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DMSO effects on FRET to dye-labeled DNA in conjugated polymer-based DNA detection

机译:DMSO在基于共轭聚合物的DNA检测中对染料标记的DNA的FRET的影响

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Solvent effects were studied in fluorescence resonance energy transfer (FRET) from a cationic polyfluorene copolymer (FHQ, FPQ) to a fluorescein (Fl)-labeled oligonucleotide (ssDNA-Fl). Upon addition of dimethyl sulfoxide (DMSO), optical properties of the polymers and the probe dye were substantially modified. And the FRET-induced Fl emission was measured by directly exciting the polymer within the complex, polymer/ssDNA-Fl. The FRET signal was successfully modulated with changing the DMSO content. In the case of FHQ, the FRET-induced Fl emission was seriously quenched in phosphate buffer solution (PBS), while a salient FRET signal was observed in a 80 vol% DMSO/PBS mixture (36.8 time higher than that in PBS). The FPQ-sensitized FRET signal was also 3.8-fold amplified by the presence of DMSO. That result is from the decrease of hydrophobic interactions between the polymer and ssDNA-Fl, which induces the weaker polymer/ssDNA-Fl complexation with longer intermolecular separation. The gradual decrease in Fl PL quenching with increasing the DMSO content was investigated by measuring the Stern-Volmer quenching constants (3.3-4.2 x 10~6 M~(-1) in PBS, 0.56-1.1 x 10~6 M~(-1) in 80 vol% DMSO) in PBS/DMSO mixtures. The substantially reduced PL quenching would amplify the resulting FRET Fl signal. This approach suggests a simple way of modifying the fine-structure of polymer/ssDNA-Fl and improving the detection sensitivity in conjugated polymer-based FRET bioassays.
机译:研究了从阳离子聚芴共聚物(FHQ,FPQ)到荧光素(F1)标记的寡核苷酸(ssDNA-F1)的荧光共振能量转移(FRET)中的溶剂效应。添加二甲基亚砜(DMSO)后,聚合物和探针染料的光学性能得到了显着改善。通过直接激发复合物中的聚合物/ ssDNA-F1来测量FRET诱导的F1发射。通过更改DMSO含量,成功调制了FRET信号。在FHQ的情况下,在磷酸盐缓冲溶液(PBS)中严重抑制了FRET诱导的Fl发射,而在80%体积的DMSO / PBS混合物中观察到了显着的FRET信号(比PBS高36.8倍)。由于存在DMSO,FPQ敏感的FRET信号也被放大了3.8倍。该结果是由于聚合物与ssDNA-F1之间的疏水相互作用的降低,其导致较弱的聚合物/ ssDNA-F1复合以及更长的分子间分离。通过测量PBS中的Stern-Volmer猝灭常数(3.3-4.2 x 10〜6 M〜(-1),0.56-1.1 x 10〜6 M〜(- 1)在PBS / DMSO混合物中的80 vol%DMSO中。基本上减少的PL猝灭将放大所得的FRET Fl信号。该方法提出了修饰聚合物/ ssDNA-F1的精细结构并提高基于共轭聚合物的FRET生物测定中检测灵敏度的简单方法。

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