Production of high-titer human immunodeficiency virus type 1 pseudotyped with vesicular stomatitis virus glycoprotein

被引:132
作者
Bartz, SR
Vodicka, MA
机构
[1] Fred Hutchinson Cancer Res. Center, Seattle
[2] Division of Molecular Medicine, Fred Hutchinson Cancer Res. Center, Mailstop C2-023, Seattle, WA 98109-1024
来源
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY | 1997年 / 12卷 / 04期
关键词
D O I
10.1006/meth.1997.0487
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a method for the production of high-titer stocks of human immunodeficiency virus type 1 (HIV-1) pseudotyped with vesicular stomatitis virus envelope glycoprotein (VSV G). VSV G pseudotypes provide several advantages over other retroviral envelope proteins. The VSV G envelope is mechanically stable, enabling ultracentrifugal concentration of virions to high titers, and VSV G has a broad host range, enabling infection of many mammalian and nonmammalian cell types. VSV G pseudotypes of HIV-1 are useful for the study of HIV infection and replication kinetics and for the study of the function of specific viral proteins. We describe applications for the study of HIV-1 using VSV G pseudotypes. Additionally, we describe a method for pseudotyping retroviral vectors with VSV G. The same advantages of VSV G pseudotypes of HIV-1 apply to retroviral vectors; VSV G pseudotyped retroviral vectors may be used to introduce genes of interest into a wide variety of cell lines. (C) 1997 Academic Press.
引用
收藏
页码:337 / 342
页数:6
相关论文
共 9 条
[1]   Human immunodeficiency virus type 1 cell cycle control: Vpr is cytostatic and mediates G(2) accumulation by a mechanism which differs from DNA damage checkpoint control [J].
Bartz, SR ;
Rogel, ME ;
Emerman, M .
JOURNAL OF VIROLOGY, 1996, 70 (04) :2324-2331
[2]   VESICULAR STOMATITIS-VIRUS G GLYCOPROTEIN PSEUDOTYPED RETROVIRAL VECTORS - CONCENTRATION TO VERY HIGH-TITER AND EFFICIENT GENE-TRANSFER INTO MAMMALIAN AND NONMAMMALIAN CELLS [J].
BURNS, JC ;
FRIEDMANN, T ;
DRIEVER, W ;
BURRASCANO, M ;
YEE, JK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :8033-8037
[3]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[4]   DETECTION OF REPLICATION-COMPETENT AND PSEUDOTYPED HUMAN-IMMUNODEFICIENCY-VIRUS WITH A SENSITIVE CELL-LINE ON THE BASIS OF ACTIVATION OF AN INTEGRATED BETA-GALACTOSIDASE GENE [J].
KIMPTON, J ;
EMERMAN, M .
JOURNAL OF VIROLOGY, 1992, 66 (04) :2232-2239
[5]  
MILLER AD, 1989, BIOTECHNIQUES, V7, P980
[6]   ADVANCED MAMMALIAN GENE-TRANSFER - HIGH TITER RETROVIRAL VECTORS WITH MULTIPLE-DRUG SELECTION MARKERS AND A COMPLEMENTARY HELPER-FREE PACKAGING CELL-LINE [J].
MORGENSTERN, JP ;
LAND, H .
NUCLEIC ACIDS RESEARCH, 1990, 18 (12) :3587-3596
[7]   CHANGES IN GROWTH-PROPERTIES ON PASSAGE IN TISSUE-CULTURE OF VIRUSES DERIVED FROM INFECTIOUS MOLECULAR CLONES OF HIV-1LAI, HIV-1MAL, AND HIV-1ELI [J].
PEDEN, K ;
EMERMAN, M ;
MONTAGNIER, L .
VIROLOGY, 1991, 185 (02) :661-672
[8]   THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VPR GENE PREVENTS CELL-PROLIFERATION DURING CHRONIC INFECTION [J].
ROGEL, ME ;
WU, LI ;
EMERMAN, M .
JOURNAL OF VIROLOGY, 1995, 69 (02) :882-888
[9]  
YEE JK, 1994, METHOD CELL BIOL, V43, P99