Tayapiwatana C, Poonpipat P
Department of Clinical Immunology, Faculty of Associated Medical Sciences, Chiang Mai University, Thailand.
Asian Pac J Allergy Immunol. 1998 Jun-Sep;16(2-3):127-35.
Human chorionic gonadotropin (hCG) hormone is required for maintenance of early pregnancy and is a potential marker in the diagnosis and prognosis of both pregnancy and trophoblastic diseases. Murine hybridomas were generated against purified hCG. Seven hybrid clones secreting antibodies against hCG molecule with IgG1/kappa subclass were established. The indirect ELISA result demonstrated that six MAbs (BEL-1 to BEL-6) recognized hCG in both holo and free beta subunit form with negligible cross-reactivity against a closely related hormone, human luteinizing hormone (hLH). In this fusion, only one MAb (ALC-1) showed a cross-reaction with hLH, which designated an alpha subunit specific. The outcome of Western blot ascertained that ALC-1 recognized the conformational epitope on alpha subunit of hCG at Mr 23 kDa band in nonreducing condition (NR). In contrast, epitopes belonging to all MAbs recognized beta subunit of hCG were in linear peptide structure at Mr 34 kDa band (NR) and Mr 26 kDa band (R). These six MAbs were further characterized by using two beta subunit carboxy-terminal synthetic peptides (beta109-119 and beta109-145). Three of them (BEL-1, BEL-3, and BEL-4) recognized only epitope harboring in beta109-145 fragment, the others recognized both types of the synthetic peptide. In order to select the most suitable MAbs specific to beta subunit of hCG for exploiting with ALC-1 in the sandwich-type immunometric assay, competitive ELISA was employed. Six individual MAbs specific to beta subunit of hCG were used to compete with biotinylated ALC-1 to evaluate the proximity of their epitopes on the holo form of hCG molecule. Of all six MAbs, BEL-5 depicted the lowest percent inhibition result, which indicated the bottom-most steric hindrance effect. Consequently, MAb BEL-5 will be the most appropriate antibody to utilize in concert with ALC-1 in place of devising a sandwich-type immunometric assay for measuring holo-hCG level.
人绒毛膜促性腺激素(hCG)对于维持早期妊娠至关重要,并且是妊娠和滋养细胞疾病诊断及预后的潜在标志物。制备了针对纯化hCG的小鼠杂交瘤。建立了七个分泌抗hCG分子抗体的杂交克隆,其亚类为IgG1/κ。间接ELISA结果表明,六种单克隆抗体(BEL-1至BEL-6)能识别完整形式和游离β亚基形式的hCG,与密切相关的激素人促黄体生成素(hLH)的交叉反应可忽略不计。在此次融合中,只有一种单克隆抗体(ALC-1)与hLH发生交叉反应,表明其具有α亚基特异性。Western印迹结果确定,ALC-1在非还原条件(NR)下识别hCGα亚基上Mr 23 kDa条带处的构象表位。相比之下,所有识别hCGβ亚基的单克隆抗体的表位在Mr 34 kDa条带(NR)和Mr 26 kDa条带(R)处呈线性肽结构。使用两种β亚基羧基末端合成肽(β109-119和β109-145)对这六种单克隆抗体进行了进一步表征。其中三种(BEL-1、BEL-3和BEL-4)仅识别β109-145片段中的表位,其他几种则识别两种合成肽。为了选择最适合与ALC-1一起用于夹心型免疫测定的hCGβ亚基特异性单克隆抗体,采用了竞争ELISA法。使用六种hCGβ亚基特异性单克隆抗体与生物素化的ALC-1竞争,以评估它们在hCG分子完整形式上的表位接近程度。在所有六种单克隆抗体中,BEL-5的抑制百分比结果最低,这表明其空间位阻效应最小。因此,单克隆抗体BEL-5将是与ALC-1协同使用以设计用于测量完整hCG水平的夹心型免疫测定的最合适抗体。