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On the influence of vector design on antibody phage display.

On the influence of vector design on antibody phage display. Research Abstract Details 

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  • On the influence of vector design on antibody phage display. Abstract Text:

    glenn soltesGlenn Soltes,michael hustMichael Hust,kitty k y ngKitty K Y Ng,aasthaa bansalAasthaa Bansal,johnathan fieldJohnathan Field,donald i h stewartDonald I H Stewart,stefan Stefan ,sanghoon chaSanghoon Cha,erik j wiersmaErik J Wiersma,

    Phage display technology is an established technology particularly useful for the generation of monoclonal antibodies (mAbs). The isolation of phagemid-encoded mAb fragments depends on several features of a phage preparation. The aims of this study were to optimize phage display vectors, and to ascertain if different virion features can be optimized independently of each other. Comparisons were made between phagemid virions assembled by g3p-deficient helper phage, Hyperphage, Ex-phage or Phaberge, or corresponding g3p-sufficient helper phage, M13K07. All g3p-deficient helper phage provided a similar level of antibody display, significantly higher than that of M13K07. Hyperphage packaged virions at least 100-fold more efficiently than did Ex-phage or Phaberge. Phaberge's packaging efficiency improved by using a SupE strain. Different phagemids were also compared. Removal of a 56 base pair fragment from the promoter region resulted in increased display level and increased virion production. This critical fragment encodes a lacZ'-like peptide and is also present in other commonly used phagemids. Increasing display level did not show statistical correlation with phage production, phage infectivity or bacterial growth rate. However, phage production was positively correlated to phage infectivity. In summary, this study demonstrates simultaneously optimization of multiple and independent features of importance for phage selection.

    On the influence of vector design on antibody phage display. Publishing Authors By Initials

    g soltesG Soltes,m hustM Hust,kk ngKK Ng,a bansalA Bansal,j fieldJ Field,di stewartDI Stewart,s S ,s chaS Cha,ej wiersmaEJ Wiersma,

    For similar viruses: virion research abstracts see: viruses: virion research

    PUBMED ID PMID:

    MEDLINE DATE:

    On the influence of vector design on antibody phage display. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of biotechnology

    VOLUME: 127

    Page Numbers: 626-37

    Journal Abbreviation: J. Biotechnol.

    ISSN: 0168-1656

    DAY: 22

    MONTH: 09

    YEAR: 2006

    On the influence of vector design on antibody phage display. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8411927

    On the influence of vector design on antibody phage display. Keywords Mesh Terms:

    KEYWORDS: Virion

    MESH TERMS: genetics

    Chemical & Substance for Abstract: On the influence of vector design on antibody phage display. Information

    Substance Name: Peptide Library

    Registry Number: 0

    Grant and Affiliation Information for On the influence of vector design on antibody phage display.

    AFFILIATION: Cangene Corporation, 3403 American Drive, Mississauga, Ontario L4V 1T4, Canada.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

    AGENCY: United States NIAID

    GRANT: U01AI056383-1

    ACRONYM: AI

    MEDLINETA: J Biotechnol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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