Design of high-density antibody microarrays for disease proteomics: Key technological issues

被引:96
作者
Borrebaeck, Carl A. K. [1 ,2 ]
Wingren, Christer [1 ,2 ]
机构
[1] Lund Univ, Dept Immunotechnol, SE-22184 Lund, Sweden
[2] Lund Univ, CREATE Hlth, SE-22184 Lund, Sweden
关键词
Antibody microarrays; Recombinant antibodies; Disease proteomics; Proteomics; Expression profiling; DNA-DIRECTED IMMOBILIZATION; DIP-PEN NANOLITHOGRAPHY; PROTEIN ARRAYS; CIRCULATING CYTOKINES; MASS-SPECTROMETRY; RECOMBINANT; EXPRESSION; GENERATION; QUANTIFICATION; IDENTIFICATION;
D O I
10.1016/j.jprot.2009.01.027
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody-based microarray is a novel proteomic technology setting a new standard for molecular profiling of non-fractionated complex proteomes. The first generation of antibody microarrays has already demonstrated its potential for generating detailed protein expression profiles, or protein atlases, of human body fluids in health and disease, paving the way for new discoveries within the field of disease proteomics. The process of designing highly miniaturized, high-density and high-performing antibody microarray set-ups have, however, proven to be challenging. in this mini-review we discuss key technological issues that must be addressed in a cross-disciplinary manner before true global proteome analysis can be performed using antibody microarrays. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:928 / 935
页数:8
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