Title of article
Protein microarray technology
Author/Authors
Markus F Templin، نويسنده , , Rolf Dieter Stoll، نويسنده , , Monika Schrenk، نويسنده , , Petra C Traub، نويسنده , , Christian F V?hringer، نويسنده , , Thomas O Joos، نويسنده ,
Issue Information
ماهنامه با شماره پیاپی سال 2002
Pages
7
From page
160
To page
166
Abstract
Microarray technology allows the simultaneous analysis of thousands of parameters within a single experiment. Microspots of capture molecules are immobilized in rows and columns onto a solid support and exposed to samples containing the corresponding binding molecules. Readout systems based on fluorescence, chemiluminescence, mass spectrometry, radioactivity or electrochemistry can be used to detect complex formation within each microspot. Such miniaturized and parallelized binding assays can be highly sensitive, and the extraordinary power of the method is exemplified by array-based gene expression analysis. In these systems, arrays containing immobilized DNA probes are exposed to complementary targets and the degree of hybridization is measured. Recent developments in the field of protein microarrays show applications for enzyme–substrate, DNA–protein and different types of protein–protein interactions. Here, we discuss theoretical advantages and limitations of any miniaturized capture-molecule–ligand assay system and discusses how the use of protein microarrays will change diagnostic methods and genome and proteome research.
Keywords
Microarrays , cluorescence , Chemiluminescence , capture-molucule-ligand assay system , enzyme-substrate , DNA-protein , microspots
Journal title
Trends in Biotechnology
Serial Year
2002
Journal title
Trends in Biotechnology
Record number
1232722
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