Literature DB >> 7823859

SV40 virus expression vectors.

H Y Naim1, M G Roth.   

Abstract

SV40 late-replacement vectors provide an excellent means for expressing large amounts of proteins from cDNAs of less than 2400 bp. The amount of protein made 28 hr after infection is sufficient for extremely brief pulse-chase protocols. At periods postinfection when cells are still healthy, sufficient protein has been made for techniques in which only a small fraction of the protein is detected, including immunocytochemistry on cryosections. Because of the ease of subcloning DNA fragments into them, the ease of making virus stocks, and the ability to achieve comparable amounts of protein expression reproducibly with different infections, these vectors are superb tools for comparing series of mutants made by site-directed mutagenesis, especially if a normal cellular environment is important for the measurements to be made.

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Year:  1994        PMID: 7823859     DOI: 10.1016/s0091-679x(08)60601-9

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  7 in total

1.  Evolution of intermediates of influenza virus hemagglutinin-mediated fusion revealed by kinetic measurements of pore formation.

Authors:  R M Markosyan; G B Melikyan; F S Cohen
Journal:  Biophys J       Date:  2001-02       Impact factor: 4.033

2.  A point mutation in the transmembrane domain of the hemagglutinin of influenza virus stabilizes a hemifusion intermediate that can transit to fusion.

Authors:  G B Melikyan; R M Markosyan; M G Roth; F S Cohen
Journal:  Mol Biol Cell       Date:  2000-11       Impact factor: 4.138

3.  Amino acid sequence requirements of the transmembrane and cytoplasmic domains of influenza virus hemagglutinin for viable membrane fusion.

Authors:  G B Melikyan; S Lin; M G Roth; F S Cohen
Journal:  Mol Biol Cell       Date:  1999-06       Impact factor: 4.138

4.  Measles virus matrix protein specifies apical virus release and glycoprotein sorting in epithelial cells.

Authors:  H Y Naim; E Ehler; M A Billeter
Journal:  EMBO J       Date:  2000-07-17       Impact factor: 11.598

5.  Cell surface expression of biologically active influenza C virus HEF glycoprotein expressed from cDNA.

Authors:  A Pekosz; R A Lamb
Journal:  J Virol       Date:  1999-10       Impact factor: 5.103

6.  Bcl-2 inhibits apoptosis and extends recombinant protein production in cells infected with Sindbis viral vectors.

Authors:  A J Mastrangelo; J M Hardwick; M J Betenbaugh
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

7.  Endocytosis of chimeric influenza virus hemagglutinin proteins that lack a cytoplasmic recognition feature for coated pits.

Authors:  J Lazarovits; H Y Naim; A C Rodriguez; R H Wang; E Fire; C Bird; Y I Henis; M G Roth
Journal:  J Cell Biol       Date:  1996-07       Impact factor: 10.539

  7 in total

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