Scanlan Christopher N, Pantophlet Ralph, Wormald Mark R, Ollmann Saphire Erica, Stanfield Robyn, Wilson Ian A, Katinger Hermann, Dwek Raymond A, Rudd Pauline M, Burton Dennis R
The Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
J Virol. 2002 Jul;76(14):7306-21. doi: 10.1128/jvi.76.14.7306-7321.2002.
2G12 is a broadly neutralizing human monoclonal antibody against human immunodeficiency virus type-1 (HIV-1) that has previously been shown to bind to a carbohydrate-dependent epitope on gp120. Here, site-directed mutagenesis and carbohydrate analysis were used to define further the 2G12 epitope. Extensive alanine scanning mutagenesis showed that elimination of the N-linked carbohydrate attachment sequences associated with residues N295, N332, N339, N386, and N392 by N-->A substitution produced significant decreases in 2G12 binding affinity to gp120(JR-CSF). Further mutagenesis suggested that the glycans at N339 and N386 were not critical for 2G12 binding to gp120(JR-CSF). Comparison of the sequences of isolates neutralized by 2G12 was also consistent with a lesser role for glycans attached at these positions. The mutagenesis studies provided no convincing evidence for the involvement of gp120 amino acid side chains in 2G12 binding. Antibody binding was inhibited when gp120 was treated with Aspergillus saitoi mannosidase, Jack Bean mannosidase, or endoglycosidase H, indicating that Man(alpha)1-->2Man-linked sugars of oligomannose glycans on gp120 are required for 2G12 binding. Consistent with this finding, the binding of 2G12 to gp120 could be inhibited by monomeric mannose but not by galactose, glucose, or N-acetylglucosamine. The inability of 2G12 to bind to gp120 produced in the presence of the glucose analogue N-butyl-deoxynojirimycin similarly implicated Man(alpha)1-->2Man-linked sugars in 2G12 binding. Competition experiments between 2G12 and the lectin cyanovirin for binding to gp120 showed that 2G12 only interacts with a subset of available Man(alpha)1-->2Man-linked sugars. Consideration of all the data, together with inspection of a molecular model of gp120, suggests that the most likely epitope for 2G12 is formed from mannose residues contributed by the glycans attached to N295 and N332, with the other glycans playing an indirect role in maintaining epitope conformation.
2G12是一种广泛中和的抗人类免疫缺陷病毒1型(HIV-1)的人源单克隆抗体,此前已证明它能结合gp120上一个依赖碳水化合物的表位。在此,利用定点诱变和碳水化合物分析进一步确定2G12表位。广泛的丙氨酸扫描诱变表明,通过N→A替换消除与N295、N332、N339、N386和N392残基相关的N-连接碳水化合物连接序列,会使2G12与gp120(JR-CSF)的结合亲和力显著降低。进一步的诱变表明,N339和N386处的聚糖对2G12与gp120(JR-CSF)的结合并不关键。对被2G12中和的分离株序列的比较也与这些位置连接的聚糖作用较小一致。诱变研究没有提供令人信服的证据表明gp120氨基酸侧链参与2G12结合。当用斋藤曲霉甘露糖苷酶、刀豆甘露糖苷酶或内切糖苷酶H处理gp120时,抗体结合受到抑制,这表明gp120上寡甘露糖聚糖的Man(α)1→2Man连接糖是2G12结合所必需的。与此发现一致,2G12与gp120的结合可被单体甘露糖抑制,但不能被半乳糖、葡萄糖或N-乙酰葡糖胺抑制。在葡萄糖类似物N-丁基-脱氧野尻霉素存在下产生的2G12无法与gp120结合,同样表明Man(α)1→2Man连接糖参与2G12结合。2G12与凝集素氰病毒素竞争结合gp120的实验表明,2G12仅与一部分可用的Man(α)1→2Man连接糖相互作用。综合所有数据,并检查gp120的分子模型,表明2G12最可能的表位由连接到N295和N332的聚糖贡献的甘露糖残基形成,其他聚糖在维持表位构象中起间接作用。