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Highly Efficient Purification of Recombinant VSV-∆G-Spike Vaccine against SARS-CoV-2 by Flow-Through Chromatography
by
Kafri, Yaron
, Cherry, Lilach
, Zichel, Ran
, Lupu, Edith
, Levy, Rona
, Natan, Niva
, Lerer, Elad
, Toister, Einat
, Monash, Arik
, Makovitzki, Arik
, Oren, Ziv
, Dor, Eyal
, Adar, Yaakov
, Girshengorn, Meni
, Levin, Lilach
, Epstein, Eyal
in
Anion-exchange chromatography
/ Cell culture
/ Chromatography
/ Coronaviruses
/ COVID-19
/ downstream process
/ Elution
/ Endonuclease
/ Glycoproteins
/ Infectivity
/ Influenza
/ Ion-exchange chromatography
/ membrane adsorbers
/ Molecular weight
/ Particle size
/ Proteins
/ Resins
/ rVSV
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Spike protein
/ Stomatitis
/ Surface area
/ Ultrafiltration
/ Vaccines
/ Vectors (Biology)
/ Viruses
2021
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Highly Efficient Purification of Recombinant VSV-∆G-Spike Vaccine against SARS-CoV-2 by Flow-Through Chromatography
by
Kafri, Yaron
, Cherry, Lilach
, Zichel, Ran
, Lupu, Edith
, Levy, Rona
, Natan, Niva
, Lerer, Elad
, Toister, Einat
, Monash, Arik
, Makovitzki, Arik
, Oren, Ziv
, Dor, Eyal
, Adar, Yaakov
, Girshengorn, Meni
, Levin, Lilach
, Epstein, Eyal
in
Anion-exchange chromatography
/ Cell culture
/ Chromatography
/ Coronaviruses
/ COVID-19
/ downstream process
/ Elution
/ Endonuclease
/ Glycoproteins
/ Infectivity
/ Influenza
/ Ion-exchange chromatography
/ membrane adsorbers
/ Molecular weight
/ Particle size
/ Proteins
/ Resins
/ rVSV
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Spike protein
/ Stomatitis
/ Surface area
/ Ultrafiltration
/ Vaccines
/ Vectors (Biology)
/ Viruses
2021
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Highly Efficient Purification of Recombinant VSV-∆G-Spike Vaccine against SARS-CoV-2 by Flow-Through Chromatography
by
Kafri, Yaron
, Cherry, Lilach
, Zichel, Ran
, Lupu, Edith
, Levy, Rona
, Natan, Niva
, Lerer, Elad
, Toister, Einat
, Monash, Arik
, Makovitzki, Arik
, Oren, Ziv
, Dor, Eyal
, Adar, Yaakov
, Girshengorn, Meni
, Levin, Lilach
, Epstein, Eyal
in
Anion-exchange chromatography
/ Cell culture
/ Chromatography
/ Coronaviruses
/ COVID-19
/ downstream process
/ Elution
/ Endonuclease
/ Glycoproteins
/ Infectivity
/ Influenza
/ Ion-exchange chromatography
/ membrane adsorbers
/ Molecular weight
/ Particle size
/ Proteins
/ Resins
/ rVSV
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Spike protein
/ Stomatitis
/ Surface area
/ Ultrafiltration
/ Vaccines
/ Vectors (Biology)
/ Viruses
2021
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Highly Efficient Purification of Recombinant VSV-∆G-Spike Vaccine against SARS-CoV-2 by Flow-Through Chromatography
Journal Article
Highly Efficient Purification of Recombinant VSV-∆G-Spike Vaccine against SARS-CoV-2 by Flow-Through Chromatography
2021
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Overview
This study reports a highly efficient, rapid one-step purification process for the production of the recombinant vesicular stomatitis virus-based vaccine, rVSV-∆G-spike (rVSV-S), recently developed by the Israel Institute for Biological Research (IIBR) for the prevention of COVID-19. Several purification strategies are evaluated using a variety of chromatography methods, including membrane adsorbers and packed-bed ion-exchange chromatography. Cell harvest is initially treated with endonuclease, clarified, and further concentrated by ultrafiltration before chromatography purification. The use of anion-exchange chromatography in all forms results in strong binding of the virus to the media, necessitating a high salt concentration for elution. The large virus and spike protein binds very strongly to the high surface area of the membrane adsorbents, resulting in poor virus recovery (<15%), while the use of packed-bed chromatography, where the surface area is smaller, achieves better recovery (up to 33%). Finally, a highly efficient chromatography purification process with CaptoTM Core 700 resin, which does not require binding and the elution of the virus, is described. rVSV-S cannot enter the inner pores of the resin and is collected in the flow-through eluent. Purification of the rVSV-S virus with CaptoTM Core 700 resulted in viral infectivity above 85% for this step, with the efficient removal of host cell proteins, consistent with regulatory requirements. Similar results were obtained without an initial ultrafiltration step.
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