Literature DB >> 10343913

Water-soluble, meso-substituted cationic porphyrins--a family of compounds for cellular delivery of oligonucleotides.

S M Flynn1, S T George, L White, W Devonish, G B Takle.   

Abstract

The delivery of oligonucleotides to appropriate intracellular compartments is crucial to their development as tools in gene function studies and as therapeutics. Here, we report the characterization of meso-substituted cationic porphyrins as a large class of water-soluble reagents for oligonucleotide delivery. These porphyrins form non-covalent complexes with single-stranded oligonucleotides and deliver these molecules into the nuclei of cell lines in culture. The porphyrins protect oligonucleotides from nuclease degradation, and delivery is unaffected by the presence of serum. Delivery capacity is dependent on the charge ratio and concentration of the oligonucleotide and porphyrin used to form the complex, on the chemical substituents of the oligonucleotide and on the identity of the cationic porphyrin. This class of molecules provides a versatile set of water-soluble delivery reagents that could contribute to the development of oligonucleotide drugs.

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Year:  1999        PMID: 10343913     DOI: 10.2144/99264rr03

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  3 in total

1.  Erratum to: Axial imidazole binding strengths in porphyrinoid cobalt(III) complexes as studied by tandem mass spectrometry.

Authors:  Ekta Mishra; Jill L Worlinsky; Thomas M Gilbert; Christian Brückner; Victor Ryzhov
Journal:  J Am Soc Mass Spectrom       Date:  2012-06-12       Impact factor: 3.109

2.  Axial imidazole binding strengths in porphyrinoid cobalt(III) complexes as studied by tandem mass spectrometry.

Authors:  Ekta Mishra; Jill L Worlinsky; Thomas M Gilbert; Christian Brückner; Victor Ryzhov
Journal:  J Am Soc Mass Spectrom       Date:  2012-04-12       Impact factor: 3.109

3.  The porphyrin TmPyP4 unfolds the extremely stable G-quadruplex in MT3-MMP mRNA and alleviates its repressive effect to enhance translation in eukaryotic cells.

Authors:  Mark J Morris; Katherine L Wingate; Jagannath Silwal; Thomas C Leeper; Soumitra Basu
Journal:  Nucleic Acids Res       Date:  2012-01-20       Impact factor: 16.971

  3 in total

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