Zagury J F, Cantalloube H, Achour A, Cho Y Y, Fall L, Lachgar A, Chams V, Astgen A, Biou D, Picard O
Laboratoire de Physiopathologie Cellulaire, Université P & M Curie, Paris, France.
Biomed Pharmacother. 1993;47(8):331-5. doi: 10.1016/0753-3322(93)90082-v.
We have designed a computer strategy in order to detect systematically peptidic sites with the potential of interfering with the immune regulatory processes. Applying this software to HIV-1 proteins has led us to unravel a few peptidic sites which could either act directly or be the targets of an auto-immune reaction during HIV-1 infection. We previously reported that the SLWDQ pentapeptide identity with a critical site of CD4 could trigger in HIV-1 infected individuals both an humoral and a cellular autoimmune reaction. In this study, we focused on surprising similitudes unravelled by our software Automat, between HIV-1/2 and another immunoregulatory molecule, the Fas protein which is also called the apoptosis-mediating cell-surface antigen.
我们设计了一种计算机策略,以便系统地检测具有干扰免疫调节过程潜力的肽段位点。将该软件应用于HIV-1蛋白,使我们发现了一些肽段位点,它们可能在HIV-1感染期间直接发挥作用,或者成为自身免疫反应的靶点。我们之前报道过,与CD4关键位点相同的SLWDQ五肽序列,可在HIV-1感染个体中引发体液和细胞自身免疫反应。在本研究中,我们聚焦于我们的软件Automat所揭示的HIV-1/2与另一种免疫调节分子Fas蛋白(也称为凋亡介导细胞表面抗原)之间惊人的相似性。