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        A Practical Guide for using the AdEasy System

        互联网

        1135

        Tong-Chuan He, Kenneth W. Kinzler, and Bert Vogelstein
        Howard Hughes Medical Institute
        and Molecular Genetics Laboratory
        Johns Hopkins Oncology Center
        424 North Bond Street
        Baltimore, MD 21231, USA
        Tel: (410)955-8886
        Fax: (410)955-0548

        vogelbe@welchlink.welch.jhu.edu
        kinzlke@welchlink.welch.jhu.edu
        t_c_he@yahoo.com

        I. Introduction

        Summary
        Recombinant adenoviruses provide a versatile system for gene expression studies and therapeutic applications. We here report a strategy which simplifies the generation and production of such viruses. A recombinant adenoviral plasmid is generated with a minimum of enzymatic manipulations, employing homologous recombination in bacteria rather than in eucaryotic cells. Following transfections of such plasmids into a mammalian packaging cell line, viral production is conveniently followed with the aid of green fluorescent protein, encoded by a gene incorporated into the viral backbone. Homogeneous viruses can be obtained from this procedure without plaque purification. This system should expedite the process of generating and testing recombinant adenoviruses for a variety of purposes.

        Outline of the AdEasy system

        A Practical Guide for using the AdEasy System

        Schematic Outline of the AdEasy System. The gene of interest is first cloned into a shuttle vector, e.g. pAdTrack-CMV. The resultant plasmid is linearized by digesting with restriction endonuclease Pme I, and subsequently cotransformed into E. coli. BJ5183 cells with an adenoviral backbone plasmid, e.g. pAdEasy-1,. Recombinants are selected for kanamycin resistance, and recombination confirmed by restriction endonuclease analyses. Finally, the linearized recombinant plasmid is transfected into adenovirus packaging cell lines, e.g. 293 cells. Recombinant adenoviruses are typically generated within 7 to 12 days. The "left arm" and "right arm" represent the regions mediating homologous recombination between the shuttle vector and the adenoviral backbone vector. An: polyadenylation site; Bm: BamHI, RI: EcoRI; LITR: left-hand ITR and packaging signal; RITR: right-hand ITR; Sp: SpeI.

         

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