Powell L D, Hart G W
Anal Biochem. 1986 Aug 15;157(1):179-85. doi: 10.1016/0003-2697(86)90211-3.
A simple HPLC adaptation of the periodate-TBA assay for free N-acetyl- and N-glycolylneuraminic acids greatly extends the sensitivity and increases the specificity of this standard colorimetric assay. The method, employing a C18 reverse-phase column eluted isocratically with a phosphoric acid-MeOH buffer, is linear over a range of 2 pmol to 20 nmol. Analyses can be performed directly on cell lysates and digests without prior purification of released sialic acids from contaminating salts and biological materials. Interference from 2-deoxysugars is completely eliminated as the chromophore from these compounds is completely resolved from that derived from sialic acids. The application of the technique to quantify cell-surface and total cellular TBA-reactive sialic acids on the surfaces of a variety of tumor cells is described. Additionally, the extent of desialylation of erythrocytes necessary to expose the T antigen is determined.
对高碘酸盐-TBA法进行简单的HPLC改进,用于检测游离的N-乙酰神经氨酸和N-羟乙酰神经氨酸,极大地提高了这种标准比色法的灵敏度并增强了特异性。该方法采用C18反相柱,用磷酸-甲醇缓冲液等度洗脱,在2 pmol至20 nmol范围内呈线性。分析可直接在细胞裂解物和消化物上进行,无需事先从污染的盐类和生物材料中纯化释放出的唾液酸。2-脱氧糖的干扰被完全消除,因为这些化合物的发色团与唾液酸衍生的发色团完全分离。描述了该技术在定量多种肿瘤细胞表面的细胞表面和总细胞TBA反应性唾液酸方面的应用。此外,还确定了暴露T抗原所需的红细胞去唾液酸化程度。