Institute of Polymer Science, University of Ulm, Albert-Einstein-Allee 47, D-89069 Ulm, Germany.
Beilstein J Nanotechnol. 2011;2:525-44. doi: 10.3762/bjnano.2.57. Epub 2011 Sep 5.
In this minireview, we survey recent advances in the synthesis, characterization, and modeling of new oligothiophene-oligopeptide hybrids capable of forming nanostructured fibrillar aggregates in solution and on solid substrates. Compounds of this class are promising for applications because their self-assembly and stimuli-responsive properties, provided by the peptide moieties combined with the semiconducting properties of the thiophene blocks, can result in novel opportunities for the design of advanced smart materials. These bio-inspired molecular hybrids are experimentally shown to form stable fibrils as visualized by AFM and TEM. While the experimental evidence alone is not sufficient to reveal the exact molecular organization of the fibrils, theoretical approaches based on quantum chemistry calculations and large-scale atomistic molecular dynamics simulations are attempted in an effort to reveal the structure of the fibrils at the nanoscale. Based on the combined theoretical and experimental analysis, the most likely models of fibril formation and aggregation are suggested.
在这篇综述中,我们调查了新的寡聚噻吩-寡肽杂化物的合成、表征和建模方面的最新进展,这些杂化物能够在溶液中和固体基底上形成纳米结构的纤维状聚集体。由于这些化合物的自组装和刺激响应特性,由肽部分与噻吩块的半导体性质相结合提供,可能为设计先进的智能材料提供新的机会,因此它们在应用方面具有很大的前景。实验表明,这些生物启发的分子杂化物可以形成稳定的纤维,这可以通过 AFM 和 TEM 观察到。虽然仅凭实验证据不足以揭示纤维的确切分子组织,但我们尝试了基于量子化学计算和大规模原子分子动力学模拟的理论方法,以努力揭示纳米尺度上纤维的结构。基于理论和实验分析的综合结果,提出了纤维形成和聚集的最可能的模型。