-(2-羟乙基)鸟嘌呤的单克隆抗体的研制。

Development of monoclonal antibodies recognizing 7-(2-hydroxyethyl)guanine and imidazole ring-opened 7-(2-hydroxyethyl)guanine.

作者信息

Young T L, Habraken Y, Ludlum D B, Santella R M

机构信息

Cancer Center, School of Public Health, Columbia University, New York, NY 10032.

出版信息

Carcinogenesis. 1990 Oct;11(10):1685-9. doi: 10.1093/carcin/11.10.1685.

Abstract

7-(2-Hydroxyethyl)guanine (7HEG) is of biological interest because it is formed in vivo by reaction of DNA with ethylene oxide (EO). Furthermore, the major DNA adduct of vinyl chloride, 7-(2-oxyethyl)guanine, can be converted to this adduct by reduction. Two monoclonal antibodies (9E2, 4A5) recognizing 7HEG have been developed from BALB/c mice immunized with the adduct coupled to keyhole limpet hemocyanin. In addition, another antibody (8E10) was developed against the imidazole ring-opened form of the adduct (ro-7HEG). ELISAs were used to determine the sensitivity and specificity of these antibodies. With antibody 9E2, 50% inhibition of antibody binding in the competitive ELISA was at 54 pmol of the modified base 7HEG/well and 67 pmol 7HEGR/well, while with antibody 4A5, the values were 3.6 pmol 7HEG/well and 6.7 pmol 7HEGR/well. Antibody 8E10 gave 50% inhibition at 48 pmol ro-7HEGR/well. Neither antibody 9E2 nor 8E10 cross-reacted with unmodified DNA or with the normal nucleosides at the highest concentration tested. However, antibody 4A5 had a low affinity for deoxyguanosine (50% inhibition at 31,000 pmol). Sensitivity of adduct measurement can be increased 3- to 10-fold using an ELISA with fluorescence endpoint detection. These antibodies have been used to determine the level of adducts in DNA modified in vitro with [3H]- or [14C]EO. Because of the cross-reactivity of the most sensitive antibody, 4A5, with deoxyguanosine, a combined HPLC/immunoassay method was developed to quantitate 7HEG in DNA. The limit of sensitivity of this method is dependent upon the amount of DNA available for analysis. Using 30 fmol as the lowest detectable amount (20% inhibition) in the fluorescent ELISA with antibody 4A5 and 100 micrograms of DNA assayed per well, adduct levels of 1/10(7) nucleotide can be determined. This method was applied to DNA adduct detection in EO-treated myeloma cells and whole blood. Antibody 8E10 was also used in immunohistochemical studies to visualize ring-opened adducts in cells treated with EO followed by high pH. These antibodies will be used for the detection and quantitation of adducts in human samples.

摘要

7-(2-羟乙基)鸟嘌呤(7HEG)具有生物学意义,因为它是DNA与环氧乙烷(EO)在体内反应形成的。此外,氯乙烯的主要DNA加合物7-(2-氧乙基)鸟嘌呤可通过还原转化为该加合物。用与钥孔血蓝蛋白偶联的加合物免疫BALB/c小鼠,已开发出两种识别7HEG的单克隆抗体(9E2、4A5)。此外,还开发了另一种针对加合物咪唑环开环形式(ro-7HEG)的抗体(8E10)。采用酶联免疫吸附测定(ELISA)来确定这些抗体的敏感性和特异性。对于抗体9E2,竞争性ELISA中抗体结合的50%抑制浓度在修饰碱基7HEG为54 pmol/孔和7HEGR为67 pmol/孔时,而对于抗体4A5,该值分别为3.6 pmol 7HEG/孔和6.7 pmol 7HEGR/孔。抗体8E10在ro-7HEGR为48 pmol/孔时产生50%抑制。在测试的最高浓度下,抗体9E2和8E10均未与未修饰的DNA或正常核苷发生交叉反应。然而,抗体4A5对脱氧鸟苷的亲和力较低(在31,000 pmol时50%抑制)。使用具有荧光终点检测的ELISA,加合物测量的灵敏度可提高3至10倍。这些抗体已用于测定用[3H]-或[14C]EO体外修饰的DNA中的加合物水平。由于最敏感的抗体4A5与脱氧鸟苷有交叉反应,因此开发了一种高效液相色谱/免疫测定联合方法来定量DNA中的7HEG。该方法的灵敏度极限取决于可用于分析的DNA量。在使用抗体4A5的荧光ELISA中,以30 fmol作为最低可检测量(20%抑制),每孔测定100微克DNA,可测定1/10(7)核苷酸的加合物水平。该方法应用于EO处理的骨髓瘤细胞和全血中的DNA加合物检测。抗体8E10还用于免疫组织化学研究,以观察经EO处理后再用高pH处理的细胞中的开环加合物。这些抗体将用于检测和定量人类样品中的加合物。

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