Abstract
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 (∼3-7×10 -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. cr 2008 Chatterjee et al.
Cite
CITATION STYLE
Chatterjee, D. K., Sitaraman, K., Baptista, C., Hartley, J., Hill, T. M., & Munroe, D. J. (2008). Protein microarray on-demand: A novel protein microarray system. PLoS ONE, 3(9). https://doi.org/10.1371/journal.pone.0003265
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