Steinaa L, Wulff A M, Saermark T
Department of Infectious Diseases, Hvidovre Hospital, Denmark.
Hybridoma. 1994 Oct;13(5):383-8. doi: 10.1089/hyb.1994.13.383.
Monoclonal antibodies against a synthetic peptide (aa 138-152) from HIV-1 Nef protein were produced and characterized. Three hybridoma lines producing monoclonal antibodies (MAbs) against the synthetic peptide were generated by fusion between P3-X63 Ag8.653 myeloma cells and BALB/c splenocytes from mice immunized with the synthetic peptide coupled to keyhole limpet hemocyanin (KLH). The hybridomas were screened and selected by ELISA with the peptide coupled to bovine serum albumin (BSA) immobilized to the polystyrene surface and specificity for the peptide was confirmed by competitive ELISA with the peptide free in solution. The reactions of the MAbs with a 5-aa motif (WCYKL) included in the sequence were examined with synthetic peptides and two of the MAbs reacted with the motif. The recognitions of recombinant full-length Nef protein were also tested. One MAb reacted with the protein in both ELISA and dot blot, and one only in dot blot, whereas the last MAb did not recognize the recombinant full-length Nef protein.
制备并鉴定了针对来自HIV-1 Nef蛋白的合成肽(氨基酸138 - 152)的单克隆抗体。通过将P3-X63 Ag8.653骨髓瘤细胞与用偶联有钥孔血蓝蛋白(KLH)的合成肽免疫的BALB/c小鼠脾细胞进行融合,产生了三个产生针对该合成肽的单克隆抗体(MAb)的杂交瘤细胞系。通过酶联免疫吸附测定(ELISA)筛选并选择杂交瘤,其中将偶联到牛血清白蛋白(BSA)上的肽固定在聚苯乙烯表面,并且通过与溶液中游离肽的竞争性ELISA确认对该肽的特异性。用合成肽检测了单克隆抗体与该序列中包含的5个氨基酸基序(WCYKL)的反应,其中两个单克隆抗体与该基序发生反应。还测试了单克隆抗体对重组全长Nef蛋白的识别。一种单克隆抗体在ELISA和斑点印迹中均与该蛋白反应,一种仅在斑点印迹中反应,而最后一种单克隆抗体不识别重组全长Nef蛋白。