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Symmetric and asymmetric squarylium dyes as noncovalent protein labels: a study by fluorimetry and capillary electrophoresis

机译:对称和不对称方酸染料作为非共价蛋白标记:通过荧光法和毛细管电泳进行的研究

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Noncovalent interactions between two squarylium dyes and various model proteins have been explored. NN127 and SQ-3 are symmetric and asymmetric squarylium dyes, respectively, the fluorescence emissions of which have been shown to be enhanced upon complexation with proteins such as bovine serum albumin (BSA), human serum albumin (HSA), β-lactoglobulin A, and trypsinogen. Although these dyes are poorly soluble in aqueous solution, they can be dissolved first in methanol followed by dilution with aqueous buffer without precipitation, and are then suitable for use as fluorescent labels in protein determination studies. The nature of interactions between these dyes and proteins was studied using a variety of buffer systems, and it was found that electrostatic interactions are involved but not dominant. Dye/protein stoichiometries in the noncovalent complexes were found to be 1:1 for SQ-3, although various possible stoichiometries were found for NN127 depending upon pH and protein. Association constants on the order of 10~5 and 10~7 were found for noncovalent complexes of SQ-3 and NN127, respectively, with HSA, indicating stronger interactions of the symmetric dye with proteins. Finally, HSA complexes with NN127 were determined by capillary electrophoresis with laser-induced fluorescence detection (CE-LIF). In particular, NN127 shows promise as a reagent capable of fluorscently labeling analyte proteins for analysis by CE-LIF without itself being significantly fluorescent under the aqueous solution conditions studied herein.
机译:已经探究了两种方酸染料与各种模型蛋白之间的非共价相互作用。 NN127和SQ-3分别是对称和不对称的方酸染料,已经证明与蛋白质结合后,如牛血清白蛋白(BSA),人血清白蛋白(HSA),β-乳球蛋白A,和胰蛋白酶原。尽管这些染料在水溶液中的溶解度很差,但是可以先将它们溶解在甲醇中,然后用水性缓冲液稀释而不沉淀,然后适合用作蛋白质测定研究中的荧光标记。使用各种缓冲液系统研究了这些染料与蛋白质之间相互作用的性质,并且发现静电相互作用涉及但不是主要的。对于SQ-3,发现非共价复合物中的染料/蛋白质化学计量比为1:1,尽管根据pH和蛋白质,发现NN127的各种化学计量比。 SQ-3和NN127与HSA的非共价配合物的缔合常数分别为10〜5和10〜7数量级,表明对称染料与蛋白质的相互作用更强。最后,通过毛细管电泳和激光诱导荧光检测(CE-LIF)来测定HSA与NN127的配合物。尤其是,NN127有望成为一种试剂,该试剂能够荧光标记分析物蛋白质以用于CE-LIF分析,而其本身在本文研究的水溶液条件下不会显着发荧光。

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