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Time-resolved fluorescence measurements of cyanine dyes in biomimetic systems

机译:仿生体系中青色染料的时间分辨荧光测量

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In the present study the photophysical properties of DY-635B, a cyanine dye, bound to streptavidin were characterized in detail. Special emphasis was given to i) the alterations in the intrinsic photophysical characteristics of the dye due to (un) specific interactions with streptavidin and ii) the evaluation of interaction between the fluorescence probe and streptavidin in the presence of unlabeled biotin. Fluorescence correlation spectroscopy (FCS) and time-resolved anisotropy experiments were carried out in the presence of excess biotin to monitor also a possible cooperative effect on the fluorescence behavior of DY-635B. Based on the evaluation of FCS and time-resolved anisotropy data it is shown that due to binding to streptavidin the rotational freedom of DY-635B is restricted. This restriction is further increased by additional biotin indicating that the biotin binding is altering the tertiary structure of streptavidin. The intrinsic photophysical deactivation processes of DY-635B are changed as well. From FCS measurements it is concluded that due to the specific interaction of DY-635B and streptavidin, the deactivation via a "dark state" becomes less effective, shown as an increase of the corresponding decay time τ_R.
机译:在本研究中DY-635B,花青染料,结合于链霉亲和的光物理性质详细表征。特别强调了与i)中的染料的固有特性光物理由于(用链霉亲未)特异性相互作用,和ii)未标记的生物素的存在下的荧光探针和链霉之间的相互作用的评价改变。荧光相关光谱(FCS)和时间分辨各向异性实验在过量的生物素的存在下也以监测DY-635B的荧光行为的可能的协同作用进行。基于FCS和时间分辨各向异性数据的评估中,示出的是,由于结合于链霉亲和DY-635B的旋转自由度受到限制。此限制进一步增加额外的生物素,表明生物素结合的链霉亲和改变的三级结构。 DY-635B的固有光物理失活过程也改变了。从FCS测量得出的结论是由于DY-635B和链霉的特异性相互作用,经由“暗状态”去激活变得较不有效,示出为增加了相应的衰减时间τ_R。

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