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  1. Article: The transient expression of CHIKV VLP in large stirred tank bioreactors.

    Chen, Peifeng / Demirji, Jacob / Ivleva, Vera B / Horwitz, Joe / Schwartz, Richard / Arnold, Frank

    Cytotechnology

    2019  Volume 71, Issue 6, Page(s) 1079–1093

    Abstract: Transient gene expression (TGE) bioprocesses have been difficult to scale up in large stirred tank bioreactors with volumes of more than 1.5 L. Low production levels are often observed, but the causes have not been investigated (Gutierrez-Granados et al. ...

    Abstract Transient gene expression (TGE) bioprocesses have been difficult to scale up in large stirred tank bioreactors with volumes of more than 1.5 L. Low production levels are often observed, but the causes have not been investigated (Gutierrez-Granados et al. in Crit Rev Biotechnol 38:918-940, 2018). Chikungunya Virus-like particle (VLP), expressed by DNA-PEI transient transfection, is a representative case study for these difficulties. Clinical materials were produced in shake flasks, but the process suffered when transferred to large stirred tank bioreactors. The resulting process was not operationally friendly nor cost effective. In this study, a systematic approach was used to investigate the root causes of the poor scale up performance. The transfection conditions were first screened in ambr® 15 high throughput mini bioreactors then examined in 3 L stirred-tank systems. The studies found that production level was negatively correlated with inoculum cell growth status (P < 0.05). The pH range, DNA and PEI levels, order of the reagent addition, and gas-sparging systems were also studied and found to affect process performance. Further hydromechanical characterizations (Re, energy dissipation rates, and P/V, etc.) of shake flasks, ambr® 15, and 3-L stirred tank systems were performed. Overall, the study discovered that the shear stress (caused by a microsparger) and PEI toxicity together were the root causes of scale-up failure. Once the microsparger was replaced by a macrosparger, the scale-up was successful.
    Language English
    Publishing date 2019-09-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1035772-5
    ISSN 0920-9069
    ISSN 0920-9069
    DOI 10.1007/s10616-019-00346-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Development of an alternating tangential flow (ATF) perfusion-based transient gene expression (TGE) bioprocess for universal influenza vaccine.

    Hong, Jinsung / Demirji, Jacob / Blackstock, Daniel / Lee, James / Dinh, Tracey / Goh, Alvenne / Arnold, Frank / Horwitz, Joe

    Biotechnology progress

    2019  Volume 35, Issue 5, Page(s) e2831

    Abstract: An alternating tangential flow (ATF) perfusion-based transient gene expression (TGE) bioprocess has been developed using human embryonic kidney (HEK) 293 cells to produce H1-ss-np, a promising candidate for a universal influenza vaccine. Two major ... ...

    Abstract An alternating tangential flow (ATF) perfusion-based transient gene expression (TGE) bioprocess has been developed using human embryonic kidney (HEK) 293 cells to produce H1-ss-np, a promising candidate for a universal influenza vaccine. Two major adjustments were taken to improve the process: (1) eliminate the interference of microbubbles during gene transfection; and (2) utilize an ATF perfusion system for a prolonged culture period. As a result, a closed-operation 9-days ATF perfusion-based TGE bioprocess was developed. The TGE bioprocess showed continuous cell growth with high cell viability and prolonged cellular productivity that achieved recombinant product level of ~270 mg/L which was more than two times that of 4-days base-line TGE bioprocess. In addition, the consumables cost per milligram for ATF perfusion-based TGE bioprocess was ~70% lower than that of the base-line TGE bioprocess suggesting high cost savings potential in vaccine manufacturing. Based on the lower contamination risk, higher productivity, and cost efficiency, the ATF perfusion-based TGE bioprocess can likely provide potential benefits to many future applications in vaccine and drug manufacturing.
    MeSH term(s) Bioreactors ; Cell Count ; Cell Culture Techniques/methods ; Cell Survival/physiology ; Gene Expression ; HEK293 Cells ; Humans ; Influenza Vaccines/chemistry ; Influenza Vaccines/genetics ; Influenza Vaccines/metabolism ; Nanoparticles ; Recombinant Proteins/chemistry ; Recombinant Proteins/genetics ; Recombinant Proteins/metabolism
    Chemical Substances Influenza Vaccines ; Recombinant Proteins
    Language English
    Publishing date 2019-05-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 165657-0
    ISSN 1520-6033 ; 8756-7938
    ISSN (online) 1520-6033
    ISSN 8756-7938
    DOI 10.1002/btpr.2831
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Tyrosine O-sulfation proteoforms affect HIV-1 monoclonal antibody potency.

    Cai, Cindy X / Doria-Rose, Nicole A / Schneck, Nicole A / Ivleva, Vera B / Tippett, Brad / Shadrick, William R / O'Connell, Sarah / Cooper, Jonathan W / Schneiderman, Zachary / Zhang, Baoshan / Gowetski, Daniel B / Blackstock, Daniel / Demirji, Jacob / Lin, Bob C / Gorman, Jason / Liu, Tracy / Li, Yile / McDermott, Adrian B / Kwong, Peter D /
    Carlton, Kevin / Gall, Jason G / Lei, Q Paula

    Scientific reports

    2022  Volume 12, Issue 1, Page(s) 8433

    Abstract: CAP256V2LS, a broadly neutralizing monoclonal antibody (bNAb), is being pursued as a promising drug for HIV-1 prevention. The total level of tyrosine-O-sulfation, a post-translational modification, was known to play a key role for antibody biological ... ...

    Abstract CAP256V2LS, a broadly neutralizing monoclonal antibody (bNAb), is being pursued as a promising drug for HIV-1 prevention. The total level of tyrosine-O-sulfation, a post-translational modification, was known to play a key role for antibody biological activity. More importantly, here wedescribe for the first time the significance of the tyrosine-O-sulfation proteoforms. We developed a hydrophobic interaction chromatography (HIC) method to separate and quantify different sulfation proteoforms, which led to the direct functionality assessment of tyrosine-sulfated species. The fully sulfated (4-SO
    MeSH term(s) Animals ; Antibodies, Monoclonal/pharmacology ; Antibodies, Neutralizing ; Broadly Neutralizing Antibodies ; CHO Cells ; Cricetinae ; HIV Antibodies ; HIV-1 ; Tyrosine/chemistry
    Chemical Substances Antibodies, Monoclonal ; Antibodies, Neutralizing ; Broadly Neutralizing Antibodies ; HIV Antibodies ; Tyrosine (42HK56048U)
    Language English
    Publishing date 2022-05-19
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-022-12423-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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