Literature DB >> 14529353

Protein transduction domains and their utility in gene therapy.

A M J Beerens1, A F Y Al Hadithy, M G Rots, H J Haisma.   

Abstract

Protein transduction domains (PTDs, sometimes termed cell permeable proteins (CPP) or membrane translocating sequences (MTS)) are small peptides that are able to ferry much larger molecules into cells independent of classical endocytosis. This property makes PTDs ideal tools to transfer proteins and other molecules into living cells for research purposes. The mechanism by which this internalization takes place is poorly understood. It is evident, however, that many known PTDs bind to the same surface molecules (Heparan Sulphate Proteoglycans, HSPG) before internalization, and that internalization is dependent on these molecules. PTDs, although at this moment mainly used for the chemical or bacterial production of membrane permeable proteins can become powerful tools for gene therapy. By incorporating a PTD in the therapeutic gene product, the protein produced in the transfected cell might be enabled to spread to non-transfected cells, thereby creating an increased therapeutic effect. In this review, we give an overview of PTDs that may be useful for gene therapy applications, and discuss some of the problems that can be expected when incorporating PTDs in gene therapy approaches.

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Year:  2003        PMID: 14529353     DOI: 10.2174/1566523034578258

Source DB:  PubMed          Journal:  Curr Gene Ther        ISSN: 1566-5232            Impact factor:   4.391


  5 in total

1.  Generation of mouse induced pluripotent stem cells by protein transduction.

Authors:  Csilla Nemes; Eszter Varga; Zsuzsanna Polgar; Nuttha Klincumhom; Melinda K Pirity; Andras Dinnyes
Journal:  Tissue Eng Part C Methods       Date:  2013-10-12       Impact factor: 3.056

2.  Polyarginine as a multifunctional fusion tag.

Authors:  Stephen M Fuchs; Ronald T Raines
Journal:  Protein Sci       Date:  2005-06       Impact factor: 6.725

3.  Development of a cell permeable competitive antagonist of RhoA and CRMP4 binding, TAT-C4RIP, to promote neurite outgrowth.

Authors:  Mohammad R Khazaei; Samuel Montcalm; Adriana Di Polo; Alyson E Fournier; Yves Durocher; Stephan Ong Tone
Journal:  J Mol Neurosci       Date:  2015-02       Impact factor: 3.444

4.  Combination of therapeutic hypothermia and other neuroprotective strategies after an ischemic cerebral insult.

Authors:  Joline Goossens; Saïd Hachimi-Idrissi
Journal:  Curr Neuropharmacol       Date:  2014-09       Impact factor: 7.363

5.  Cell-Permeable Peptide Targeting the Nrf2-Keap1 Interaction: A Potential Novel Therapy for Global Cerebral Ischemia.

Authors:  Jingyi Tu; Xi Zhang; Ying Zhu; Yongxin Dai; Ning Li; Fang Yang; Quanguang Zhang; Darrell W Brann; Ruimin Wang
Journal:  J Neurosci       Date:  2015-11-04       Impact factor: 6.167

  5 in total

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