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香草醛和乙基香草醛与小牛胸腺 DNA 的沟槽结合。

Groove Binding of Vanillin and Ethyl Vanillin to Calf Thymus DNA.

机构信息

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, 330047, China.

School of Biological Sciences, The University of Auckland, Auckland, 1142, New Zealand.

出版信息

J Fluoresc. 2017 Sep;27(5):1815-1828. doi: 10.1007/s10895-017-2119-x. Epub 2017 May 25.

Abstract

Vanillin (VAN) and ethyl vanillin (EVA) are widely used food additives as flavor enhancers, but may have a potential security risk. In this study, the properties of binding of VAN or EVA with calf thymus DNA (ctDNA) were characterized by multi-spectroscopic methods, multivariate curve resolution-alternating least-squares (MCR-ALS) algorithm and molecular simulation. The concentration profiles for the components (VAN or EVA, ctDNA and VAN-ctDNA or EVA-ctDNA complex) by the MCR-ALS analysis showed that VAN or EVA interacted with ctDNA and formed VAN-ctDNA or EVA-ctDNA complex. The groove binding of VAN or EVA to ctDNA was supported by the results from viscosity measurements, melting studies, denaturation experiments, and competitive binding investigations. Analysis of the Fourier transform infrared spectra corroborated the prediction by molecular docking that VAN and EVA preferentially bound to thymine bases region of ctDNA. The circular dichroism and DNA cleavage assays indicated that both VAN and EVA induced conformational change (from B - like DNA structure toward to A - like form), but didn't lead to a significant damage on DNA. The fluorescence quenching of Hoechst 33,258-ctDNA complex by VAN or EVA was a static quenching, and hydrogen bonding and van der Waals forces were main forces. This study has provided insights into the mechanism of interaction between VAN or EVA with ctDNA, and may also help better understand their potential toxicity with regard to food safety. Graphical Abstract VAN or EVA binds to A-T rich regions of ctDNA in the minor groove.

摘要

香草醛(VAN)和乙基香草醛(EVA)是广泛用作风味增强剂的食品添加剂,但可能存在潜在的安全风险。在这项研究中,通过多光谱方法、多元曲线分辨交替最小二乘法(MCR-ALS)算法和分子模拟研究了 VAN 或 EVA 与小牛胸腺 DNA(ctDNA)结合的性质。通过 MCR-ALS 分析得到的组分浓度图谱(VAN 或 EVA、ctDNA 和 VAN-ctDNA 或 EVA-ctDNA 复合物)表明,VAN 或 EVA 与 ctDNA 相互作用形成 VAN-ctDNA 或 EVA-ctDNA 复合物。粘度测量、熔融研究、变性实验和竞争结合研究结果支持了 VAN 或 EVA 与 ctDNA 的沟结合。傅里叶变换红外光谱分析证实了分子对接预测的 VAN 和 EVA 优先结合 ctDNA 的胸腺嘧啶碱基区域。圆二色性和 DNA 切割实验表明,VAN 和 EVA 均诱导构象变化(从 B 型 DNA 结构向 A 型结构),但不会导致 DNA 明显损伤。VAN 或 EVA 对 Hoechst 33,258-ctDNA 复合物的荧光猝灭是静态猝灭,氢键和范德华力是主要作用力。本研究深入了解了 VAN 或 EVA 与 ctDNA 相互作用的机制,也有助于更好地理解它们在食品安全方面的潜在毒性。

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