Wang Denong, Tang Jin, Tang Jiulai, Wang Lai-Xi
Tumor Glycomics Laboratory, SRI International Biosciences Division, Menlo Park, CA 94025, USA.
Department of Pediatrics, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, China.
Molecules. 2015 Mar 12;20(3):4610-22. doi: 10.3390/molecules20034610.
Identifying molecular targets for eliciting broadly virus-neutralizing antibodies is one of the key steps toward development of vaccines against emerging viral pathogens. Owing to genomic and somatic diversities among viral species, identifying protein targets for broad-spectrum virus neutralization is highly challenging even for the same virus, such as HIV-1. However, viruses rely on host glycosylation machineries to synthesize and express glycans and, thereby, may display common carbohydrate moieties. Thus, exploring glycan-binding profiles of broad-spectrum virus-neutralizing agents may provide key information to uncover the carbohydrate-based virus-neutralizing epitopes. In this study, we characterized two broadly HIV-neutralizing agents, human monoclonal antibody 2G12 and Galanthus nivalis lectin (GNA), for their viral targeting activities. Although these agents were known to be specific for oligomannosyl antigens, they differ strikingly in virus-binding activities. The former is HIV-1 specific; the latter is broadly reactive and is able to neutralize viruses of distinct phylogenetic origins, such as HIV-1, severe acute respiratory syndrome coronavirus (SARS-CoV), and human cytomegalovirus (HCMV). In carbohydrate microarray analyses, we explored the molecular basis underlying the striking differences in the spectrum of anti-virus activities of the two probes. Unlike 2G12, which is strictly specific for the high-density Man9GlcNAc2Asn (Man9)-clusters, GNA recognizes a number of N-glycan cryptic sugar moieties. These include not only the known oligomannosyl antigens but also previously unrecognized tri-antennary or multi-valent GlcNAc-terminating N-glycan epitopes (Tri/m-Gn). These findings highlight the potential of N-glycan cryptic sugar moieties as conserved targets for broad-spectrum virus neutralization and suggest the GNA-model of glycan-binding warrants focused investigation.
识别能够引发广泛病毒中和抗体的分子靶点是开发针对新型病毒病原体疫苗的关键步骤之一。由于病毒物种之间存在基因组和体细胞多样性,即使对于同一病毒,如HIV-1,识别广谱病毒中和的蛋白质靶点也极具挑战性。然而,病毒依赖宿主糖基化机制来合成和表达聚糖,因此可能会呈现共同的碳水化合物部分。因此,探索广谱病毒中和剂的聚糖结合谱可能为揭示基于碳水化合物的病毒中和表位提供关键信息。在本研究中,我们对两种广泛中和HIV的试剂,即人单克隆抗体2G12和雪花莲凝集素(GNA)的病毒靶向活性进行了表征。尽管已知这些试剂对低聚甘露糖基抗原具有特异性,但它们在病毒结合活性方面存在显著差异。前者对HIV-1具有特异性;后者具有广泛的反应性,能够中和不同系统发育起源的病毒,如HIV-1、严重急性呼吸综合征冠状病毒(SARS-CoV)和人巨细胞病毒(HCMV)。在碳水化合物微阵列分析中,我们探究了这两种探针抗病毒活性谱显著差异背后的分子基础。与严格特异性识别高密度Man9GlcNAc2Asn(Man9)簇的2G12不同,GNA识别多种N-聚糖隐蔽糖部分。这些不仅包括已知的低聚甘露糖基抗原,还包括以前未识别的三触角或多价GlcNAc末端N-聚糖表位(Tri/m-Gn)。这些发现突出了N-聚糖隐蔽糖部分作为广谱病毒中和保守靶点的潜力,并表明聚糖结合的GNA模型值得重点研究。