Department of Chemistry, University of Washington, Seattle, Washington 98195-1700, USA.
J Am Chem Soc. 2013 Aug 7;135(31):11453-6. doi: 10.1021/ja404719f. Epub 2013 Jul 29.
Much work has been done on collapsed chains of conjugated semiconducting polymers and their applications as fluorescent probes or sensors. On surfaces spin-coated with semiconducting polymers, excitation energy transfer along the polymer backbone can be used to quickly and efficiently funnel energy to chromophores with localized energy minima. If each chromophore is immobilized within its matrix, this can result in a large fluorescence anisotropy. Through nanoprecipitation of a matrix polymer blended at low mass ratios with short-chain, hydrophobic, fluorescent semiconducting polymers, we took advantage of this large fluorescence anisotropy to make polarization-sensitive nanoparticles (NPs). These NPs are small (~7 nm in diameter), exhibit a high quantum yield of 0.75, and are easily functionalized to bind to protein targets. Excitation of the NPs with polarized light on a wide-field fluorescence microscope enabled monitoring of both protein location and changes in protein orientation.
在已坍塌的共轭半导体聚合物链及其作为荧光探针或传感器的应用方面,已经开展了大量的工作。在通过旋涂法在表面上涂覆半导体聚合物后,聚合物主链上的激发能量转移可用于快速有效地将能量传递到具有局部能量极小值的发色团。如果每个发色团都固定在其基质内,这可能导致大的荧光各向异性。通过在低质量比下将基质聚合物与短链、疏水性、荧光半导体聚合物共混进行纳米沉淀,我们利用这种大的荧光各向异性来制备对偏振敏感的纳米颗粒(NPs)。这些 NPs 尺寸较小(~7nm 直径),量子产率高达 0.75,并且易于功能化以与蛋白质靶标结合。在宽场荧光显微镜上用偏振光激发 NPs,可以监测蛋白质的位置和蛋白质取向的变化。