Reichau Sebastian, Blackmore Nicola J, Jiao Wanting, Parker Emily J
Biomolecular Interaction Centre and Department of Chemistry, University of Canterbury, Christchurch, New Zealand.
PLoS One. 2016 Apr 29;11(4):e0152723. doi: 10.1371/journal.pone.0152723. eCollection 2016.
Chirality plays a major role in recognition and interaction of biologically important molecules. The enzyme 3-deoxy-d-arabino-heptulosonate 7-phosphate synthase (DAH7PS) is the first enzyme of the shikimate pathway, which is responsible for the synthesis of aromatic amino acids in bacteria and plants, and a potential target for the development of antibiotics and herbicides. DAH7PS from Mycobacterium tuberculosis (MtuDAH7PS) displays an unprecedented complexity of allosteric regulation, with three interdependent allosteric binding sites and a ternary allosteric response to combinations of the aromatic amino acids l-Trp, l-Phe and l-Tyr. In order to further investigate the intricacies of this system and identify key residues in the allosteric network of MtuDAH7PS, we studied the interaction of MtuDAH7PS with aromatic amino acids that bear the non-natural d-configuration, and showed that the d-amino acids do not elicit an allosteric response. We investigated the binding mode of d-amino acids using X-ray crystallography, site directed mutagenesis and isothermal titration calorimetry. Key differences in the binding mode were identified: in the Phe site, a hydrogen bond between the amino group of the allosteric ligands to the side chain of Asn175 is not established due to the inverted configuration of the ligands. In the Trp site, d-Trp forms no interaction with the main chain carbonyl group of Thr240 and less favourable interactions with Asn237 when compared to the l-Trp binding mode. Investigation of the MtuDAH7PSN175A variant further supports the hypothesis that the lack of key interactions in the binding mode of the aromatic d-amino acids are responsible for the absence of an allosteric response, which gives further insight into which residues of MtuDAH7PS play a key role in the transduction of the allosteric signal.
手性在生物重要分子的识别和相互作用中起着重要作用。3-脱氧-d-阿拉伯庚酮糖酸-7-磷酸合酶(DAH7PS)是莽草酸途径的第一个酶,负责细菌和植物中芳香族氨基酸的合成,是抗生素和除草剂开发的潜在靶点。结核分枝杆菌的DAH7PS(MtuDAH7PS)表现出前所未有的变构调节复杂性,具有三个相互依赖的变构结合位点以及对芳香族氨基酸l-Trp、l-Phe和l-Tyr组合的三元变构响应。为了进一步研究该系统的复杂性并确定MtuDAH7PS变构网络中的关键残基,我们研究了MtuDAH7PS与具有非天然d-构型的芳香族氨基酸的相互作用,结果表明d-氨基酸不会引发变构响应。我们使用X射线晶体学、定点诱变和等温滴定量热法研究了d-氨基酸的结合模式。确定了结合模式的关键差异:在Phe位点,由于配体构型反转,变构配体的氨基与Asn175侧链之间未形成氢键。在Trp位点,与l-Trp结合模式相比,d-Trp与Thr240的主链羰基没有相互作用,与Asn237的相互作用也不太有利。对MtuDAH7PSN175A变体的研究进一步支持了以下假设,即芳香族d-氨基酸结合模式中缺乏关键相互作用导致变构响应缺失,这进一步深入了解了MtuDAH7PS的哪些残基在变构信号转导中起关键作用。