School of Pharmacy and Pharmaceutical Sciences and ‡School of Chemistry, University of Manchester , Oxford Road, Manchester M13 9PT, U.K.
Biochemistry. 2013 May 28;52(21):3740-51. doi: 10.1021/bi301112p. Epub 2013 May 14.
Trypanosoma cruzitrans-sialidase (TcTS), which catalyzes the transfer or hydrolysis of terminal sialic acid residues, is crucial to the development and proliferation of the T. cruzi parasite and thus has emerged as a potential drug target for the treatment of Chagas disease. We here probe the origin of the observed preference for the transfer reaction over hydrolysis where the substrate for TcTS is the natural sialyl donor (represented in this work by sialyllactose). Thus, acceptor lactose preferentially attacks the sialyl-enyzme intermediate rather than water. We compare this with the weaker preference for such transfer shown by a synthetic donor substrate, 4-methylumbelliferyl α-d-acetylneuraminide. For this reason, we conducted molecular dynamics simulations of TcTS following its sialylation by the substrate to examine the behavior of the asialyl leaving group by the protein. These simulations indicate that, where lactose is released, this leaving group samples well-defined interactions in the acceptor site, some of which are mediated by localized water molecules; also, the extent of the opening of the acceptor site to solvent is reduced as compared with those of unliganded forms of TcTS. However, where there is release of 4-methylumbelliferone, this leaving group explores a range of transient poses; surrounding active site water is also more disordered. The acceptor site explores more open conformations, similar to the case in which the 4-methylumbelliferone is absent. Thus, the predicted solvent accessibility of sialylated TcTS is increased when 4-methylumbelliferyl α-d-acetylneuraminide is the substrate compared to sialyllactose; this in turn is likely to contribute to a greater propensity for hydrolysis of the covalent intermediate. These computational simulations, which suggest that protein flexibility has a role in the transferase/sialidase activity of TcTS, have the potential to aid in the design of anti-Chagas inhibitors effective against this neglected tropical disease.
克氏锥虫唾液酸转移酶(TcTS)能够催化末端唾液酸残基的转移或水解,对于克氏锥虫寄生虫的发育和增殖至关重要,因此已成为治疗恰加斯病的潜在药物靶点。在这里,我们探究了观察到的对转移反应的偏好的起源,其中 TcTS 的底物是天然唾液酸供体(在本工作中由唾液乳糖表示)。因此,受体乳糖更倾向于攻击唾液酰-酶中间产物,而不是水。我们将这与合成供体底物 4-甲基伞形酮基-α-d-乙酰神经氨酸对这种转移的较弱偏好进行了比较。因此,我们对 TcTS 进行了分子动力学模拟,模拟了其被底物唾液酸化后的行为,以检查蛋白质中无唾液酸离去基团的行为。这些模拟表明,当释放乳糖时,该离去基团在受体位点中很好地定义了相互作用,其中一些是由局部水分子介导的;此外,与 TcTS 未配位形式相比,受体位点对溶剂的开放程度降低。然而,当释放 4-甲基伞形酮时,该离去基团探索了一系列瞬态构象;周围的活性位点水也更加无序。受体位点探索更开放的构象,类似于不存在 4-甲基伞形酮的情况。因此,与唾液乳糖相比,当 4-甲基伞形酮基-α-d-乙酰神经氨酸为底物时,预测的 TcTS 唾液酸化的溶剂可及性增加;这反过来又可能导致共价中间产物水解的倾向增加。这些计算模拟表明,蛋白质的灵活性在 TcTS 的转移酶/唾液酸酶活性中起着作用,有可能有助于设计针对这种被忽视的热带病的有效的抗恰加斯抑制剂。