Rehfeld J F
Dept. of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark.
Clin Chem. 1998 May;44(5):991-1001.
Shortage of reliable plasma assays has hampered studies of cholecystokinin (CCK). The assay problems are low plasma concentrations, extensive molecular heterogeneity, and close homology of CCK to gastrin, which circulates in higher concentrations. To develop an accurate CCK RIA, antibodies were raised in rabbits, guinea pigs, and mice in titers from 200 to 4000000. The specificity of the antisera was tested with homologous peptides, and tissue and plasma extracts. Rabbit 92128 produced antibodies in high titer (> or =500000) with sufficient avidity (K(o)eff > or = 10(12) mol(-1)) and the desired specificity. The antiserum binds the bioactive forms of CCK with equimolar potency and displays no reactivity with gastrin. CCK concentrations in plasma from healthy humans rose from 1.13 +/- 0.10 pmol/L (mean +/- SE, n = 26) to 4.92 +/- 0.34 pmol/L after a mixed meal. Chromatography of human plasma revealed traces of CCK-58, a predominance of CCK-33 and CCK-22, and moderate amounts of CCK-8. The results show that it is possible to produce specific CCK-antisera using a sulfated CCK-12 analog.
可靠的血浆检测方法的短缺阻碍了胆囊收缩素(CCK)的研究。检测问题包括血浆浓度低、分子异质性广泛以及CCK与胃泌素的高度同源性,而胃泌素以更高的浓度循环。为了开发一种准确的CCK放射免疫分析方法,在兔子、豚鼠和小鼠中产生了效价从200到4000000的抗体。用同源肽、组织和血浆提取物检测抗血清的特异性。兔子92128产生了高效价(≥500000)的抗体,具有足够的亲和力(K(o)eff≥10(12)mol(-1))和所需的特异性。该抗血清以等摩尔效力结合CCK的生物活性形式,并且与胃泌素无反应性。混合餐后,健康人血浆中的CCK浓度从1.13±0.10 pmol/L(平均值±标准误,n = 26)升至4.92±0.34 pmol/L。人血浆色谱分析显示有痕量的CCK-58、主要为CCK-33和CCK-22以及适量的CCK-8。结果表明,使用硫酸化的CCK-12类似物有可能产生特异性的CCK抗血清。