Kann Nina, Johansson Johan R, Beke-Somfai Tamás
Department of Chemical and Biological Engineering, Chalmers University of Technology, SE-41296 Göteborg, Sweden.
Org Biomol Chem. 2015 Mar 7;13(9):2776-85. doi: 10.1039/c4ob02359e.
Peptidic foldamers have recently emerged as a novel class of artificial oligomers with properties and structural diversity similar to that of natural peptides, but possessing additional interesting features granting them great potential for applications in fields from nanotechnology to pharmaceuticals. Among these, foldamers containing 1,4- and 1,5-substitued triazole amino acids are easily prepared via the Cu- and Ru-catalyzed click reactions and may offer increased side chain variation, but their structural capabilities have not yet been widely explored. We here describe a systematic analysis of the conformational space of the two most important basic units, the 1,4-substitued (4Tzl) and the 1,5-substitued (5Tzl) 1,2,3-triazole amino acids, using quantum chemical calculations and NMR spectroscopy. Possible conformations of the two triazoles were scanned and their potential minima were located using several theoretical approaches (B3LYP/6-311++G(2d,2p), ωB97X-D/6-311++G(2d,2p), M06-2X/6-311++G(2d,2p) and MP2/6-311++G(2d,2p)) in different solvents. BOC-protected versions of 4Tzl and 5Tzl were also prepared via one step transformations and analyzed by 2D NOESY NMR. Theoretical results show 9 conformers for 5Tzl derivatives with relative energies lying close to each other, which may lead to a great structural diversity. NMR analysis also indicates that conformers preferring turn, helix and zig-zag secondary structures may coexist in solution. In contrast, 4Tzl has a much lower number of conformers, only 4, and these lack strong intraresidual interactions. This is again supported by NMR suggesting the presence of both extended and bent conformers. The structural information provided on these building units could be employed in future design of triazole foldamers.
肽类折叠体最近已成为一类新型的人工低聚物,其性质和结构多样性与天然肽类似,但具有其他有趣的特征,使其在从纳米技术到制药等领域具有巨大的应用潜力。其中,含有1,4-和1,5-取代三唑氨基酸的折叠体可通过铜催化和钌催化的点击反应轻松制备,并且可能提供更多的侧链变化,但其结构能力尚未得到广泛探索。我们在此描述了使用量子化学计算和核磁共振光谱对两个最重要的基本单元,即1,4-取代(4Tzl)和1,5-取代(5Tzl)的1,2,3-三唑氨基酸的构象空间进行的系统分析。使用几种理论方法(B3LYP/6-311++G(2d,2p)、ωB97X-D/6-311++G(2d,2p)、M06-2X/6-311++G(2d,2p)和MP2/6-311++G(2d,2p))在不同溶剂中扫描了两种三唑的可能构象,并确定了它们的潜在极小值。4Tzl和5Tzl的BOC保护版本也通过一步转化制备,并通过二维NOESY核磁共振进行分析。理论结果表明,5Tzl衍生物有9种构象,其相对能量彼此接近,这可能导致很大的结构多样性。核磁共振分析还表明,倾向于转角、螺旋和锯齿形二级结构的构象可能在溶液中共存。相比之下,4Tzl的构象数量要少得多,只有4种,并且这些构象缺乏强烈的残基内相互作用。核磁共振再次支持了这一点,表明存在伸展和弯曲的构象。这些构建单元提供的结构信息可用于未来三唑折叠体的设计。