Adenovirus Dodecahedron, a VLP, Can be Purified by Size Exclusion Chromatography Instead of Time-Consuming Sucrose Density Gradient Centrifugation
Adenoviral dodecahedron (Dd) is a virus-like particle composed of twelve pentameric penton base (Pb) proteins, responsible for adenovirus cell penetration. It is generated spontaneously in the baculovirus system upon expression of the Pb gene of adenovirus serotype 3. This particle shows remarkable...
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description | Adenoviral dodecahedron (Dd) is a virus-like particle composed of twelve pentameric penton base (Pb) proteins, responsible for adenovirus cell penetration. It is generated spontaneously in the baculovirus system upon expression of the Pb gene of adenovirus serotype 3. This particle shows remarkable cell penetration ability with 2,00,000–3,00,000 Dd internalized into one cell in culture, conceivably delivering several millions of foreign cargo molecules to the target cell. We have used it in the past for delivery of small drugs as well as a vaccination platform, in which Dd serves as a particulate vaccine delivery system. Since development of new biomedicals depends strongly on the cost of their expression and purification, we attempted, albeit unsuccessfully, to obtain Dd expression in bacteria. We therefore retained its expression in the baculovirus/insect cells system but introduced significant improvements in the protocols for Dd expression and purification, leading to considerable savings in time and improved yield. |
doi_str_mv | 10.1007/s12033-015-9850-9 |
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It is generated spontaneously in the baculovirus system upon expression of the Pb gene of adenovirus serotype 3. This particle shows remarkable cell penetration ability with 2,00,000–3,00,000 Dd internalized into one cell in culture, conceivably delivering several millions of foreign cargo molecules to the target cell. We have used it in the past for delivery of small drugs as well as a vaccination platform, in which Dd serves as a particulate vaccine delivery system. Since development of new biomedicals depends strongly on the cost of their expression and purification, we attempted, albeit unsuccessfully, to obtain Dd expression in bacteria. 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It is generated spontaneously in the baculovirus system upon expression of the Pb gene of adenovirus serotype 3. This particle shows remarkable cell penetration ability with 2,00,000–3,00,000 Dd internalized into one cell in culture, conceivably delivering several millions of foreign cargo molecules to the target cell. We have used it in the past for delivery of small drugs as well as a vaccination platform, in which Dd serves as a particulate vaccine delivery system. Since development of new biomedicals depends strongly on the cost of their expression and purification, we attempted, albeit unsuccessfully, to obtain Dd expression in bacteria. We therefore retained its expression in the baculovirus/insect cells system but introduced significant improvements in the protocols for Dd expression and purification, leading to considerable savings in time and improved yield.</description><subject>Adenoviridae - genetics</subject><subject>Adenoviridae - metabolism</subject><subject>Adenoviruses</subject><subject>Biochemistry</subject><subject>Biological Techniques</subject><subject>Biotechnology</subject><subject>Cell Biology</subject><subject>Centrifugation</subject><subject>Centrifugation - methods</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatography</subject><subject>Chromatography, Gel - methods</subject><subject>Cloning, Molecular</subject><subject>E coli</subject><subject>Escherichia coli - genetics</subject><subject>Genes, Viral</subject><subject>Human Genetics</subject><subject>Immunization</subject><subject>Protein Science</subject><subject>Proteins</subject><subject>Sucrose</subject><subject>Vaccines</subject><subject>Viral Proteins - 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Academic</collection><jtitle>Molecular biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Szurgot, I.</au><au>Jedynak, M.</au><au>Podsiadla-Bialoskorska, M.</au><au>Piwowarski, Jan</au><au>Szolajska, E.</au><au>Chroboczek, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenovirus Dodecahedron, a VLP, Can be Purified by Size Exclusion Chromatography Instead of Time-Consuming Sucrose Density Gradient Centrifugation</atitle><jtitle>Molecular biotechnology</jtitle><stitle>Mol Biotechnol</stitle><addtitle>Mol Biotechnol</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>57</volume><issue>6</issue><spage>565</spage><epage>573</epage><pages>565-573</pages><issn>1073-6085</issn><eissn>1559-0305</eissn><abstract>Adenoviral dodecahedron (Dd) is a virus-like particle composed of twelve pentameric penton base (Pb) proteins, responsible for adenovirus cell penetration. It is generated spontaneously in the baculovirus system upon expression of the Pb gene of adenovirus serotype 3. This particle shows remarkable cell penetration ability with 2,00,000–3,00,000 Dd internalized into one cell in culture, conceivably delivering several millions of foreign cargo molecules to the target cell. We have used it in the past for delivery of small drugs as well as a vaccination platform, in which Dd serves as a particulate vaccine delivery system. Since development of new biomedicals depends strongly on the cost of their expression and purification, we attempted, albeit unsuccessfully, to obtain Dd expression in bacteria. We therefore retained its expression in the baculovirus/insect cells system but introduced significant improvements in the protocols for Dd expression and purification, leading to considerable savings in time and improved yield.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>25711740</pmid><doi>10.1007/s12033-015-9850-9</doi><tpages>9</tpages></addata></record> |
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subjects | Adenoviridae - genetics Adenoviridae - metabolism Adenoviruses Biochemistry Biological Techniques Biotechnology Cell Biology Centrifugation Centrifugation - methods Chemistry Chemistry and Materials Science Chromatography Chromatography, Gel - methods Cloning, Molecular E coli Escherichia coli - genetics Genes, Viral Human Genetics Immunization Protein Science Proteins Sucrose Vaccines Viral Proteins - genetics Viral Proteins - isolation & purification Viral Proteins - metabolism |
title | Adenovirus Dodecahedron, a VLP, Can be Purified by Size Exclusion Chromatography Instead of Time-Consuming Sucrose Density Gradient Centrifugation |
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