Huang Jin, Dong Xiaonan, Liu Zuqiang, Qin Li, Chen Ying-Hua
Laboratory of Immunology, Department of Biology, Research Centre for Medical Science, Tsinghua University, Protein Science Laboratory of the Ministry of Education, Beijing 100084, People's Republic of China.
Immunol Lett. 2002 Dec 3;84(3):205-9. doi: 10.1016/s0165-2478(02)00174-8.
Diverse variation of HIV-1 is a grave challenge for prevention of viral infection and immunotherapy. Monoclonal antibody (mAb) 2F5 recognizing an epitope ELDKWA (aa669-674) on HIV-1 envelope protein gp41 showed broad neutralizing activity against a lot of HIV-1 strains including primary isolates. However, viral mutation from ELDKWA to ELDEWA resulted in viral evasion from neutralization by mAb 2F5. Using ELDEWA-epitope-peptide (C-GFLDEWAGELDEWA) conjugated with carrier protein keyhole limpet hemocyanin (KLH), a mAb 14D9 (IgGl) was prepared and identified as the mAb with predefined ELDEWA-epitope specificity. The mAb 14D9 recognized the ELDEWA epitope, but not other three epitopes (ELDKWA, ELNKWA and ELEKWA). In comparison, mAb 2F5 could recognize only ELDKWA, but not three neutralization-resistant epitopes (ELDEWA, ELNKWA and ELEKWA). Interestingly, we searched several authoritative HIV sequence databases (http://hiv-web.lanl.gov) and found out that nearly all the viral isolates bearing the ELDEWA epitope belong to the O clade, the only exceptional viral isolate bearing the epitope ELDEWA has been demonstrated to be an intergroup M/O recombinant, which suggests that the ELDEWA-epitope on gp41 represents a specific epitope-marker of HIV-1 O clade. To confirm whether the mAb 14D9 recognizes gp41 of HIV-1 O clade, the rsgp41(IIIB), bearing ELDKWA-epitope was site-directed-mutated to the rsgp41 bearing ELDEWA-epitope. The mAb 14D9 could bind to rsgp41 bearing ELDEWA-epitope in immunoblotting analysis, did not bind to rsgp41 bearing ELDKWA-epitope. These experimental results suggest that the mAb 14D9 with predefined ELDEWA-epitope specificity may be applied to HIV-1 O clade identification.
HIV-1的多样变异是预防病毒感染和免疫治疗的严峻挑战。识别HIV-1包膜蛋白gp41上一个表位ELDKWA(氨基酸669 - 674)的单克隆抗体(mAb)2F5对包括原代分离株在内的许多HIV-1毒株表现出广泛的中和活性。然而,从ELDKWA到ELDEWA的病毒突变导致病毒逃避mAb 2F5的中和作用。使用与载体蛋白钥孔血蓝蛋白(KLH)偶联的ELDEWA表位肽(C-GFLDEWAGELDEWA),制备了单克隆抗体14D9(IgG1),并鉴定为具有预定义ELDEWA表位特异性的单克隆抗体。单克隆抗体14D9识别ELDEWA表位,但不识别其他三个表位(ELDKWA、ELNKWA和ELEKWA)。相比之下,单克隆抗体2F5只能识别ELDKWA,而不能识别三个中和抗性表位(ELDEWA、ELNKWA和ELEKWA)。有趣的是,我们搜索了几个权威的HIV序列数据库(http://hiv-web.lanl.gov),发现几乎所有携带ELDEWA表位的病毒分离株都属于O分支,唯一携带ELDEWA表位的例外病毒分离株已被证明是M/O组间重组体,这表明gp41上的ELDEWA表位代表HIV-1 O分支的一个特异性表位标记。为了确认单克隆抗体14D9是否识别HIV-1 O分支的gp41,将携带ELDKWA表位的rsgp41(IIIB)进行定点突变,得到携带ELDEWA表位的rsgp41。在免疫印迹分析中,单克隆抗体14D9能与携带ELDEWA表位的rsgp41结合,而不与携带ELDKWA表位的rsgp41结合。这些实验结果表明,具有预定义ELDEWA表位特异性的单克隆抗体14D9可用于HIV-1 O分支的鉴定。