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EXPISFand#8482;: A chemically-defined baculovirus-based expressio | 58841
Journal of Clinical and Cellular Immunology

Journal of Clinical and Cellular Immunology
Open Access

ISSN: 2155-9899

+44 1223 790975

EXPISF™: A chemically-defined baculovirus-based expression system for vaccine production in Sf9 cells


Joint Event on 36th Euro Global Summit and Expo on Vaccines & Vaccination & 6th World Congress and Exhibition on Antibiotics and Antibiotic Resistance

June 03-04, 2019 London, UK

Natasha Lucki, Maya Yovcheva, Kenneth Thompson, Sara Barnes, Melissa Cross, Katy Irvin, Henry Chiou and Jonathan Zmuda

Thermo Fisher Scientific, Inc., USA

Scientific Tracks Abstracts: J Clin Cell Immunol

Abstract :

Baculovirus-insect cell expression system is one of the major platforms for recombinant protein production and a robust and versatile platform for vaccine production. Currently, eight commercially-available vaccine products and multiple vaccine candidates in development are produced in insect cells. Unlike mammalian expression systems that have long since transitioned to chemically defined culture media, relatively little innovation has taken place in insect expression systems. Insect cells continue to rely on undefined, yeastolate-containing culture media that can exhibit significant lot-to-lot performance variability and, therefore, negatively impact productivity. Here, we describe the ExpiSf�?� Expression System, the first chemically defined insect expression system that enables highyield production of proteins and viral particles with consistent performance run after run using a fast, streamlined workflow. This multi-component, optimized system delivers scalable yields from shake flask to bioreactor scale, thus facilitating vaccine development. The superior performance of ExpiSf provides researchers with the simplicity of obtaining high-titer recombinant baculovirus in one simple step and going from transfection to product harvest in 6-10 days.

Biography :

Natasha is a Product Manager at Thermo Fisher Scientific managing the insect and CHO protein expression product portfolios. Prior to joining Thermo Fisher, Natasha has completed postdoctoral research training in early-stage drug discovery at the California Institute for Biomedical Research in La Jolla, CA, USA and received a PhD in Cell & Molecular Biology from the Georgia Institute of Technology in Atlanta, GA, USA.

E-mail: natasha.lucki@thermofisher.com

 

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