Wilson G B, Arnaud P, Fudenberg H H
Pediatr Res. 1977 Sep;11(9 Pt 1):986-9. doi: 10.1203/00006450-197709000-00011.
We have developed an improved method for the detection of cystic fibrosis protein (CFP). The method employs the LKB Multiphor to electrofocus whole serum, instead of the apparatus used in previous studies. Two basic modifications were necessary: (1) a pH 2.5--10.0 gradient instead of a pH 5--10 gradient, and (2) constant power for focusing the serum proteins instead of constant voltage. The first modification ensured adequate dissolution of the CFP-IgG complexes (or other precursor complexes which may liberate CFP). The second modification ensured a linear gradient (between pH 3.8 and pH 9.2), excellent resolution in the pH 8--9 region, and the separation of CFP within 2 hr without overheating of the gel. Electrofocusing with the LKB Multiphor permits the detection of CFP in as many as 24 serum samples per gel. Results obtained from the analysis of 31 cystic fibrosis, 28 obligate heterozygote carrier, and 28 normal control sera indicate that CFP can be reproducibly and accurately detected in sera using the LKB Multiphor.
我们已经开发出一种改进的检测囊性纤维化蛋白(CFP)的方法。该方法采用LKB Multiphor对全血清进行电聚焦,而不是先前研究中使用的仪器。需要进行两项基本改进:(1)使用pH 2.5 - 10.0的梯度代替pH 5 - 10的梯度,(2)对血清蛋白聚焦采用恒功率而不是恒电压。第一项改进确保了CFP - IgG复合物(或其他可能释放CFP的前体复合物)的充分溶解。第二项改进确保了线性梯度(在pH 3.8和pH 9.2之间),在pH 8 - 9区域具有出色的分辨率,并且能在2小时内分离出CFP,同时凝胶不会过热。使用LKB Multiphor进行电聚焦,每块凝胶可检测多达24份血清样本中的CFP。对31份囊性纤维化患者血清、28份必然杂合子携带者血清和28份正常对照血清的分析结果表明,使用LKB Multiphor可在血清中可重复且准确地检测到CFP。