Cell Engineering

1. Front Matter

   Pages i-vii

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2. Application of Recombinant Baculoviruses in Biopharmaceutical Research

   • T. A. Kost, J. L. Klein, J. P. Condreay

   Pages 1-28

3. Engineering Post-Translational Processing of Recombinant Proteins Produced in Insect Cell Culture

   • E. Ailor, M. J. Betenbaugh

   Pages 29-42

4. A Guide to Successful Scale-up of the Baculovirus Expression System

   • C. Mannix, R. F. Jarman

   Pages 43-55

5. Transient Gene Expression in Mammalian Cells Based on the Calcium Phosphate Transfection Method

   • M. Jordan

   Pages 56-79

6. Adenovirus Vectors in Functional Genomics

   • Wahiba Oualikene, Bernard Massie

   Pages 80-154

7. Adeno-Associated Virus: A Promising Tool for Gene Delivery

   • A. M. Douar

   Pages 155-181

8. Alphavirus Vectors: Highly Efficient Systems for Transient Gene Expression

   • C. Smerdou, P. Liljeström

   Pages 182-210

9. Transient Expression in Mammalian Cells : Applications and Perspectives

   • Alain R. Bernard

   Pages 211-218

10. Back Matter

    Pages 219-223

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The advantages of the baculovirus system are rooted in the properties of the virus and the host (insect, or cell lines derived from it). During the normal infection cycle, two forms of the virus are produced: an early budded virus (BY) form (Kost et al. , 2000), in which the viral DNA and structural proteins are surrounded by membrane derived from the infected cell; and a late occluded form (occlusion-derived virus, ODy), consisting of enveloped viral cores which are embedded in a crystal matrix of viral proteins. The principal component of the matrix is the abundantly expressed protein polyhedrin. The budded virus rapidly spreads the infection from cell to cell within the insect host, resulting ultimately in the complete liquefaction of the host, and release of occluded virus into the environment. The occluded form protects the released virus, allowing it to survive for long periods in the environment until ingested by another host. In the alkaline environment ofthe insect gut, the protective protein matrix is removed, and the life cycle is repeated. In insect cell cultures, only the BV form of baculovirus is required, and the polyhedrin gene may be replaced with the gene for the recombinant protein. An additional benefit of replacing or deleting polyhedrin is that it effectively makes the virus unable to survive outside the laboratory, an advantage in terms of environmental safety. The system is intrinsically safe to animals, being unable to replicate in species other than a limited range of insects.

• Calcium
• DNA
• Expression
• Mammalia
• Translation
• Viruses
• Vivo
• development
• gene expression
• gene therapy
• proteins
• biochemical engineering

• School of Chemical Engineering, The University of Birmingham, Edgbaston, Birmingham, UK

  Mohamed Al-Rubeai

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