Antibody microarrays: Current status and key technological advances

被引:80
作者
Wingren, Christer [1 ]
Borrebaeck, Carl A. K. [1 ]
机构
[1] Lund Univ, Dept Immunotechnol, SE-22184 Lund, Sweden
关键词
D O I
10.1089/omi.2006.10.411
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Antibody-based microarrays are among the novel classes of rapidly evolving proteomic technologies that holds great promise in biomedicine. Miniaturized microarrays (< 1 cm(2)) can be printed with thousands of individual antibodies carrying the desired specificities, and with biological sample (e.g., an entire proteome) added, virtually any specifically bound analytes can be detected. While consuming only minute amounts (<mu L scale) of reagents, ultra-sensitive assays (zeptomol range) can readily be performed in a highly multiplexed manner. The microarray patterns generated can then be transformed into proteomic maps, or detailed molecular fingerprints, revealing the composition of the proteome. Thus, protein expression profiling and global proteome analysis using this tool will offer new opportunities for drug target and biomarker discovery, disease diagnostics, and insights into disease biology. Adopting the antibody microarray technology platform, several biomedical applications, ranging from focused assays to proteome-scale analysis will be rapidly emerging in the coming years. This review will discuss the current status of the antibody microarray technology focusing on recent technological advances and key issues in the process of evolving the methodology into a high-performing proteomic research tool.
引用
收藏
页码:411 / 427
页数:17
相关论文
共 131 条
[1]   Toward a human blood serum proteome - Analysis by multidimensional separation coupled with mass spectrometry [J].
Adkins, JN ;
Varnum, SM ;
Auberry, KJ ;
Moore, RJ ;
Angell, NH ;
Smith, RD ;
Springer, DL ;
Pounds, JG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (12) :947-955
[2]   The human plasma proteome - A nonredundant list developed by combination of four separate sources [J].
Anderson, NL ;
Polanski, M ;
Pieper, R ;
Gatlin, T ;
Tirumalai, RS ;
Conrads, TP ;
Veenstra, TD ;
Adkins, JN ;
Pounds, JG ;
Fagan, R ;
Lobley, A .
MOLECULAR & CELLULAR PROTEOMICS, 2004, 3 (04) :311-326
[3]   Subnanoliter enzymatic assays on microarrays [J].
Angenendt, P ;
Lehrach, H ;
Kreutzberger, J ;
Glökler, J .
PROTEOMICS, 2005, 5 (02) :420-425
[4]   Seeing better through a MIST: Evaluation of monoclonal recombinant antibody fragments on microarrays [J].
Angenendt, P ;
Wilde, J ;
Kijanka, G ;
Baars, S ;
Cahill, DJ ;
Kreutzberger, J ;
Lehrach, H ;
Konthur, Z ;
Glokler, J .
ANALYTICAL CHEMISTRY, 2004, 76 (10) :2916-2921
[5]   Cell-free protein expression and functional assay in nanowell chip format [J].
Angenendt, P ;
Nyarsik, L ;
Szaflarski, W ;
Glokler, J ;
Nierhaus, KH ;
Lehrach, H ;
Cahill, DJ ;
Lueking, A .
ANALYTICAL CHEMISTRY, 2004, 76 (07) :1844-1849
[6]   Next generation of protein microarray support materials:: Evaluation for protein and antibody microarray applications [J].
Angenendt, P ;
Glökler, J ;
Sobek, J ;
Lehrach, H ;
Cahill, DJ .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1009 (1-2) :97-104
[7]   Toward optimized antibody microarrays:: a comparison of current microarray support materials [J].
Angenendt, P ;
Glökler, J ;
Murphy, D ;
Lehrach, H ;
Cahill, DJ .
ANALYTICAL BIOCHEMISTRY, 2002, 309 (02) :253-260
[8]  
[Anonymous], 2005, NANOBIOTECHNOLOGY
[9]   Label-free protein assay based on a nanomechanical cantilever array [J].
Arntz, Y ;
Seelig, JD ;
Lang, HP ;
Zhang, J ;
Hunziker, P ;
Ramseyer, JP ;
Meyer, E ;
Hegner, M ;
Gerber, C .
NANOTECHNOLOGY, 2003, 14 (01) :86-90
[10]   A label-free immunosensor array using single-chain antibody fragments [J].
Backmann, N ;
Zahnd, C ;
Huber, F ;
Bietsch, A ;
Plückthun, A ;
Lang, HP ;
Güntherodt, HJ ;
Hegner, M ;
Gerber, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (41) :14587-14592