Protein microarrays: prospects and problems

被引:394
作者
Kodadek, T
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Ctr Biomed Invent, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Biochem, Ctr Biomed Invent, Dallas, TX 75390 USA
来源
CHEMISTRY & BIOLOGY | 2001年 / 8卷 / 02期
关键词
protein array; microarray; protein-protein interaction; protein immobilization; surface plasmon resonance;
D O I
10.1016/S1074-5521(00)90067-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein microarrays are potentially powerful tools in biochemistry and molecular biology. Two types of protein microarrays are defined. One, termed a protein function array, will consist of thousands of native proteins immobilized in a defined pattern. Such arrays can be utilized for massively parallel testing of protein function, hence the name. The other type is termed a protein-detecting array. This will consist of large numbers of arrayed protein-binding agents. These arrays will allow for expression profiling to be done at the protein level. In this article, some of the major technological challenges to the development of protein arrays are discussed, along with potential solutions. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:105 / 115
页数:11
相关论文
共 39 条
[31]   Proteomics to study genes and genomes [J].
Pandey, A ;
Mann, M .
NATURE, 2000, 405 (6788) :837-846
[32]   PROTEIN-PROTEIN INTERACTIONS - METHODS FOR DETECTION AND ANALYSIS [J].
PHIZICKY, EM ;
FIELDS, S .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :94-123
[33]   Phage display of combinatorial antibody libraries [J].
Rader, C ;
Barbas, CF .
CURRENT OPINION IN BIOTECHNOLOGY, 1997, 8 (04) :503-508
[34]   Advances in surface plasmon resonance biosensor analysis [J].
Rich, RL ;
Myszka, DG .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (01) :54-61
[35]   Discovering high-affinity ligands for proteins: SAR by NMR [J].
Shuker, SB ;
Hajduk, PJ ;
Meadows, RP ;
Fesik, SW .
SCIENCE, 1996, 274 (5292) :1531-1534
[36]   A versatile plasmid expression vector for the production of biotinylated proteins by site-specific, enzymatic modification in Escherichia coli [J].
Tsao, KL ;
DeBarbieri, B ;
Michel, H ;
Waugh, DS .
GENE, 1996, 169 (01) :59-64
[37]   SYSTEMATIC EVOLUTION OF LIGANDS BY EXPONENTIAL ENRICHMENT - RNA LIGANDS TO BACTERIOPHAGE-T4 DNA-POLYMERASE [J].
TUERK, C ;
GOLD, L .
SCIENCE, 1990, 249 (4968) :505-510
[38]   Selection and application of peptide-binding peptides [J].
Zhang, ZW ;
Zhu, WG ;
Kodadek, T .
NATURE BIOTECHNOLOGY, 2000, 18 (01) :71-74
[39]   A CDC6 protein-binding peptide selected using a bacterial two-hybrid-like system is a cell cycle inhibitor [J].
Zhu, WG ;
Williams, RS ;
Kodadek, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :32098-32105