Chatterjee Deb K, Sitaraman Kalavathy, Baptista Cassio, Hartley James, Hill Thomas M, Munroe David J
Protein Expression Laboratory, SAIC-Frederick, Inc., NCI-Frederick, Frederick, Maryland, USA.
PLoS One. 2008 Sep 24;3(9):e3265. doi: 10.1371/journal.pone.0003265.
We describe a novel, simple and low-cost protein microarray strategy wherein the microarrays are generated by printing expression ready plasmid DNAs onto slides that can be converted into protein arrays on-demand. The printed expression plasmids serve dual purposes as they not only direct the synthesis of the protein of interest; they also serve to capture the newly synthesized proteins through a high affinity DNA-protein interaction. To accomplish this we have exploited the high-affinity binding (approximately 3-7 x 10 (-13) M) of E. coli Tus protein to Ter, a 20 bp DNA sequence involved in the regulation of E. coli DNA replication. In our system, each protein of interest is synthesized as a Tus fusion protein and each expression construct directing the protein synthesis contains embedded Ter DNA sequence. The embedded Ter sequence functions as a capture reagent for the newly synthesized Tus fusion protein. This "all DNA" microarray can be converted to a protein microarray on-demand without need for any additional capture reagent.
我们描述了一种新颖、简单且低成本的蛋白质微阵列策略,其中通过将表达就绪的质粒DNA打印到玻片上来生成微阵列,这些玻片可根据需要转化为蛋白质阵列。打印的表达质粒具有双重作用,它们不仅指导目标蛋白质的合成;还通过高亲和力的DNA-蛋白质相互作用捕获新合成的蛋白质。为实现这一点,我们利用了大肠杆菌Tus蛋白与Ter(一种参与大肠杆菌DNA复制调控的20bp DNA序列)之间的高亲和力结合(约3-7×10(-13)M)。在我们的系统中,每个目标蛋白质都作为Tus融合蛋白合成,并且每个指导蛋白质合成的表达构建体都包含嵌入的Ter DNA序列。嵌入的Ter序列作为新合成的Tus融合蛋白的捕获试剂。这种“全DNA”微阵列可根据需要转化为蛋白质微阵列,无需任何额外的捕获试剂。