Gerritse K, Fasbender M, Boersma W, Claassen E
Department of Immunology, Medical Biological Laboratory TNO, Rijswijk, The Netherlands.
J Histochem Cytochem. 1991 Jul;39(7):987-92. doi: 10.1177/39.7.1865115.
We report here a new method to produce synthetic peptide/alkaline phosphatase (AP) conjugates in the presence of urea. The method allows the use of peptides that are not soluble to a sufficient degree in aqueous buffers. The presence of 8 M urea during the construction of the synthetic peptide/AP conjugates does not influence enzyme activity nor the affinity of the anti-peptide antibodies for the conjugated peptide. We demonstrate that these synthetic peptide/AP conjugates can be used for detection of specific antipeptide antibody-forming cells (AFC) in vivo. This method for constructing enzyme conjugates with insoluble proteins or peptides suggest not only new possibilities for detection of specific AFC in vivo but also for applications in receptor-ligand studies, ELISA (enzyme-linked immunosorbent assay), and spot ELISA for detection of antibody-secreting cells in vitro.
我们在此报告一种在尿素存在下制备合成肽/碱性磷酸酶(AP)偶联物的新方法。该方法允许使用在水性缓冲液中溶解度不足的肽。在合成肽/AP偶联物构建过程中8M尿素的存在既不影响酶活性,也不影响抗肽抗体对偶联肽的亲和力。我们证明这些合成肽/AP偶联物可用于体内检测特异性抗肽抗体形成细胞(AFC)。这种用于构建与不溶性蛋白质或肽的酶偶联物的方法不仅为体内检测特异性AFC提供了新的可能性,也为受体-配体研究、ELISA(酶联免疫吸附测定)以及用于体外检测抗体分泌细胞的斑点ELISA中的应用提供了新的可能性。