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Biarsenical-Tetracysteine Motif as a Fluorescent Tag for Detection in Capillary Electrophoresis

机译:Biarsenical-Tetracysteine图案作为用于毛细管电泳检测的荧光标签

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Biarsenical dyes complexed to tetracysteine motifs have proven to be highly useful fluorescent dyes in labeling specific cellular proteins for microscopic imaging. Their many advantages include membrane permeability, relatively small size, stoichiometric labeling, high affinity, and an assortment of excitation/emission wavelengths. The goal of the current study was to determine whether the biarsenical labeling scheme could be extended to fluorescent detection of analytes in capillary electrophoresis. Recombinant protein or synthesized peptides containing the optimized tetracysteine motif "-C-C-P-G-C-C-" were labeled with biarsenical dyes and then analyzed by micellar electrokinetic capillary chromatography (MEKC). The biarsenical-tetracysteine complex was stable and remained fluorescent under standard MEKC conditions for peptide and protein separations. The detection limit following electrophoresis in a capillary was less than 3 X 10~(-20) mol with a simple laser-induced fluorescence system. A mixture of multiple biarsenical-labeled peptides and a protein were easily resolved. Demonstrating that the label did not interfere with bioactivity, a peptide-based enzyme substrate conjugated to the tetracysteine motif and labeled with a biarsenical dye retained its ability to be phosphorylated by the parent kinase. The feasibility of using this label for chemical cytometry experiments was shown by intracellular labeling and subsequent analysis of a recombinant protein possessing the tetracysteine motif expressed in living cells. The extension of the biarsenical-tetracysteine tag to fluorescent labeling of peptides and proteins in chemical separations is a valuable addition to biochemical and cell-based investigations.
机译:已证明,与四半胱氨酸基序络合的双砷染料是用于标记特定细胞蛋白以进行显微成像的高度有用的荧光染料。它们的许多优点包括膜渗透性,相对较小的尺寸,化学计量标记,高亲和力以及各种激发/发射波长。当前研究的目的是确定双砷标记方案是否可以扩展到毛细管电泳中分析物的荧光检测。用双砷染料标记包含优化的四半胱氨酸基序“ -C-C-P-G-C-C-”的重组蛋白或合成肽,然后通过胶束电动毛细管色谱法(MEKC)进行分析。双砷-四半胱氨酸复合物是稳定的,并且在用于肽和蛋白质分离的标准MEKC条件下仍保持荧光。使用简单的激光诱导荧光系统,毛细管电泳后的检出限小于3 X 10〜(-20)mol。多个双砷标记的肽和蛋白质的混合物很容易分辨。为了证明标记物不干扰生物活性,缀合到四半胱氨酸基序并被双砷染料标记的基于肽的酶底物保留了其被亲本激酶磷酸化的能力。通过细胞内标记和随后分析具有在活细胞中表达的具有四胱氨酸基序的重组蛋白,证明了将该标记用于化学细胞术实验的可行性。在化学分离中,将Biarsenical-tetracysteine标签扩展到肽和蛋白质的荧光标记是对生物化学和基于细胞的研究的重要补充。

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