Element-tagged immunoassay with ICP-MS detection: Evaluation and comparison to conventional immunoassays

被引:51
|
作者
Razumienko, Eva [1 ]
Ornatsky, Olga [1 ]
Kinach, Robert [1 ]
Milyavsky, Michael [2 ]
Lechman, Eric [2 ]
Baranov, Vladimir [1 ]
Winnik, Mitchell A. [1 ]
Tanner, Scott D. [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
[2] Univ Hlth Network, Div Cellular & Mol Biol, Toronto, ON M5G2M9, Canada
关键词
ELISA; ICP-MS; element-tagged antibody; lanthanides; growth factors; transcription factor p53;
D O I
10.1016/j.jim.2008.03.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated the possibility of using element-tagged antibodies for protein detection and quantification in microplate format using Inductively Coupled Plasma Mass Spectrometry (ICP-MS), and compared the results to conventional immunoassays, such as Enzyme-Linked Immunosorbent Assay (ELISA) and Western blotting. The technique was further employed to detect low levels and measure DNA-binding activity of transcription factor p53 in leukemia cell lysates through its interaction with immobilized oligonucleotides and recognition by element-tagged antibodies. The advantages of ICP-MS detection for routine performance of immunoassays include increased sensitivity, wide dynamic range, minimal interference from complex matrices, and high throughput. Our approach advances the ICP-MS technology and demonstrates its applicability to proteomic studies through the use of antibodies directly labeled with polymer tags bearing multiple atoms of lanthanides. Development of this novel methodology will enable fast and quantitative identification of multiple analytes in a single well. Crown Copyright (C) 2008 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:56 / 63
页数:8
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