Schlosser Gitta, Pocsfalvi Gabriella, Malorni Antonio, Puerta Angel, de Frutos Mercedes, Vékey Károly
Chemical Research Center, Hungarian Academy of Sciences, Budapest, Hungary.
Rapid Commun Mass Spectrom. 2003;17(24):2741-7. doi: 10.1002/rcm.1239.
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) was used to detect an immune complex formed between beta-lactoglobulin and polyclonal anti-beta-lactoglobulin antibody in the gas phase. The most important experimental parameters to detect such a specific antibody-antigen complex by MALDI were the use of solutions at near-neutral pH and of sinapinic acid matrix prepared by the dried-droplet method. Under such conditions, predominantly one but also two molecules of antigen protein were complexed by the antibody. Specific formation of the antibody-antigen complex was confirmed by performing competitive reactions. Addition of antibody to a 1:1 mixture of beta-lactoglobulin and one control protein resulted not only in the appearance of the expected antibody-antigen complex, but also in a strong decrease in the free beta-lactoglobulin signal, while the abundance of the control protein was not influenced.
基质辅助激光解吸/电离质谱法(MALDI-MS)用于检测气相中β-乳球蛋白与多克隆抗β-乳球蛋白抗体形成的免疫复合物。通过MALDI检测这种特异性抗体-抗原复合物的最重要实验参数是使用近中性pH的溶液和通过干滴法制备的芥子酸基质。在这种条件下,抗体主要与一分子抗原蛋白结合,但也会与两分子抗原蛋白结合。通过进行竞争反应证实了抗体-抗原复合物的特异性形成。将抗体添加到β-乳球蛋白与一种对照蛋白的1:1混合物中,不仅导致预期的抗体-抗原复合物出现,还导致游离β-乳球蛋白信号大幅下降,而对照蛋白的丰度不受影响。