Theoretical Molecular Biophysics Group, Max Planck Institute of Biophysics, Max von Laue Strasse 3, 60438 Frankfurt am Main, Germany.
J Biol Chem. 2013 Jul 5;288(27):19528-36. doi: 10.1074/jbc.M113.470179. Epub 2013 May 15.
CD1 proteins mediate the presentation of endogenous and foreign lipids on the cell surface for recognition by T cell receptors. To sample a diverse antigen pool, CD1 proteins are repeatedly internalized and recycled, assisted, in some cases, by lipid transfer proteins such as saposins. The specificity of each CD1 isoform is, therefore, conferred in part by its intracellular pathway but also by distinct structural features of the antigen-binding domain. Crystal structures of CD1-lipid complexes reveal hydrophobic grooves and pockets within these binding domains that appear to be specialized for different lipids. However, the mechanism of lipid loading and release remains to be characterized. Here we gain insights into this mechanism through a meta-analysis of the five human CD1 isoforms, in the lipid-bound and lipid-free states, using all-atom molecular dynamics simulations. Strikingly, for isoforms CD1b through CD1e, our simulations show the near-complete collapse of the hydrophobic cavities in the absence of the antigen. This event results from the spontaneous closure of the binding domain entrance, flanked by two α-helices. Accordingly, we show that the anatomy of the binding cavities is restored if these α-helices are repositioned extrinsically, suggesting that helper proteins encountered during recycling facilitate lipid exchange allosterically. By contrast, we show that the binding cavity of CD1a is largely preserved in the unliganded state because of persistent electrostatic interactions that keep the portal α-helices at a constant separation. The robustness of this binding groove is consistent with the observation that lipid exchange in CD1a is not dependent on cellular internalization.
CD1 蛋白介导细胞表面内源性和外源性脂质的呈递,以供 T 细胞受体识别。为了对多样化的抗原库进行采样,CD1 蛋白会被反复内化和再循环,在某些情况下,还会得到脂质转移蛋白(如 saposin)的辅助。因此,每种 CD1 同工型的特异性部分由其细胞内途径决定,但也由抗原结合域的独特结构特征决定。CD1-脂质复合物的晶体结构揭示了这些结合域内的疏水性槽和口袋,这些槽和口袋似乎专门用于不同的脂质。然而,脂质加载和释放的机制仍有待阐明。在这里,我们通过对五种人类 CD1 同工型(在结合脂质和无脂质状态下)进行全原子分子动力学模拟的元分析,深入了解了这一机制。引人注目的是,对于 CD1b 至 CD1e 同工型,我们的模拟显示在没有抗原的情况下,疏水性腔几乎完全塌陷。这一事件是由于结合域入口两侧的两个α-螺旋自发关闭所致。因此,我们表明,如果重新定位这些α-螺旋,结合腔的解剖结构可以恢复,这表明在再循环过程中遇到的辅助蛋白通过变构作用促进脂质交换。相比之下,我们表明 CD1a 的结合腔在未配体状态下基本保持完整,这是由于持续的静电相互作用使门户α-螺旋保持恒定的分离。这种结合槽的稳健性与 CD1a 中脂质交换不依赖于细胞内化的观察结果一致。