互补性(分子生物学)
分子识别
氢键
选择性
结合位点
结合选择性
化学
密度泛函理论
疏水效应
组合化学
材料科学
化学物理
纳米技术
分子
计算化学
生物
生物化学
有机化学
遗传学
催化作用
作者
Yanfang Wang,Song-Meng Wang,Xiaobin Zhang,Hao Nian,Li‐Shuo Zheng,Xiaoping Wang,Georg Schreckenbach,Wei Jiang,Liu‐Pan Yang,Lili Wang
标识
DOI:10.1002/anie.202310115
摘要
Precise binding towards structurally similar substrates is a common feature of biomolecular recognition. However, achieving such selectivity-especially in distinguishing subtle differences in substrates-with synthetic hosts can be quite challenging. Herein, we report a novel design strategy involving the combination of different rigid skeletons to adjust the distance between recognition sites within the cavity, which allows for the highly selective recognition of hydrogen-bonding complementary substrates, such as 4-chromanone. X-ray single-crystal structures and density functional theory calculations confirmed that the distance of endo-functionalized groups within the rigid cavity is crucial for achieving high binding selectivity through hydrogen bonding. The thermodynamic data and molecular dynamics simulations revealed a significant influence of the hydrophobic cavity on the binding affinity. The new receptor possesses both high selectivity and high affinity, which provide valuable insights for the design of customized receptors.
科研通智能强力驱动
Strongly Powered by AbleSci AI