The Protein Crystallography Unit, ARC Centre of Excellence in Structural and Functional Microbial Genomics, Department of Biochemistry and Molecular Biology, School of Biomedical Sciences, Monash University, Clayton, Victoria 3800, Australia.
Immunity. 2011 Mar 25;34(3):327-39. doi: 10.1016/j.immuni.2011.02.001. Epub 2011 Mar 3.
Natural killer T (NKT) cells respond to a variety of CD1d-restricted antigens (Ags), although the basis for Ag discrimination by the NKT cell receptor (TCR) is unclear. Here we have described NKT TCR fine specificity against several closely related Ags, termed altered glycolipid ligands (AGLs), which differentially stimulate NKT cells. The structures of five ternary complexes all revealed similar docking. Acyl chain modifications did not affect the interaction, but reduced NKT cell proliferation, indicating an affect on Ag processing or presentation. Conversely, truncation of the phytosphingosine chain caused an induced fit mode of TCR binding that affected TCR affinity. Modifications in the glycosyl head group had a direct impact on the TCR interaction and associated cellular response, with ligand potency reflecting the t(1/2) life of the interaction. Accordingly, we have provided a molecular basis for understanding how modifications in AGLs can result in striking alterations in the cellular response of NKT cells.
自然杀伤 T(NKT)细胞对多种 CD1d 限制的抗原(Ag)作出反应,尽管 NKT 细胞受体(TCR)对抗原的识别基础尚不清楚。在这里,我们描述了针对几种密切相关的抗原,称为改变的糖脂配体(AGL)的 NKT TCR 精细特异性,这些抗原可不同程度地刺激 NKT 细胞。五种三元复合物的结构均显示出相似的对接。酰基链修饰不影响相互作用,但会降低 NKT 细胞的增殖,表明其对 Ag 加工或呈递有影响。相反,植烷醇链的截断导致 TCR 结合的诱导契合模式,从而影响 TCR 亲和力。糖基头部基团的修饰对 TCR 相互作用和相关的细胞反应有直接影响,配体效力反映了相互作用的 t(1/2)寿命。因此,我们为理解 AGL 中的修饰如何导致 NKT 细胞的细胞反应发生显著改变提供了分子基础。