Literature DB >> 11175311

Photoactivatable retroviral vectors: a strategy for targeted gene delivery.

M W Pandori1, T Sano.   

Abstract

We have explored a novel strategy for the targeting of retroviral vectors to particular sites or cell types. This strategy involves a method whereby the infectivity of a retroviral vector is neutralized by treatment of viral particles with a photocleavable, biotinylation reagent. These modified viral vectors possess little to no infectivity for target cells. Exposure of these modified viral vectors to long-wavelength UV light induces a reversal of the neutralizing, chemical modification resulting in restoration of infectivity to the viral vector. This infectivity 'trigger' possesses great potential, both as a research tool and as a novel tactic for the targeting of gene-transfer agents, since it would become possible to direct both the time and location of a viral infection in a versatile manner.

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Year:  2000        PMID: 11175311     DOI: 10.1038/sj.gt.3301338

Source DB:  PubMed          Journal:  Gene Ther        ISSN: 0969-7128            Impact factor:   5.250


  3 in total

Review 1.  Gene therapy for glioblastoma: future perspective for delivery systems and molecular targets.

Authors:  A Shir; A Levitzki
Journal:  Cell Mol Neurobiol       Date:  2001-12       Impact factor: 5.046

Review 2.  Stimulus-responsive viral vectors for controlled delivery of therapeutics.

Authors:  Mitchell J Brun; Eric J Gomez; Junghae Suh
Journal:  J Control Release       Date:  2017-08-24       Impact factor: 9.776

3.  Spatiotemporally confined red light-controlled gene delivery at single-cell resolution using adeno-associated viral vectors.

Authors:  Maximilian Hörner; Carolina Jerez-Longres; Anna Hudek; Sebastian Hook; O Sascha Yousefi; Wolfgang W A Schamel; Cindy Hörner; Matias D Zurbriggen; Haifeng Ye; Hanna J Wagner; Wilfried Weber
Journal:  Sci Adv       Date:  2021-06-16       Impact factor: 14.136

  3 in total

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