Ratcliffe W A, Bowden S J, Emly J, Hughes S, Ratcliffe J G
Wolfson Research Laboratories, Department of Clinical Chemistry, Queen Elizabeth Medical Centre, Birmingham, U.K.
J Immunol Methods. 1992 Jan 21;146(1):33-42. doi: 10.1016/0022-1759(92)90045-u.
The production and characterisation of monoclonal antibodies (MAb) to the mid-region sequence 37-67 of human parathyroid hormone-related protein (PTHRP) is described. In spite of the poor immunogenicity of this sub-fragment of PTHRP, a high percentage of specific hybrids were produced by boosting with conjugate and free peptide prior to cell fusion. Seven of the MAbs produced cross-reacted with PTHRP37-67, PTHRP1-86 and native forms of PTHRP. Inhibition studies with peptide sub-fragments of PTHRP37-67 indicated that the majority recognised the 45-59 region. In a RIA for PTHRP1-86, detection limits ranged from 0.17 to 0.9 ng PTHRP1-86/tube, and no cross-reaction was found with PTH1-84. Two MAbs 1D11 and 4B10 were shown to be of potential use in measuring PTHRP1-86 in a two-site immunoradiometric assay in combination with either a solid phase consisting of a MAb to PTHRP1-34, or iodinated affinity purified rabbit antibodies to PTHRP1-34. MAb 1D11 coupled to Sepharose was suitable for immunoextraction of PTHRP, and successfully localised PTHRP on immunoblots. Two additional MAbs were produced which recognised an epitope unique to PTHRP37-67 located in the 37-46 region of the peptide.
本文描述了针对人甲状旁腺激素相关蛋白(PTHRP)中间区域序列37 - 67的单克隆抗体(MAb)的制备及特性鉴定。尽管PTHRP的这个亚片段免疫原性较差,但在细胞融合前通过用偶联物和游离肽加强免疫,产生了高比例的特异性杂交瘤。所产生的七种单克隆抗体与PTHRP37 - 67、PTHRP1 - 86及PTHRP的天然形式发生交叉反应。用PTHRP37 - 67的肽亚片段进行的抑制研究表明,大多数抗体识别45 - 59区域。在PTHRP1 - 86的放射免疫分析(RIA)中,检测限为0.17至0.9 ng PTHRP1 - 86/管,且未发现与PTH1 - 84有交叉反应。已证明两种单克隆抗体1D11和4B10在与针对PTHRP1 - 34的单克隆抗体组成的固相或碘化亲和纯化的兔抗PTHRP1 - 34抗体结合的两点免疫放射分析中,可用于检测PTHRP1 - 86。偶联到琼脂糖凝胶上的单克隆抗体1D11适用于PTHRP的免疫提取,并成功地在免疫印迹上定位了PTHRP。还产生了另外两种单克隆抗体,它们识别位于肽的37 - 46区域的PTHRP37 - 67特有的一个表位。