Coimbra Chemistry Center-Institute of Molecular Sciences (CQC-IMS), Department of Chemistry, University of Coimbra, 3004-535 Coimbra, Portugal.
BSIM Therapeutics, Instituto Pedro Nunes, 3030-199 Coimbra, Portugal.
Int J Mol Sci. 2022 Feb 26;23(5):2599. doi: 10.3390/ijms23052599.
Interleukin-1 receptor type 1 (IL-1R1) is a key player in inflammation and immune responses. This receptor regulates IL-1 activity in two forms: as a membrane-bound form and as a soluble ectodomain. The details and differences between the conformational dynamics of the membrane-bound and the soluble IL-1R1 ectodomains (ECDs) remain largely elusive. Here, we study and compare the structural dynamics of the soluble and membrane-bound IL-1R1-ECDs using molecular dynamics (MD) simulations, focusing on the flexible interdomain linker of the ECD, as well as the spatial rearrangements between the Ig-like domains of the ECD. To explore the membrane-bound conformations, a full-length IL-1R1 structural model was developed and subjected to classical equilibrium MD. Comparative analysis of multiple MD trajectories of the soluble and the membrane-bound IL-1R1-ECDs reveals that (i) as somewhat expected, the extent of the visited "open-to-closed" transitional states differs significantly between the soluble and membrane-bound forms; (ii) the soluble form presents open-closed transitions, sampling a wider rotational motion between the Ig-like domains of the ECD, visiting closed and "twisted" conformations in higher extent, whereas the membrane-bound form is characterized by more conformationally restricted states; (iii) interestingly, the backbone dihedral angles of residues Glu202, Glu203 and Asn204, located in the flexible linker, display the highest variations during the transition between discrete conformational states detected in IL-1R1, thus appearing to work as the "central wheel of a clock's movement". The simulations and analyses presented in this contribution offer a deeper insight into the structure and dynamics of IL-1R1, which may be explored in a drug discovery setting.
白细胞介素-1 受体 1(IL-1R1)是炎症和免疫反应中的关键分子。该受体以两种形式调节 IL-1 的活性:作为膜结合形式和可溶性胞外结构域。膜结合和可溶性 IL-1R1 胞外结构域(ECD)的构象动力学的细节和差异在很大程度上仍不清楚。在这里,我们使用分子动力学(MD)模拟研究和比较可溶性和膜结合 IL-1R1-ECD 的结构动力学,重点关注 ECD 的柔性结构域间连接以及 ECD 的 Ig 样结构域之间的空间重排。为了探索膜结合构象,我们构建了全长 IL-1R1 结构模型并进行了经典平衡 MD。对可溶性和膜结合 IL-1R1-ECD 的多个 MD 轨迹进行比较分析表明:(i)正如预期的那样,可溶性和膜结合形式之间“开-闭”过渡状态的程度差异很大;(ii)可溶性形式呈现开-闭转变,ECD 的 Ig 样结构域之间的旋转运动范围更广,访问闭和“扭曲”构象的程度更高,而膜结合形式的构象受到更多的限制;(iii)有趣的是,位于柔性连接中的残基 Glu202、Glu203 和 Asn204 的骨架二面角在 IL-1R1 中检测到的离散构象状态之间的转变过程中显示出最高的变化,因此似乎作为“时钟运动的中央轮”发挥作用。本研究中的模拟和分析提供了对 IL-1R1 结构和动力学的更深入了解,这可能在药物发现中得到探索。