School of Chemistry and Chemical Engineering , Shanghai Jiao Tong University , Shanghai 200240 , P. R. China.
Department of Chemistry , University of Utah , 315 South 1400 East, Room 2020 , Salt Lake City , Utah 84112 , United States.
J Am Chem Soc. 2019 Jun 19;141(24):9673-9679. doi: 10.1021/jacs.9b03885. Epub 2019 Jun 7.
The intrinsic relationship between the properties of green fluorescent protein (GFP) and its encapsulated small molecular light machine has spurred many biomimicking studies, aiming at revealing the detailed mechanism and further promoting its wide applications in different disciplines. However, how to build a similar confined microenvironment to mimic the cavity of a β-barrel and the fluorescence turn-on process is a fundamental challenge for both chemists and biologists. Herein, two distinct exo- and endo-functionalized tetraphenylethylene (TPE)-based ML nanospheres with precise distribution of anchored TPE moieties and unique photophysical properties were constructed by means of a coordination-driven self-assembly strategy. Under dilute conditions, the nanospheres fluoresce more strongly than the corresponding TPE subcomponents. Meanwhile, the endo-functionalized sphere is able to induce a higher local concentration and more restrained motion of the enclosed 24 TPE units compared with exo-functionalized counterpart and thus induces much stronger emission due to the restriction of the rotation of the pendant TPE units. The biomimetic methodology developed here represents a promising way to understand and construct artificial GFP materials on the platforms of supramolecular coordination complexes.
绿色荧光蛋白(GFP)的性质与其包裹的小分子光机之间的内在关系激发了许多仿生研究,旨在揭示其详细的机制,并进一步促进其在不同学科中的广泛应用。然而,如何构建类似的受限微环境来模拟β-桶的腔和荧光开启过程,是化学家和生物学家共同面临的基本挑战。在此,我们通过配位驱动的自组装策略,构建了两种具有独特光物理性质的不同的外消旋和内消旋四苯乙烯(TPE)基 ML 纳米球,其中 TPE 部分的连接位置精确可控。在稀溶液条件下,纳米球的荧光强度强于相应的 TPE 亚组分。同时,与外消旋纳米球相比,内消旋纳米球能够诱导被包裹的 24 个 TPE 单元具有更高的局部浓度和更受限制的运动,从而由于侧挂 TPE 单元的旋转受限而导致更强的发射。这里开发的仿生方法代表了一种在超分子配位配合物平台上理解和构建人工 GFP 材料的有前途的方法。