Field Simon, Udalova Irina, Ragoussis Jiannis
Wellcome Trust Centre for Human Genetics, University of Oxford, 7 Roosevelt Drive, Oxford OX3 7BN, UK.
Adv Biochem Eng Biotechnol. 2007;104:87-110. doi: 10.1007/10_2006_035.
Microarray-based methods for understanding protein-DNA interactions have been developed in the last 6 years due to the need to introduce high-throughput technologies in this field. Protein-DNA microarrays utilise chips upon which a large number of DNA sequences may be printed or synthesised. Any DNA-binding protein may then be interrogated by applying either purified sample or cellular/nuclear extracts, subject to availability of a suitable detection system. Protein is simply added to the microarray slide surface, which is then washed and subjected to at least one further incubation with a labelled molecule which binds specifically to the protein of interest. The signal obtained is proportional to the level of DNA-binding protein bound to each DNA feature, enabling relative affinities to be calculated. Key factors for reproducible and accurate quantification of protein binding are: microarray surface chemistry; length of oligonucleotides; position of the binding site sequence; quality of the protein and antibodies; and hybridisation conditions.
由于需要在该领域引入高通量技术,基于微阵列的用于理解蛋白质 - DNA相互作用的方法在过去6年中得到了发展。蛋白质 - DNA微阵列利用芯片,在其上可以印刷或合成大量DNA序列。然后,通过应用纯化样品或细胞/核提取物来检测任何DNA结合蛋白,前提是有合适的检测系统。只需将蛋白质添加到微阵列载玻片表面,然后洗涤,再与特异性结合目标蛋白质的标记分子进行至少一次进一步孵育。获得的信号与结合到每个DNA特征的DNA结合蛋白水平成比例,从而能够计算相对亲和力。蛋白质结合的可重复和准确定量的关键因素包括:微阵列表面化学;寡核苷酸长度;结合位点序列的位置;蛋白质和抗体的质量;以及杂交条件。