Istituto di Biostrutture e Bioimmagini, CNR, Via Mezzocannone 16, 80134, Naples, Italy.
Amino Acids. 2012 Oct;43(4):1615-23. doi: 10.1007/s00726-012-1237-7. Epub 2012 Feb 15.
This work deals with the Dakin-West synthesis, starting from the nucleoamino acid 1-thyminyl acetic acid, as well the NMR, ESI MS, and X-ray characterization of a heteroaromatic compound denominated by us T(2)CO, comprising two thymine moieties anchored to a 2-propanonic unit, the spectroscopic properties of which were studied by UV as a function of temperature and ionic strength. Preliminary binding-studies with molecules of biomedical interest such as nucleic acids and proteins, performed on samples containing T(2)CO, suggested that this molecule is able to interact very weakly with double-stranded RNA, whereas it does not seem to bind other nucleic acids or proteins. Moreover, by studies with fresh human serum we found that T(2)CO is resistant to enzymatic degradation till 24 h, whereas UV metal binding-studies, performed using solutions of copper (II) chloride dihydrate and nickel (II) chloride hexahydrate, revealed a certain ability of T(2)CO to bind copper (II) cation. Finally, by CD spectroscopy we investigated the influence of T(2)CO on the already described supramolecular networks based on L-serine-containing nucleopeptides. More particularly, we found that T(2)CO is able to increase the level of structuration of the non-covalent supramolecular assembly of the chiral nucleopeptides, which is a feature of remarkable interest for the development of innovative drug delivery tools.
这项工作涉及达金-韦斯特合成,从核碱基氨基酸 1-胸腺嘧啶乙酸开始,以及我们命名为 T(2)CO 的杂芳族化合物的 NMR、ESI MS 和 X 射线表征,该化合物由两个胸腺嘧啶部分锚定在 2-丙酰单元上,其光谱性质通过 UV 随温度和离子强度进行了研究。在含有 T(2)CO 的样品上进行了与具有生物医学意义的分子如核酸和蛋白质的初步结合研究,表明该分子能够与双链 RNA 非常弱地相互作用,而似乎不与其他核酸或蛋白质结合。此外,通过对新鲜人血清的研究,我们发现 T(2)CO 能够抵抗酶降解 24 小时,而使用二水合氯化铜(II)和六水合氯化镍(II)溶液进行的 UV 金属结合研究表明,T(2)CO 具有一定的结合铜(II)阳离子的能力。最后,通过 CD 光谱研究,我们调查了 T(2)CO 对基于含有 L-丝氨酸的核肽的已描述的超分子网络的影响。更特别的是,我们发现 T(2)CO 能够增加手性核肽的非共价超分子组装的结构化水平,这是开发创新药物输送工具的显著特征。