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Naphthalene diimide–amino acid conjugates as novel fluorimetric and CD probes for differentiation between ds-DNA and ds-RNA

机译:萘二酰亚胺 - 氨基酸缀合物作为新型氟化物和CD探针用于DS-DNA和DS-RNA之间的分化

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摘要

Two novel unnatural amino acids, prepared by linking a dicationic purple-coloured and fluorescent naphthalene diimide (NDI) at core position to amino acid side chains of variable length, strongly interacted with ds-DNA/RNA by threading intercalation. Different from a reference NDI dye with identical visible range absorbance (520–540 nm) and Stokes shifts in emission (+60 nm, quantum yield > 0.2), only these amino acid–NDI conjugates showed selective fluorimetric response for GC-DNA in respect to AT(U)-polynucleotides. The DNA/RNA binding-induced circular dichroism (ICD) response of NDI at 450–550 nm strongly depended on the length and rigidity of the linker to the amino acid unit, which controls the orientation of the NDI unit inside within the intercalative binding site. The ICD selectivity also depends on the type of polynucleotide, thus the studied NDI dyes act as dual fluorimetric/ICD probes for sensing the difference between here used GC-DNA, AT-DNA and AU-RNA.
机译:通过将核心位置连接到可变长度的氨基酸侧链,通过将DS-DNA / RNA连接到核酸侧链,通过将DS-DNA / RNA连接到可变长度的氨基酸侧链来制备两种新型非天然氨基酸。与具有相同可见范围吸光度(520-540nm)和斯托克斯在发射时(+ 60nm,量子产率> 0.2)的斯托克斯偏移的不同,只有这些氨基酸-NDI缀合物对GC-DNA表示的选择性荧光反应在(U)-polynoc核苷酸。 NDI的DNA / RNA结合诱导的圆形二色(ICD)响应强烈依赖于接头与氨基酸单元的长度和刚度,其控制内部粘结位点内的NDI单元的取向。 ICD选择性还取决于多核苷酸的类型,因此研究的NDI染料充当双荧光/ ICD探针,用于感测在这里使用的GC-DNA,AT-DNA和Au-RNA之间的差异。

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