Protein micro- and macroarrays: digitizing the proteome

被引:43
作者
Lopez, MF [1 ]
Pluskal, MG [1 ]
机构
[1] Proteome Syst, Woburn, MA 01801 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2003年 / 787卷 / 01期
关键词
reviews; microassays; macroassays; proteins; proteomes;
D O I
10.1016/S1570-0232(02)00336-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The early applications of microarrays and detection technologies have been centered on DNA-based applications. The application of array technologies to proteomics is now occurring at a rapid rate. Numerous researchers have begun to develop technologies for the creation of microarrays of protein-based screening tools. The stability of antibody molecules when bound to surfaces has made antibody arrays a starting point for proteomic microarray technology. To minimize disadvantages due to size and availability, some researchers have instead opted for antibody fragments, antibody mimics or phage display technology to create libraries for protein chips. Even further removed from antibodies are libraries of aptamers, which are single-stranded oligonucleotides that express high affinity for protein molecules. A variation on the theme of protein chips arrayed with antibody mimics or other protein capture ligand is that of affinity MS where the protein chips are directly placed in a mass spectrometer for detection. Other approaches include the creation of intact protein microarrays directly on glass slides or chips. Although many of the proteins may likely be denatured, successful screening has been demonstrated. The investigation of protein-protein interactions has formed the basis of a technique called yeast two-hybrid. In this method, yeast "bait" proteins can be probed with other yeast "prey" proteins fused to DNA binding domains. Although the current interpretation of protein arrays emphasizes microarray grids of proteins or ligands on glass slides or chips, 2-D gels are technically macroarrays of authentic proteins. In an innovative departure from the traditional concept of protein chips, some researchers are implementing microfluidic printing of arrayed chemistries on individual protein spots blotted onto membranes. Other researchers are using in-jet printing technology to create protein microarrays on chips. The rapid growth of proteomics and the active climate for new technology is driving a new generation of companies and academic efforts that are developing novel protein microarray techniques for the future. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:19 / 27
页数:9
相关论文
共 75 条
[21]   THE CURRENT STATE OF TWO-DIMENSIONAL ELECTROPHORESIS WITH IMMOBILIZED PH GRADIENTS [J].
GORG, A ;
POSTEL, W ;
GUNTHER, S .
ELECTROPHORESIS, 1988, 9 (09) :531-546
[22]  
Haab B B, 2001, Curr Opin Drug Discov Devel, V4, P116
[23]  
Haab BB, 2001, GENOME BIOL, V2
[24]   HIGHLY RESOLVING 2-DIMENSIONAL GELS FOR PROTEIN SEQUENCING [J].
HANASH, SM ;
STRAHLER, JR ;
NEEL, JV ;
HAILAT, N ;
MELHEM, R ;
KEIM, D ;
ZHU, XX ;
WAGNER, D ;
GAGE, DA ;
WATSON, JT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (13) :5709-5713
[25]   Probing the proteome - protein arrays and their applications [J].
Hayward, RE ;
Cameron, G ;
Kozlowski, RZ .
DRUG DISCOVERY TODAY, 2001, 6 (24) :1263-1265
[26]   What place for polyacrylamide in proteomics? [J].
Herbert, BR ;
Harry, JL ;
Packer, NH ;
Gooley, AA ;
Pedersen, SK ;
Williams, KL .
TRENDS IN BIOTECHNOLOGY, 2001, 19 (10) :S3-S9
[27]   Biochemistry - Adaptive recognition by nucleic acid aptamers [J].
Hermann, T ;
Patel, DJ .
SCIENCE, 2000, 287 (5454) :820-825
[28]  
Igloi G L, 1996, Methods Mol Biol, V65, P23
[29]   Toward a protein-protein interaction map of the budding yeast: A comprehensive system to examine two-hybrid interactions in all possible combinations between the yeast proteins [J].
Ito, T ;
Tashiro, K ;
Muta, S ;
Ozawa, R ;
Chiba, T ;
Nishizawa, M ;
Yamamoto, K ;
Kuhara, S ;
Sakaki, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (03) :1143-1147
[30]  
Jenkins RE, 2001, PROTEOMICS, V1, P13, DOI 10.1002/1615-9861(200101)1:1<13::AID-PROT13>3.3.CO