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A full-genomic sequence-verified protein-coding gene collection for Francisella tularensis
Authors:Murthy Tal  Rolfs Andreas  Hu Yanhui  Shi Zhenwei  Raphael Jacob  Moreira Donna  Kelley Fontina  McCarron Seamus  Jepson Daniel  Taycher Elena  Zuo Dongmei  Mohr Stephanie E  Fernandez Mauricio  Brizuela Leonardo  LaBaer Joshua
Affiliation:Harvard Institute of Proteomics, Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Cambridge, Massachusetts, United States of America.
Abstract:The rapid development of new technologies for the high throughput (HT) study of proteins has increased the demand for comprehensive plasmid clone resources that support protein expression. These clones must be full-length, sequence-verified and in a flexible format. The generation of these resources requires automated pipelines supported by software management systems. Although the availability of clone resources is growing, current collections are either not complete or not fully sequence-verified. We report an automated pipeline, supported by several software applications that enabled the construction of the first comprehensive sequence-verified plasmid clone resource for more than 96% of protein coding sequences of the genome of F. tularensis, a highly virulent human pathogen and the causative agent of tularemia. This clone resource was applied to a HT protein purification pipeline successfully producing recombinant proteins for 72% of the genes. These methods and resources represent significant technological steps towards exploiting the genomic information of F. tularensis in discovery applications.
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