Fully Automated Sample Processing and HTP ... - PerkinElmer

Fully Automated Sample Processing and HTP ... - PerkinElmer Fully Automated Sample Processing and HTP ... - PerkinElmer

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Pfēnex Expression Technology • P. fluorescens is a nonpathogenic, Gram-negative, obligate aerobic, bacterium • Genomic, “systems biology” approach to host strain construction enables rapid and reliable strain development • Combine expression plasmids for multiple expression strategies (promoter, ribosome binding site & secretion signal) with multiple host strains • Develop effective high throughput growth and assay methods • Rapid development of production strains yielding high titers of quality protein • Altered paradigm: Discard linear, iterative approach, adopt parallel, high throughput method for microbial strain development Discovery ● Development ● Production 4

Pfēnex HTP Strain Development >85% Success Rate for Proteins that Previously Failed in Other System Examples of Stalled Development: Protein Type Alternative Host Pfēnex Results Fab Yeast: quality issues, low yield 10-20X yield improvement high quality at 1L scale Microbial outer membrane protein E. coli: no expression Soluble active expression g/L; 1.0L scale Growth Factor Therapeutic Enzyme Human Cytokine Yeast: low yield, degradation, glycosylation E. coli: undesirable isoforms, quality issues E. coli- inclusion bodies; no soluble expression 20X yield improvement at HTP scale, high quality, active 10X yield improvement; no isoform issues Soluble active expression; elimination of refold step Multimeric Antibody Derivative CHO- low expression(

Pfēnex Expression Technology<br />

• P. fluorescens is a nonpathogenic, Gram-negative, obligate aerobic,<br />

bacterium<br />

• Genomic, “systems biology” approach to host strain construction enables<br />

rapid <strong>and</strong> reliable strain development<br />

• Combine expression plasmids for multiple expression strategies (promoter,<br />

ribosome binding site & secretion signal) with multiple host strains<br />

• Develop effective high throughput growth <strong>and</strong> assay methods<br />

• Rapid development of production strains yielding high titers of quality<br />

protein<br />

• Altered paradigm: Discard linear, iterative approach, adopt parallel, high<br />

throughput method for microbial strain development<br />

Discovery ● Development ● Production<br />

4

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