Influence of PNA containing 8-aza-7-deazaadenine on structure stability and binding affinity of PNA•DNA duplex: insights from thermodynamics, counter ion, hydration and molecular dynamics analysis

摘要

This paper describes the synthesis of a novel 8-aza-7-deazapurin-2,6-diamine (DPP)-containing peptide nucleic acid (PNA) monomer and Boc protecting group-based oligomerization of PNA, replacing adenine (A) with DPP monomers in the PNA strand. The PNA oligomers were synthesized against the biologically relevant SV40 promoter region (2494-AATTTTTTTTATTTA-2508) of pEGFP-N3 plasmid. The DPP-PNA•DNA duplex showed enhanced stability as compared to normal duplex (A-PNA•DNA). The electronic distribution of DPP monomer suggested that DPP had better electron donor properties over 2,6-diamino purine. UV melting and thermodynamic analysis revealed that the PNA oligomer containing a diaminopyrazolo(3,4-d)pyrimidine moiety (DPP) stabilized the PNA•DNA hybrids compared to A-PNA•DNA. DPP-PNA•DNA duplex showed higher water activity (Δn_w = 38.5) in comparison to A-PNA•DNA duplex (Δn_w = 14.5). The 50 ns molecular dynamics simulations of PNA•DNA duplex containing DPP or unmodified nucleobase-A showed average H-bond distances in the DPP-dT base pair of 2.90 Å (O…H-N bond) and 2.91 Å (N…H-N bond), which were comparably shorter than in the A-dT base pair, in which the average distances were 3.18 Å (O…H-N bond) and 2.97 Å (N…H-N bond), and there was one additional H-bond in the DPP-dT base pair of around 2.98 Å (O2…H-N2 bond), supporting the higher stability of DPP-PNA•DNA. The analysis of molecular dynamics simulation data showed that the system binding free energy increased at a rate of approximately -4.5 kcal mol~(-1) per DPP base of the PNA•DNA duplex. In summary, increased thermal stability, stronger hydrogen bonding and more stable conformation in the DPP-PNA•DNA duplex make it a better candidate as antisense/antigene therapeutic agents.