K Nishikawa, R A Newman, L Murray, A R Khokhar, M G Rosenblum
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引用次数: 0
摘要
利用酶联免疫吸附试验(ELISA),利用反式r, r -1,2-二氨基环己烷(DACH)修饰的铂类似物(DACH- pt - so4)与DNA络合,制备了一种单克隆抗体1C1,能够结合游离药物DACH- pt - so4和药物-DNA复合物。使用竞争性ELISA,发现1C1可以识别不含dach的铂化合物,如顺式二氯二胺铂(II) (CDDP)。1C1与凹槽印迹的DACH- pt - so4处理的DNA有很强的结合,与CDDP-DNA复合物有中等程度的结合,但不能检测含有甲基双乙酰氨基反式r, r -1,2-二氨基环己烷铂(II) (MIDP)修饰的DNA。使用1C1抗体对cddp处理的BRO黑色素瘤细胞进行免疫细胞化学染色研究显示,与细胞核相比,胞浆的染色更优先。虽然染色程度与剂量有关,但观察到异质染色模式。CDDP处理的MDA886LN鳞状癌细胞的多细胞球体在生长的周围呈强烈的染色,而球体内的染色较弱但均匀。同步的BRO细胞对CDDP的细胞周期依赖性摄取可能部分解释了观察到的铂分布的异质性。
Detection of cellular platinum using the monoclonal antibody 1C1.
A monoclonal antibody, 1C1, developed using a trans-R,R-1,2-diamminocyclohexane (DACH) modified platinum analog (DACH-Pt-SO4) complexed with DNA was shown, using the enzyme-linked immunosorbent assay (ELISA), to have the ability to bind to both free drug DACH-Pt-SO4 and to the drug-DNA complex. Using competitive ELISA, 1C1 was found to recognize non-DACH-containing platinum compounds, such as cis-dichlorodiammine platinum (II) (CDDP). 1C1 exhibited strong binding to slot-blotted, DACH-Pt-SO4-treated DNA and moderate binding to the CDDP-DNA complex, but was unable to detect DACH containing methyliminodiacetato-trans-R,R-1,2-diamminocyclohexane platinum (II) (MIDP)-modified DNA. Immunocytochemical staining studies using 1C1 antibody on CDDP-treated BRO melanoma cells showed preferential staining of the cytosol compared with the nucleus. Although the extent of staining was dose dependent, a heterogeneous staining pattern was observed. Multicellular spheroids of MDA886LN squamous carcinoma cells treated with CDDP showed intense staining on the growing periphery compared with weak but homogeneous staining within the spheroid. Cell cycle-dependent uptake of CDDP in synchronized BRO cells may partly explain the observed heterogeneity of platinum distribution.