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通过基质辅助激光解吸/电离质谱法检测免疫复合物

Detection of immune complexes by matrix-assisted laser desorption/ionization mass spectrometry.

作者信息

Schlosser Gitta, Pocsfalvi Gabriella, Malorni Antonio, Puerta Angel, de Frutos Mercedes, Vékey Károly

机构信息

Chemical Research Center, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Rapid Commun Mass Spectrom. 2003;17(24):2741-7. doi: 10.1002/rcm.1239.

Abstract

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.

摘要

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。

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