Literature DB >> 12533777

Real-time observation of lipoplex formation and interaction with anionic bilayer vesicles.

S P Pantazatos1, R C MacDonald.   

Abstract

A novel development has allowed for the direct observation of single, pairwise interactions of linear DNA with cationic vesicles and of DNA-cationic lipid complexes with anionic vesicles. A new cationic phospholipid derivative, l,2-dioleoyl-sn-glycero-3-ethylphosphocholine, was used to prepare giant bilayer vesicles and to form DNA-cationic lipid complexes (lipoplexes). The cationic vesicles were electrophoretically maneuvered into contact with DNA, and similarly, complexes were brought into contact with anionic phospholipid vesicles composed of dioleoylphosphatidylglycerol (DOPG; 100%), DOPG/dioleoylphosphatidylethanolamine (DOPE; 1:1) or DOPG/dioleoylphosphatidylcholine (DOPC; 1:1). Video fluorescence microscopy revealed that upon contact with phospholipid anionic vesicles, lipoplexes exhibited four different types of behavior: adhesion, vesicle rupture, membrane perforation (manifested as vesicle shrinkage and/or content loss), and expansion of DNA (which was always concomitant with membrane perforation.) In one instance, the lipoplex was injected into the target vesicle just prior to DNA expansion. In all other instances, the DNA expanded over the outer surface of the vesicle, and expansion was faster, the larger the area of vesicle over which it expanded. Given the likelihood of incorporation of cellular anionic lipids into lipoplexes, the expansion of the DNA could be important in DNA release during cell transfection. Upon contact with naked DNA, giant cationic vesicles usually ruptured and condensed the DNA into a small particle. Contact of cationic vesicles that were partially coated with DNA usually caused the DNA to wrap around the vesicle, leading to vesicle rupture, vesicle fusion (with other attached vesicles or lipid aggregates), or simply cessation of movement. These behaviors clearly indicated that both DNA and vesicles could be partly or fully covered by the other, thus modifying surface charges, which, among others, allowed adhesion of DNA-coated vesicles with uncoated vesicles and of lipid-coated DNA with uncoated DNA.

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Year:  2003        PMID: 12533777     DOI: 10.1007/s00232-002-1050-4

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  6 in total

1.  Mechanisms of lipoplex formation: dependence of the biological properties of transfection complexes on formulation procedures.

Authors:  V A Rakhmanova; E V Pozharski; R C MacDonald
Journal:  J Membr Biol       Date:  2004-07-01       Impact factor: 1.843

2.  The effect of PS content on the ability of natural membranes to fuse with positively charged liposomes and lipoplexes.

Authors:  K Stebelska; P M Dubielecka; A F Sikorski
Journal:  J Membr Biol       Date:  2005-08       Impact factor: 1.843

3.  N4,N9-dioleoyl spermine is a novel nonviral lipopolyamine vector for plasmid DNA formulation.

Authors:  Osama A A Ahmed; Noppadon Adjimatera; Charareh Pourzand; Ian S Blagbrough
Journal:  Pharm Res       Date:  2005-06-08       Impact factor: 4.200

4.  Lipoplex formulation of superior efficacy exhibits high surface activity and fusogenicity, and readily releases DNA.

Authors:  Rumiana Koynova; Yury S Tarahovsky; Li Wang; Robert C MacDonald
Journal:  Biochim Biophys Acta       Date:  2006-11-01

5.  DNA release from lipoplexes by anionic lipids: correlation with lipid mesomorphism, interfacial curvature, and membrane fusion.

Authors:  Yury S Tarahovsky; Rumiana Koynova; Robert C MacDonald
Journal:  Biophys J       Date:  2004-08       Impact factor: 4.033

6.  Bilayer mixing, fusion, and lysis following the interaction of populations of cationic and anionic phospholipid bilayer vesicles.

Authors:  D P Pantazatos; S P Pantazatos; R C MacDonald
Journal:  J Membr Biol       Date:  2003-07-15       Impact factor: 1.843

  6 in total

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