Labrousse H, Adib-Conquy M, Avrameas S
Unité d'Immunocytochimie, CNRS URA 1961, Institut Pasteur, Paris.
Res Immunol. 1997 May;148(4):267-76. doi: 10.1016/s0923-2494(97)80868-1.
In this study, the reactivities of two groups of murine monoclonal antibodies (mAbs) of the IgG isotype were compared by ELISA at various temperatures (Ts) (range: 4-56 degrees C). The first group was constituted of 4 polyreactive mAbs that reacted with various antigens (Ags), such as actin, myosin and tubulin. The second contained 3 commercially available monoreactive mAbs specific to actin, myosin or tubulin. The binding of the monospecific mAbs to their Ags was modified only slightly at the other Ts compared with binding at 37 degrees C. In contrast, the activities of the polyreactive IgGs were considerably modified depending upon the T during incubation on Ag. In a second series of experiments, the effects of the T of the washes and conjugate incubation on the mAb/Ag interaction were evaluated. In these experiments, all steps and incubations were carried out at 37 or 4 degrees C. The values were then compared to those obtained when the washes and conjugate incubation were performed at room temperature. These two protocols generated very little difference in terms of monospecific mAbs. For polyreactive IgG, the values were generally lower when the incubations were carried out at 4 degrees C. However, on the whole, the effect of the T of the washes and conjugate incubation was negligible when the mAb/Ag complex had already formed on the polystyrene plate. Furthermore, at 4 degrees C, 2 of the polyreactive mAbs behaved like monospecific antibodies, while the other 2 remained polyspecific. It can be concluded from these experiments that the reactivities of polyreactive mAbs are more T-sensitive than those of monoreactive mAbs. This seems to indicate that they may possess a more plastic structure and thus may more easily undergo deformation when subjected to non-physiological conditions. In addition, the fact that the polyreactive mAbs showed the same variations for the 3 Ag tested suggests that the same paratope could be involved in all reactions.
在本研究中,通过酶联免疫吸附测定(ELISA)在不同温度(T)(范围:4 - 56摄氏度)下比较了两组IgG同种型的鼠单克隆抗体(mAb)的反应活性。第一组由4种多反应性mAb组成,它们与多种抗原(Ag)反应,如肌动蛋白、肌球蛋白和微管蛋白。第二组包含3种市售的分别对肌动蛋白、肌球蛋白或微管蛋白具有特异性的单反应性mAb。与在37摄氏度时的结合相比,单特异性mAb与它们的Ag的结合在其他温度下仅有轻微改变。相反,多反应性IgG的活性根据在抗原上孵育时的温度而有相当大的改变。在第二系列实验中,评估了洗涤和共轭孵育温度对mAb/Ag相互作用(反应)的影响。在这些实验中,所有步骤和孵育均在37或4摄氏度下进行。然后将这些值与在室温下进行洗涤和共轭孵育时获得的值进行比较。对于单特异性mAb,这两种方案产生的差异非常小。对于多反应性IgG,当在4摄氏度下进行孵育时,其值通常较低。然而,总体而言,当mAb/Ag复合物已经在聚苯乙烯板上形成时,洗涤和共轭孵育温度的影响可以忽略不计。此外,在4摄氏度时,2种多反应性mAb表现得像单特异性抗体,而另外2种仍保持多特异性。从这些实验可以得出结论,多反应性mAb的反应活性比单反应性mAb对温度更敏感。这似乎表明它们可能具有更具可塑性的结构,因此在非生理条件下可能更容易发生变形。此外,多反应性mAb对所测试的3种抗原表现出相同变化这一事实表明,所有反应中可能涉及相同的互补决定区。