Development of a high-throughput plate-based chemiluminescent transcription factor assay

被引:31
作者
Rosenau, C [1 ]
Emery, D [1 ]
Kaboord, B [1 ]
Qoronfleh, MW [1 ]
机构
[1] Pierce Biotechnol Inc, Perbio Sci Biores Div, Milwaukee, WI 53202 USA
关键词
transcription factors; chemiluminescence; electrophoretic mobility shift assay (EMSA); nuclear factor kappa B (NF kappa B); activator protein-1 (AP-1); DNA-binding proteins; gel shift assay;
D O I
10.1177/1087057103261446
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transcription factors are DNA-binding proteins that regulate the expression of specific genes by controlling transcription initiation. Two families of transcription factors, NFkappaB and AP-1, play pivotal roles in controlling important cellular processes ranging from normal cell growth and differentiation to apoptosis and cancer. Identifying changes in the DNA-binding activity of these factors is essential to understanding the regulation of these processes. We have developed a high-throughput DNA-based ELISA capable of monitoring activated levels of NFkappaB (p50 and p65) and AP-1 (c-Jun and c-Fos). This chemiluminescent assay utilizes a 96-well plate format, eliminating the throughput challenges imposed by traditional gel shift assays and exceeding the sensitivity and dynamic range of standard colorimetric detection systems. The sensitivity of this assay enables distinction between subtle as well as dramatic differences in the DNA-binding activity of these factors that result from the treatment of cells with various inhibitors or activating agents.
引用
收藏
页码:334 / 342
页数:9
相关论文
共 37 条
[1]  
Adcock I M, 1997, Monaldi Arch Chest Dis, V52, P178
[2]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[3]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[4]   Nonisotopic quantitative analysis of protein-DNA interactions at equilibrium [J].
Benotmane, AM ;
Hoylaerts, MF ;
Collen, D ;
Belayew, A .
ANALYTICAL BIOCHEMISTRY, 1997, 250 (02) :181-185
[5]   Inhibition of nuclear factor κB by direct modification in whole cells -: Mechanism of action of nordihydroguaiaritic acid, curcumin and thiol modifiers [J].
Brennan, P ;
O'Neill, LAJ .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (07) :965-973
[6]   Vitamin C suppresses TNFα-induced NFκB activation by inhibiting IκBα phosphorylation [J].
Cárcamo, JM ;
Pedraza, A ;
Bórquez-Ojeda, O ;
Golde, DW .
BIOCHEMISTRY, 2002, 41 (43) :12995-13002
[7]   JNK2 and IKKβ are required for activating the innate response to viral infection [J].
Chu, WM ;
Ostertag, D ;
Li, ZW ;
Chang, LF ;
Chen, Y ;
Hu, YL ;
Williams, B ;
Perrault, J ;
Karin, M .
IMMUNITY, 1999, 11 (06) :721-731
[8]   THE UV RESPONSE INVOLVING THE RAS SIGNALING PATHWAY AND AP-1 TRANSCRIPTION FACTORS IS CONSERVED BETWEEN YEAST AND MAMMALS [J].
ENGELBERG, D ;
KLEIN, C ;
MARTINETTO, H ;
STRUHL, K ;
KARIN, M .
CELL, 1994, 77 (03) :381-390
[9]  
Garg A, 2002, LEUKEMIA, V16, P1053, DOI 10.1038/sj.leu.2402482
[10]   Nordihydroguaiaretic acid-mediated inhibition of ultraviolet B-induced activator protein-1 activation in human keratinocytes [J].
Gonzales, M ;
Bowden, GT .
MOLECULAR CARCINOGENESIS, 2002, 34 (02) :102-111