Literature DB >> 16525863

The nuclear pore complex: the gateway to successful nonviral gene delivery.

Marieke A E M van der Aa1, Enrico Mastrobattista, Ronald S Oosting, Wim E Hennink, Gerben A Koning, Daan J A Crommelin.   

Abstract

One of the limiting steps in the efficiency of nonviral gene delivery is transport of genetic material across the nuclear membrane. Trafficking of nuclear proteins from the cytoplasm into the nucleus occurs via the nuclear pore complex and is mediated by nuclear localization signals and their nuclear receptors. Several strategies employing this transport mechanism have been designed and explored to improve nonviral gene delivery. In this article, we review the mechanism of nuclear import through the nuclear pore complex and the strategies used to facilitate nuclear import of exogenous DNA and improve gene expression.

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Year:  2006        PMID: 16525863     DOI: 10.1007/s11095-005-9445-4

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  139 in total

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Journal:  Mol Cell Biol       Date:  1999-11       Impact factor: 4.272

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Journal:  Mol Biol Cell       Date:  1997-11       Impact factor: 4.138

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Journal:  J Cell Sci       Date:  1997-09       Impact factor: 5.285

9.  A nuclear localization domain in the hnRNP A1 protein.

Authors:  H Siomi; G Dreyfuss
Journal:  J Cell Biol       Date:  1995-05       Impact factor: 10.539

10.  The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import.

Authors:  Tobias C Walther; Helen S Pickersgill; Volker C Cordes; Martin W Goldberg; Terry D Allen; Iain W Mattaj; Maarten Fornerod
Journal:  J Cell Biol       Date:  2002-07-08       Impact factor: 10.539

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  29 in total

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7.  Overcoming nonviral gene delivery barriers: perspective and future.

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8.  Quantification of plasmid DNA copies in the nucleus after lipoplex and polyplex transfection.

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9.  Transportin mediates nuclear entry of DNA in vertebrate systems.

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Review 10.  Layered double hydroxide nanoparticles as cellular delivery vectors of supercoiled plasmid DNA.

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