NATX Plasmids, for: DNA Vaccines, Gene Therapeutics, Viral Vectors andBiophamacueticals

Vector, Strain, Process and Product Development

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Vector Development: From Concept to Reality

•     State of the art facilities

•     Expert staff

•     Rapid construction

•     Precision, single-base construction using GENSA technology


Vector development is the initial and rate limiting factor in biologics development

Without it, nothing happens; and with it, what happens is entirely dependent upon the planning and skill of the expert scientists and engineers in charge.  Vectors must reflect practical as well as IP considerations.  In many cases, NTC scientists start with time tested NTC vector systems that require only minor modifications, while in others, they use de novo-created parts that snap together like Legos, using NTC’s Gene Self-Assembly (GENSAtm) technology for seamless, ordered genetic surgery. In vitro or in vivo testing provides proof of concept and serves as the basis for final improvements, if any. [Case study: NTC’s pDNAVACCUltra DNA vaccination platform.]

Ref: Williams et al., 2009, Plasmid DNA vaccine vector design: Impact on efficacy, safety and upstream production
Carnes et al., Autolysis strains

Strain Development: Living Cell Factories for Biopharmaceutical Production

Specialized biological products require specialized cells or organisms for their production.  NTC has devised Genome Mass Transfer (GMTtm) technology for rapid, precise alteration of microbial genomes.  NTC’s bacterial host strains are made rapidly and precisely in response to the need for specialized genes, such as: autolytic genes for rapid processing; nucleases for clearance of host genomic DNA and RNA; or antisense RNAs for control over copy number or plasmid selection. [Case study: NTC’s autolytic processing host strains.]

Ref: Williams et al., 2009 Strain engineering by genome mass transfer: efficient chromosomal trait transfer method utilizing donor genomic DNA and recipient recombineering hosts







Process Development: Designing the Most Effective Methods of Production

BioProcess development represents the natural co-evolution of engineering and science, designed to produce complex biological molecules/entities, and purify them, typically in a two stage process: upstream (production in living cell factories); and downstream (purification).  Vectors and strains work together in the process, resulting in efficient, high-yield production and a highly purified product. Recombinant therapeutic proteins, vaccines, gene therapeutics, and monoclonal antibodies are some of the results. [Case study: NTC’s HyperGRO process for plasmid DNA fermentation.]

Ref: Carnes et al., 2009 Plasmid DNA production combining antibiotic-free selection, inducible high yield fermentation, and novel autolytic purification,



Fed-batch HyperGRO fermentation proces

 Fluorescent proteins in E. coli

Product Development: New Age Therapeutics Designed to Fit

Biopharmaceutical products are rationally designed drugs, specialized with precision to meet important biochemical and biophysical criteria and target specificity.  Bioproducts represent the sum total of efforts in concept, design, and execution. NTC scientists provide a success-driven roadmap for product development, aimed at later stage successes in the clinic and marketplace. [Case study: NTC’s fluorescent proteins for flow cytometry labeling.]



 

 

 

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