A very sensitive coupled luminescent assay for cytotoxicity and complement-mediated lysis

被引:37
作者
Corey, MJ [1 ]
Kinders, RJ [1 ]
Brown, LG [1 ]
Vessella, RL [1 ]
机构
[1] BARD DIAGNOST SCI INC,REDMOND,WA 98052
关键词
factor H; glyceraldehyde-3-phosphate dehydrogenase; ATP; membrane damage; enzyme release;
D O I
10.1016/S0022-1759(97)00098-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The demand for convenient and sensitive means of measuring cytotoxicity and complement-mediated killing is likely to be increased by the recent identification of Complement Factor H, an important regulatory protein of both the classical and alternate pathways of complement, as a tumor-associated antigen. Here we describe a simple luminometric assay capable of detecting the death of similar to 0.03 nucleated human-cell equivalent or similar to 1 rabbit-erythrocyte equivalent. The assay measures the release of glyceraldehyde-3-phosphate dehydrogenase (G3PDH) from dead or damaged cells by coupling its enzymatic activity to production of ATP, which in turn is measured by well-known methods involving firefly luciferase. This is accomplished by means of a reaction series in which the activity of G3PDH is coupled with that of phosphoglycerate kinase, the next enzyme in the glycolytic pathway. As described, the assay uses inexpensive, commercially available reagents. This coupled assay was used to demonstrate that an anti-factor-H antibody is capable of enhancing complement-mediated killing of the Raji cancer cell line by > 1000%. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:43 / 51
页数:9
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