Stoll Dieter, Templin Markus F, Schrenk Monika, Traub Petra C, Vöhringer Christian F, Joos Thomas O
NMI Natural and Medical Sciences Institute at the University of Tuebingen, Markwiesenstr. 55, 72770 Reutlingen, Germany.
Front Biosci. 2002 Jan 1;7:c13-32. doi: 10.2741/stoll.
This review summarizes the major activities in the field of protein microarray technology. A short summary of the theoretical concepts of miniaturized ligand binding assays explains why such microspot assays represent the most sensitive approaches for capture-target assays. The main focus of this review is centered on the applications using miniaturized and parallelized protein binding assays which rely on the product formation between immobilized capture molecules and their corresponding target molecules which are present in the sample. These types of ligand binding assays are useful tools for protein identification, quantification and protein affinity studies. Protein identification and quantification assays have a great potential in the field of diagnostics and proteomics where many different protein markers which are present in complex samples have to be analyzed in parallel. Protein affinity assays can be used to analyze interactions between proteins such as antibodies, receptors or enzymes with other proteins, peptides, low molecular weight compounds, oligosaccharides or DNA. Different applications of protein microarray-based assays and their huge potential for diagnostic and proteomic approaches will be discussed.
本综述总结了蛋白质微阵列技术领域的主要活动。对小型化配体结合测定的理论概念进行了简要概述,解释了为何此类微斑点测定是捕获 - 靶标测定中最灵敏的方法。本综述的主要重点集中在使用小型化和平行化蛋白质结合测定的应用上,这些测定依赖于固定化捕获分子与其样品中存在的相应靶标分子之间的产物形成。这些类型的配体结合测定是蛋白质鉴定、定量和蛋白质亲和力研究的有用工具。蛋白质鉴定和定量测定在诊断和蛋白质组学领域具有巨大潜力,在这些领域中,必须并行分析复杂样品中存在的许多不同蛋白质标志物。蛋白质亲和力测定可用于分析蛋白质(如抗体、受体或酶)与其他蛋白质、肽、低分子量化合物、寡糖或DNA之间的相互作用。将讨论基于蛋白质微阵列测定的不同应用及其在诊断和蛋白质组学方法中的巨大潜力。