Oxford J S, Schild G C
J Gen Virol. 1978 Jan;38(1):187-93. doi: 10.1099/0022-1317-38-1-187.
The major influenza A virus structural antigens, matrix protein, nucleoprotein, haemagglutinin and neuraminidase were measured rapidly and accurately using a rocket immunoelectrophoresis technique. Virus was disrupted with 1% (w/v) sodium sarcosyl and electrophoresed into agarose containing specific antiserum to the individual virus structural proteins in 0.05 M-barbitone buffer, pH 8.6, for 1 to 4 h. For haemagglutinin antigen assays statistical analysis indicated that the coefficient of variation within an immunoelectrophoresis plate was 8.0% for antigen concentrations in the range 15 to 40 microgram/ml protein. For haemagglutinin and matrix protein the method was sufficiently sensitive to measure concentrations of antigens as low as 1.5 and 2.0 microgram/ml respectively. By incorporation in the agarose of mixtures of antisera against specific antigens of the virus, haemagglutinin, matrix or nucleoprotein could be assayed simultaneously.
利用火箭免疫电泳技术可快速、准确地检测甲型流感病毒的主要结构抗原,即基质蛋白、核蛋白、血凝素和神经氨酸酶。用1%(w/v)的十二烷基肌氨酸钠裂解病毒,并在pH 8.6的0.05M巴比妥缓冲液中,于含针对各病毒结构蛋白的特异性抗血清的琼脂糖中电泳1至4小时。对于血凝素抗原检测,统计分析表明,在免疫电泳板内,当抗原浓度在15至40微克/毫升蛋白质范围内时,变异系数为8.0%。对于血凝素和基质蛋白,该方法灵敏度足够高,分别可检测低至1.5和2.0微克/毫升的抗原浓度。通过在琼脂糖中加入针对病毒特定抗原的抗血清混合物,可同时检测血凝素、基质或核蛋白。