Protein microarrays: a chance to study microorganisms?

被引:17
作者
Kreutzberger, J [1 ]
机构
[1] Max Planck Inst Mol Genet, Dept Lehrach, D-14195 Berlin, Germany
关键词
D O I
10.1007/s00253-006-0312-y
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
Within the last 5 years, protein microarrays have been developed and applied to multiple approaches: identification of protein-protein interactions or protein-small molecule interactions, cancer profiling, detection of microorganisms and toxins, and identification of antibodies due to allergens, autoantigens, and pathogens. Protein microarrays are small size (typically in the microscopy slide format) planar analytical devices with probes arranged in high density to provide the ability to screen several hundred to thousand known substrates (e.g., proteins, peptides, antibodies) simultaneously. Due to their small size, only minute amounts of spotted probes and analytes (e.g., serum) are needed; this is a particularly important feature, for these are limited or expensive. In this review, different types of protein microarrays are reviewed: protein microarrays (PMAs), with spotted proteins or peptides; antibody microarrays (AMAs), with spotted antibodies or antibody fragments (e.g., scFv); reverse phase protein microarrays (RPMAs), a special form of PMA where crude protein mixtures (e.g., cell lysates, fractions) are spotted; and nonprotein microarrays (NPMAs) where macromolecules other than proteins and nucleic acids (e.g., carbohydrates, monosaccharides, lipopolysaccharides) are spotted. In this study, exemplary experiments for all types of protein arrays are discussed wherever applicable with regard to investigations of microorganisms.
引用
收藏
页码:383 / 390
页数:8
相关论文
共 57 条
[1]   Subnanoliter enzymatic assays on microarrays [J].
Angenendt, P ;
Lehrach, H ;
Kreutzberger, J ;
Glökler, J .
PROTEOMICS, 2005, 5 (02) :420-425
[2]   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
[3]   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
[4]   3D protein microarrays:: Performing multiplex immunoassays on a single chip [J].
Angenendt, P ;
Glökler, J ;
Konthur, Z ;
Lehrach, H ;
Cahill, DJ .
ANALYTICAL CHEMISTRY, 2003, 75 (17) :4368-4372
[5]   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
[6]   A method for global protein expression and antibody screening on high-density filters of an arrayed cDNA library [J].
Büssow, K ;
Cahill, D ;
Nietfeld, W ;
Bancroft, D ;
Scherzinger, E ;
Lehrach, H ;
Walter, G .
NUCLEIC ACIDS RESEARCH, 1998, 26 (21) :5007-5008
[7]   Enzymatic activity on a chip: The critical role of protein orientation [J].
Cha, T ;
Guo, A ;
Zhu, XY .
PROTEOMICS, 2005, 5 (02) :416-419
[8]   Protein microarrays for multiplex analysis of signal transduction pathways [J].
Chan, SM ;
Ermann, J ;
Su, L ;
Fathman, CG ;
Utz, PJ .
NATURE MEDICINE, 2004, 10 (12) :1390-1396
[9]   Development of a protein microarray using sequence-specific DNA binding domain on DNA chip surface [J].
Choi, YS ;
Pack, SP ;
Yoo, YJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 329 (04) :1315-1319
[10]   A new polymeric coating for protein microarrays [J].
Cretich, M ;
Pirri, G ;
Damin, F ;
Solinas, I ;
Chiari, M .
ANALYTICAL BIOCHEMISTRY, 2004, 332 (01) :67-74