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Theoretical Evidence for the Stronger Ability of Thymine to Disperse SWCNT than Cytosine and Adenine: self-stacking of DNA bases vs their cross-stacking with SWCNT

机译:胸腺嘧啶比胞嘧啶和腺嘌呤具有更强的分散SWCNT能力的理论证据:DNA碱基的自堆积与它们与SWCNT的交叉堆积

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摘要

Self-stacking of four DNA bases, adenine (A), cytosine (C), guanine (G) and thymine (T), and their cross-stacking with (5,5) as well as (10,0) single walled carbon nanotubes (SWCNTs) were extensively investigated with a novel hybrid DFT method, MPWB1K/cc-pVDZ. The binding energies were further corrected with MP2/6-311++G(d,p) method in both gas phase and aqueous solution, where the solvent effects were included with conductor-like polarized continuum model (CPCM) model and UAHF radii. The strongest self-stacking of G and A takes displaced anti-parallel configuration, but un-displaced or “eclipsed” anti-parallel configuration is the most stable for C and T. In gas phase the self-stacking of nucleobases decreases in the sequence G>A>C>T, while because of quite different solvent effects their self-stacking in aqueous solution exhibits a distinct sequence A>G>T>C. For a given base, cross-stacking is stronger than self-stacking in both gas phase and aqueous solution. Binding energy for cross-stacking in gas phase varies as G>A>T>C for both (10,0) and (5,5) SWCNTs, and the binding of four nucleobases to (10,0) is slightly stronger than to (5,5) SWCNT by a range of 0.1–0.5 kcal/mol. The cross-stacking in aqueous solution varies differently from that gas phase: A>G>T>C for (10,0) SWCNT and G>A>T>C for (5,5) SWCNT. It is suggested that the ability of nucleobases to disperse SWCNT depends on relative strength (ΔΔEbinsol) of self-stacking and cross-stacking with SWCNT in aqueous solution. Of the four investigated nucleobases thymine (T) exhibits the highest (ΔΔEbinsol) which can well explain the experimental finding that T more efficiently functionalizes SWCNT than C and A.
机译:四个DNA碱基,腺嘌呤(A),胞嘧啶(C),鸟嘌呤(G)和胸腺嘧啶(T)的自堆叠,以及与(5,5)和(10,0)单壁碳的交叉堆叠纳米碳管(SWCNTs)已通过新型混合DFT方法MPWB1K / cc-pVDZ进行了广泛研究。在气相和水溶液中,用MP2 / 6-311 ++ G(d,p)方法进一步校正了结合能,其中溶剂效应包括在导体样极化连续谱模型(CPCM)模型和UAHF半径中。 G和A的最强自堆积具有位移的反平行构型,但对于C和T,最稳定的“位移”或“蚀”反平行构型。在气相中,核碱基的自堆积在序列中减少G> A> C> T,尽管由于溶剂作用的差异很大,它们在水溶液中的自堆积表现出不同的序列A> G> T> C。对于给定的碱,在气相和水溶液中交叉堆积都比自堆积更强。气相交叉堆积的结合能随(10,0)和(5,5)SWCNT的G> A> T> C的变化而变化,并且四个核碱基与(10,0)的结合略强于(5,5)SWCNT的范围为0.1–0.5 kcal / mol。水溶液中的交叉堆积与气相的变化有所不同:(1,0)SWCNT的A> G> T> C,(5,5)SWCNT的G> A> T> C。建议核碱基分散SWCNT的能力取决于相对强度 < mrow> Δ Δ E bin sol 与SWCNT在水溶液中的自堆叠和交叉堆叠。在四个被研究的核碱基中,胸腺嘧啶(T)表现出最高的 < mo Stretchy =“ false”>( Δ Δ E < mrow> bin sol 可以很好地解释实验结果,即T比C和A更有效地功能化SWCNT。

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    Yixuan Wang;

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  • 年(卷),期 -1(112),37
  • 年度 -1
  • 页码 14297–14305
  • 总页数 21
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