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Capillary electrophoresis frontal analysis for characterization of alpha(v)beta(3) integrin binding interactions

机译:毛细管电泳额叶分析,用于表征α(v)β(3)整合素结合相互作用

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摘要

The specific binding characteristics of alpha(v)beta(3) integrins with an arginine-glycine-aspartic-acid (RGD) containing fluorescently labeled cyclic peptide is investigated with capillary electrophoresis-frontal analysis method. The new algorithm used to calculate the binding constants and binding stoichiometry was derived without the assumptions made in the commonly used Scatchard Plot method, thus enabling the determination of specific binding parameters in the presence of nonspecific binding. The a,6,3 integrin, a membrane protein, was studied in solution, without the need of immobilization or any other kind of modification. An RGD containing fluorescently labeled cyclic pentapeptide is used as the ligand with both specific and nonspecific binding characteristics, and an arginine-alanine-aspartic-acid (RAD) containing peptide is used as the control for nonspecific binding. While a typical specific binding isotherm has a shape of a rectangular hyperbola, a nonspecific binding isotherm is linear in the same ligand concentration region. A 1:2 specific binding stoichiometry was revealed with the second binding having a similar affinity compared to the first binding event.
机译:通过毛细管电泳-额叶分析方法研究了α(v)β(3)整合素与含有荧光标记的环肽的精氨酸-甘氨酸-天冬氨酸(RGD)的特异性结合特性。无需使用常用的Scatchard Plot方法进行假设即可得出用于计算结合常数和结合化学计量的新算法,从而可以在存在非特异性结合的情况下确定特异性结合参数。在溶液中研究了a,6,3整联蛋白(一种膜蛋白),不需要固定化或任何其他类型的修饰。含有荧光标记的环状五肽的RGD用作具有特异性和非特异性结合特征的配体,并且含有精氨酸-丙氨酸-天冬氨酸(RAD)的肽用作非特异性结合的对照。尽管典型的特异性结合等温线具有矩形双曲线的形状,但是非特异性结合等温线在相同的配体浓度区域中是线性的。揭示了1:2的特异性结合化学计量关系,与第一次结合事件相比,第二次结合具有相似的亲和力。

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