Protein transduction into human cells by adenovirus dodecahedron using WW domains as universal adaptors
- 3 January 2006
- journal article
- research article
- Published by Wiley in The Journal of Gene Medicine
- Vol. 8 (4) , 524-531
- https://doi.org/10.1002/jgm.862
Abstract
Background Direct protein transduction is a recent technique that involves use of peptide vectors. In this study, we demonstrate that adenovirus dodecahedron (Dd), a virus‐like particle devoid of DNA and able to penetrate cells with high efficiency, can be used as a vector for protein delivery. Methods Taking advantage of Dd interaction with structural domains called WW, we have elaborated a universal adaptor to attach a protein of interest to this vector. Results A tandem of three WW structural domains derived from the Nedd4 protein enables the formation of stable complexes with Dd, without impairing its endocytosis efficiency. Our protein of interest fused to the triple WW linker is delivered by the dodecahedron in 100% of cells in culture with on average more than ten million molecules per cell. Conclusion These data demonstrate the great potential of adenovirus dodecahedron in combination with WW domains as a protein transduction vector. Copyright © 2006 John Wiley & Sons, Ltd.Keywords
This publication has 33 references indexed in Scilit:
- Adenovirus Dodecahedron Allows Large Multimeric Protein Transduction in Human CellsJournal of Virology, 2003
- There Are Two Different Species B Adenovirus Receptors: sBAR, Common to Species B1 and B2 Adenoviruses, and sB2AR, Exclusively Used by Species B2 AdenovirusesJournal of Virology, 2003
- Adenovirus Protein Involved in Virus Internalization Recruits Ubiquitin−Protein LigasesBiochemistry, 2002
- 3PO, a novel nonviral gene delivery system using engineered Ad5 penton proteinsGene Therapy, 2001
- Protein transduction: an alternative to genetic intervention?Gene Therapy, 2001
- Adenovirus dodecahedron, a new vector for human gene transferNature Biotechnology, 1997
- Structure of the WW domain of a kinase-associated protein complexed with a proline-rich peptideNature, 1996
- Integrins αvβ3 and αvβ5 promote adenovirus internalization but not virus attachmentCell, 1993
- Cellular uptake of the tat protein from human immunodeficiency virusCell, 1988
- Autonomous functional domains of chemically synthesized human immunodeficiency virus tat trans-activator proteinCell, 1988