Kufareva Irina, Gustavsson Martin, Zheng Yi, Stephens Bryan S, Handel Tracy M
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, California 92093; email:
Annu Rev Biophys. 2017 May 22;46:175-198. doi: 10.1146/annurev-biophys-051013-022942.
Chemokines and their cell surface G protein-coupled receptors are critical for cell migration, not only in many fundamental biological processes but also in inflammatory diseases and cancer. Recent X-ray structures of two chemokines complexed with full-length receptors provided unprecedented insight into the atomic details of chemokine recognition and receptor activation, and computational modeling informed by new experiments leverages these insights to gain understanding of many more receptor:chemokine pairs. In parallel, chemokine receptor structures with small molecules reveal the complicated and diverse structural foundations of small molecule antagonism and allostery, highlight the inherent physicochemical challenges of receptor:chemokine interfaces, and suggest novel epitopes that can be exploited to overcome these challenges. The structures and models promote unique understanding of chemokine receptor biology, including the interpretation of two decades of experimental studies, and will undoubtedly assist future drug discovery endeavors.
趋化因子及其细胞表面G蛋白偶联受体对于细胞迁移至关重要,不仅在许多基本生物学过程中如此,在炎症性疾病和癌症中也是如此。最近两种趋化因子与全长受体复合物的X射线结构,为趋化因子识别和受体激活的原子细节提供了前所未有的见解,而基于新实验的计算模型利用这些见解来了解更多的受体:趋化因子对。同时,含有小分子的趋化因子受体结构揭示了小分子拮抗作用和变构作用的复杂多样的结构基础,突出了受体:趋化因子界面固有的物理化学挑战,并提出了可用于克服这些挑战的新表位。这些结构和模型促进了对趋化因子受体生物学的独特理解,包括对二十年实验研究的解读,无疑将有助于未来的药物发现工作。