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荧光多糖的制备与性质

Preparation and properties of fluorescent polysaccharides.

作者信息

Glabe C G, Harty P K, Rosen S D

出版信息

Anal Biochem. 1983 Apr 15;130(2):287-94. doi: 10.1016/0003-2697(83)90590-0.

Abstract

A new method for preparing fluorescein derivatives of polysaccharides is described. These derivatives are prepared by activation of the polysaccharide with cyanogen bromide and subsequent reaction with fluoresceinamine. The optimum conditions for coupling have been established in this report. Using this procedure, we have prepared fluorescein derivatives of a wide variety of polysaccharides. Degrees of substitution in the range of 3.0 X 10(-3) to 2.4 X 10(-2) mol of fluorescein per mole of monosaccharide equivalent were obtained. The fluorescent derivatives are stable: no free fluorescein was detected after incubation at 22 degrees C for 48 h or at -10 degrees C for 4 months. The fluorescein-derivatized polysaccharides were found to have the same potency in inhibiting lectin-mediated hemagglutination as the underivatized polysaccharide. In addition, these fluorescent polysaccharides can be radioiodinated to specific activities exceeding 10(6) dpm/micrograms due to incorporation of 125I into fluorescein. The cell binding properties of 125I-fucoidin and 125I-heparin are indistinguishable from the corresponding underivatized polysaccharides. This general approach for preparing fluorescent polysaccharides should produce useful reagents for localizing and quantifying cell surface carbohydrate-binding proteins (lectins).

摘要

本文描述了一种制备多糖荧光素衍生物的新方法。这些衍生物是通过用溴化氰活化多糖,随后与荧光胺反应来制备的。本报告中确定了偶联的最佳条件。使用该方法,我们制备了多种多糖的荧光素衍生物。每摩尔单糖当量的荧光素取代度在3.0×10⁻³至2.4×10⁻²摩尔范围内。荧光衍生物很稳定:在22℃孵育48小时或在-10℃保存4个月后未检测到游离荧光素。发现荧光素衍生化的多糖在抑制凝集素介导的血凝方面与未衍生化的多糖具有相同的效力。此外,由于125I掺入荧光素中,这些荧光多糖可以被放射性碘化至比活超过10⁶dpm/μg。125I-岩藻糖胶和125I-肝素的细胞结合特性与相应的未衍生化多糖没有区别。这种制备荧光多糖的通用方法应该能产生用于定位和定量细胞表面碳水化合物结合蛋白(凝集素)的有用试剂。

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