Pescovitz O H, Gelato M C, Bundy M, Loriaux D L, Merriam G R, Pescovitz M D
J Immunol Methods. 1986 Nov 20;94(1-2):257-62. doi: 10.1016/0022-1759(86)90240-1.
Two murine monoclonal antibodies (mAbs) specific for human growth hormone releasing hormone (GHRH-44-NH2) were produced from a fusion of spleen cells from a BALB/c mouse immunized with GHRH-conjugated BSA with SP 2/0 myeloma cells. The antibodies were of the IgG1 kappa, and IgG2b-kappa isotypes. The binding of both antibodies to GHRH-coated plates was inhibited by a 30-44 amino acid fragment but not by a 1-26 fragment. Thus, both antibodies are directed against the carboxy terminus of the peptide. Furthermore, both antibodies bind to the same epitope on the 30-44 amino acid portion since they cross-inhibit each other's binding to intact GHRH. Using these mAbs, a direct binding GHRH enzyme-linked immunosorbent assay (ELISA) was developed which had a least detectable dose of 30 pg. The availability of these antibodies and their use in ELISA methodology permits consistent and specific detection of GHRH in a non-isotope assay. They should prove of value in screening acromegalic patients for ectopic sources of GHRH secretion and in studies of ontogenic analysis of GHRH production.
用生长激素释放激素(GHRH)偶联的牛血清白蛋白免疫BALB/c小鼠,取其脾细胞与SP 2/0骨髓瘤细胞融合,制备出两种特异性针对人生长激素释放激素(GHRH-44-NH2)的小鼠单克隆抗体(mAb)。这些抗体属于IgG1 κ和IgG2b-κ同种型。两种抗体与包被有GHRH的平板的结合均被30 - 44个氨基酸的片段抑制,但不被1 - 26个氨基酸的片段抑制。因此,两种抗体均针对该肽的羧基末端。此外,两种抗体在30 - 44个氨基酸部分结合相同的表位,因为它们相互交叉抑制彼此与完整GHRH的结合。利用这些单克隆抗体,开发了一种直接结合的GHRH酶联免疫吸附测定法(ELISA),其最低可检测剂量为30 pg。这些抗体的可得性及其在ELISA方法中的应用使得在非同位素测定中能够一致且特异性地检测GHRH。它们在筛选肢端肥大症患者的GHRH分泌异位来源以及GHRH产生的个体发生分析研究中应具有价值。