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Development of Arabidopsis Protein Chip
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| Summary: The genome sequence of Arabidopsis suggests that it contains approximately 30,700 protein-coding genes. A major goal of the 2010 program is to understand how each of these genes function during plant growth, development, and responses to biotic and abiotic cues. Global studies to analyze gene and protein function have largely focused on gene expression, gene disruption, protein interactions and protein localization. To elucidate biochemical activities of yeast proteome at the global scale, we have pioneered the development of protein chip technology. In our pilot project funded by NSF 2010 program, we have optimized high throughput techniques for cloning and expression of 1000 Arabidopsis ORFs to produce high quality active proteins for the generation of an Arabidopsis protein chip. In this project, we will generate a collection of expression clones that contain 4,000 predicted Arabidopsis ORFs as tandem affinity purification (TAP) tag fusions. We will express these proteins in the plant-based transient expression system to produce and purify proteins. The proteins will be printed on various printing surfaces to produce protein microarrays which will then be used to optimize protocols for analysis of protein activities. The reagents generated will be made available to the entire scientific community through our website. | ||
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Broader Impacts: Previously large scale genomics projects used protein localization,
protein-protein interactions, global gene expression profiles and knockouts to approximate the
function of the predicted gene products in Arabidopsis. Although informative, to truly elucidate
the function of gene products in a high throughput manner, new tools and techniques must be
developed to fully realize the potential of the sequenced genome. Therefore, the efforts we are
undertaking in this project will ultimately provide a valuable resource for a variety of
applications aimed at the high-throughput study of protein function in Arabidopsis. This project
will generate a suite of protocols specific to plant proteomes and generate a resourceful set of
plant expression clones and other reagents that are expected to significantly enhance the analysis
of protein function in Arabidopsis. Furthermore, the methods developed and information gained from
this study can also be directly applied to the analysis of other agriculturally and
horticulturally important plants. | ||