Melis Claudio, Chau P-L, Price Kerry L, Lummis Sarah C R, Molteni Carla
Physics Department, King's College London, Strand, London WC2R 2LS, United Kingdom.
J Phys Chem B. 2006 Dec 28;110(51):26313-9. doi: 10.1021/jp063762a.
The 5-HT3 receptor is a typical ligand-gated ion channel of the Cys-loop superfamily, which is activated by binding of serotonin (5-HT). Models of the binding site of this protein reveal potential interactions between 5-HT and Tyr143, Tyr153, and Tyr234. Here we describe a series of ab initio calculations, based on density functional theory, to assess the effects of mutating these tyrosine residues on the binding of 5-HT. A series of mutations to these tyrosines, previously studied experimentally, were tested, and the binding energies compared with the available experimental data. Our results show that Tyr153 could form a hydrogen bond with the tertiary amine of 5-HT, and that mutation in this location revealed binding energies broadly in line with experimentally determined EC50s. Tyr143 could also form a hydrogen bond, but as EC50s do not relate to binding energies, it is unlikely that such a bond is formed here. Tyr234 is quite distinct in that it may interact with 5-HT via a mixed hydrogen bond/cation-pi interaction.
5-羟色胺3(5-HT3)受体是半胱氨酸环超家族典型的配体门控离子通道,通过血清素(5-HT)结合激活。该蛋白结合位点的模型揭示了5-HT与酪氨酸143(Tyr143)、酪氨酸153(Tyr153)和酪氨酸234(Tyr234)之间的潜在相互作用。在此,我们基于密度泛函理论描述了一系列从头计算,以评估这些酪氨酸残基突变对5-HT结合的影响。测试了先前实验研究的一系列针对这些酪氨酸的突变,并将结合能与现有实验数据进行比较。我们的结果表明,Tyr153可与5-HT的叔胺形成氢键;该位置的突变显示出的结合能与实验测定的半数有效浓度(EC50)大致相符。Tyr143也可形成氢键,但由于EC50与结合能无关,所以此处不太可能形成这样的键。Tyr234相当独特,它可能通过混合氢键/阳离子-π相互作用与5-HT相互作用。