Nakane P K, Pierce G B
J Cell Biol. 1967 May;33(2):307-18. doi: 10.1083/jcb.33.2.307.
Enzymes, either acid phosphatase or horseradish peroxidase, were conjugated to antibodies with bifunctional reagents. The conjugates, enzymatically and immunologically active, were employed in the immunohistochemical localization of tissue antigens utilizing the reaction product of the enzymatic reaction as the marker. Tissues reacted with acid phosphatase-labeled antibodies directed against basement membrane were stained for the enzyme with Gomori's method, and those reacted with peroxidase-labeled antibody were stained with Karnovsky's method. The reaction products of the enzymes localized in the basement membrane. Unlike the preparations of the fluorescent antibody technique, enzyme-labeled antibody preparations were permanent, could be observed with an ordinary microscope, and could be examined with the electron microscope. In the latter, specific localization of antibody occurred in the basement membrane and in the endoplasmic reticulum of cells known to synthesize basement membrane antigens. The method is sensitive because of the amplifying effect of the enzymatic activity. The ultrastructural preservation and localization were better with acid phosphatase-labeled antibody than with peroxidase-labeled antibody, but acid phosphatase conjugated antibody was unstable and difficult to prepare. Peroxidase-antibody conjugates were stable and could be stored for several months at 4 degrees C, or indefiniely in a frozen state.
用双功能试剂将酸性磷酸酶或辣根过氧化物酶等酶与抗体结合。这些具有酶活性和免疫活性的结合物,利用酶促反应的产物作为标记,用于组织抗原的免疫组织化学定位。与抗基底膜的酸性磷酸酶标记抗体反应的组织,用Gomori法对该酶进行染色,与过氧化物酶标记抗体反应的组织则用Karnovsky法染色。酶的反应产物定位于基底膜。与荧光抗体技术的制剂不同,酶标记抗体制剂是永久性的,可用普通显微镜观察,也可用电子显微镜检查。在电子显微镜下,抗体的特异性定位出现在基底膜和已知合成基底膜抗原的细胞内质网中。由于酶活性的放大作用,该方法很灵敏。酸性磷酸酶标记抗体的超微结构保存和定位比过氧化物酶标记抗体更好,但酸性磷酸酶结合抗体不稳定且难以制备。过氧化物酶-抗体制剂稳定,可在4℃下保存数月,或在冷冻状态下无限期保存。