Dipartimento di Chimica and IMC - CNR Sezione Meccanismi di Reazione, Università La Sapienza , 00185 Roma, Italy.
Dipartimento di Chimica, Università degli Studi di Parma , Parco Area delle Scienze 17/a, 43124 Parma, Italy.
J Org Chem. 2016 Jun 3;81(11):4728-35. doi: 10.1021/acs.joc.6b00644. Epub 2016 May 17.
The catalytic activity of an artificial phosphodiesterase that combines a ligated metal ion (Cu(II), Zn(II)) with a guanidinium unit connected by a 1,2-vicinal calix[4]arene spacer was investigated in the transesterification of RNA models HPNP and four diribonucleoside 3',5'-monophosphates. Comparison with previous data related to the 1,3-distal regioisomeric metal complexes confirms the superiority of the Cu(II) complexes over the Zn(II) analogs and shows that in the reactions of HPNP, GpU, and UpU, the catalytic efficiency depends very little on whether the substitution pattern is 1,2-vicinal or 1,3-distal. On the other hand, CpA turned out to be a good substrate for the Cu(II) complex of the 1,2-vicinal catalyst and a bad substrate for the corresponding 1,3-distal regioisomer, whereas the opposite holds for GpA. Extension of the investigation to the cleavage of the DNA model BNPP showed that both Zn(II) and Cu(II) complexes exhibit good catalytic efficiency, with a superiority of the 1,2-vicinal catalyst in both cases. The data reported in this work show that rate accelerations over background for the best catalyst-substrate combinations at 0.5 mM catalyst concentration are 3.6 × 10(5)-fold for HPNP, 1.1 × 10(6)-fold for BNPP, and range from 1.3 × 10(6)- to 1.3 × 10(7)-fold for diribonucleoside monophosphates.
研究了一种人工磷酸二酯酶的催化活性,该酶将连接的金属离子(Cu(II)、Zn(II))与通过 1,2-顺式联吡啶[4]芳烃间隔基连接的胍基单元结合。在 RNA 模型 HPNP 和四种二核糖核苷 3',5'-单磷酸酯的转酯反应中研究了该酶的催化活性。与先前与 1,3-远端区域异构金属配合物相关的数据进行比较,证实了 Cu(II)配合物优于 Zn(II)类似物,并表明在 HPNP、GpU 和 UpU 的反应中,催化效率几乎与取代模式是 1,2-顺式还是 1,3-远端无关。另一方面,CpA 是 1,2-顺式催化剂的 Cu(II)配合物的良好底物,而对于相应的 1,3-远端区域异构体则是不良底物,而 GpA 则相反。将研究扩展到 DNA 模型 BNPP 的切割,结果表明 Zn(II)和 Cu(II)配合物都表现出良好的催化效率,而在两种情况下,1,2-顺式催化剂都具有优势。本工作报道的数据表明,在 0.5 mM 催化剂浓度下,最佳催化剂-底物组合的背景速率加速倍数分别为 HPNP 为 3.6×10(5)倍,BNPP 为 1.1×10(6)倍,二核糖核苷单磷酸酯的范围为 1.3×10(6)倍至 1.3×10(7)倍。