• Je něco špatně v tomto záznamu ?

Biophysical properties of cationic lipophosphoramidates: Vesicle morphology, bilayer hydration and dynamics

D. Loizeau, P. Jurkiewicz, G. Aydogan, AA. Philimonenko, S. Mahfoudhi, P. Hozák, A. Maroto, H. Couthon-Gourvès, PA. Jaffrès, L. Deschamps, P. Giamarchi, M. Hof,

. 2015 ; 136 (-) : 192-200. [pub] 20150910

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc16028190

Cationic lipids are used to deliver genetic material to living cells. Their proper biophysical characterization is needed in order to design and control this process. In the present work we characterize some properties of recently synthetized cationic lipophosphoramidates. The studied compounds share the same structure of their hydrophobic backbone, but differ in their hydrophilic cationic headgroup, which is formed by a trimethylammonium, a trimethylarsonium or a dicationic moiety. Dynamic light scattering and cryo-transmission electron microscopy proves that the studied lipophosphoramidates create stable unilamellar vesicles. Fluorescence of polarity probe, Laurdan, analyzed using time-dependent fluorescence shift method (TDFS) and generalized polarization (GP) gives important information about the phase, hydration and dynamics of the lipophosphoramidate bilayers. While all of the compounds produced lipid bilayers that were sufficiently fluid for their potential application in gene therapy, their polarity/hydration and mobility was lower than for the standard cationic lipid - DOTAP. Mixing cationic lipophosphoramidates with DOPC helps to reduce this difference. The structure of the cationic headgroup has an important and complex influence on bilayer hydration and mobility. Both TDFS and GP methods are suitable for the characterization of cationic amphiphiles and can be used for screening of the newly synthesized compounds.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16028190
003      
CZ-PrNML
005      
20161021111133.0
007      
ta
008      
161005s2015 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.colsurfb.2015.09.012 $2 doi
024    7_
$a 10.1016/j.colsurfb.2015.09.012 $2 doi
035    __
$a (PubMed)26398144
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Loizeau, Damien $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
245    10
$a Biophysical properties of cationic lipophosphoramidates: Vesicle morphology, bilayer hydration and dynamics / $c D. Loizeau, P. Jurkiewicz, G. Aydogan, AA. Philimonenko, S. Mahfoudhi, P. Hozák, A. Maroto, H. Couthon-Gourvès, PA. Jaffrès, L. Deschamps, P. Giamarchi, M. Hof,
520    9_
$a Cationic lipids are used to deliver genetic material to living cells. Their proper biophysical characterization is needed in order to design and control this process. In the present work we characterize some properties of recently synthetized cationic lipophosphoramidates. The studied compounds share the same structure of their hydrophobic backbone, but differ in their hydrophilic cationic headgroup, which is formed by a trimethylammonium, a trimethylarsonium or a dicationic moiety. Dynamic light scattering and cryo-transmission electron microscopy proves that the studied lipophosphoramidates create stable unilamellar vesicles. Fluorescence of polarity probe, Laurdan, analyzed using time-dependent fluorescence shift method (TDFS) and generalized polarization (GP) gives important information about the phase, hydration and dynamics of the lipophosphoramidate bilayers. While all of the compounds produced lipid bilayers that were sufficiently fluid for their potential application in gene therapy, their polarity/hydration and mobility was lower than for the standard cationic lipid - DOTAP. Mixing cationic lipophosphoramidates with DOPC helps to reduce this difference. The structure of the cationic headgroup has an important and complex influence on bilayer hydration and mobility. Both TDFS and GP methods are suitable for the characterization of cationic amphiphiles and can be used for screening of the newly synthesized compounds.
650    _2
$a kationty $7 D002412
650    _2
$a fluorescenční polarizace $7 D005454
650    _2
$a lipidové dvojvrstvy $x chemie $7 D008051
650    _2
$a transmisní elektronová mikroskopie $x metody $7 D046529
650    _2
$a organofosforové sloučeniny $x chemie $7 D009943
650    _2
$a voda $x chemie $7 D014867
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Jurkiewicz, Piotr $u J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, v. v. i., Dolejškova 3, 18223 Prague 8, Czech Republic.
700    1_
$a Aydogan, Gokcan $u J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, v. v. i., Dolejškova 3, 18223 Prague 8, Czech Republic. $7 gn_A_00010568
700    1_
$a Philimonenko, Anatoly A $u Institute of Molecular Genetics of the ASCR, v.v.i., Laboratory of Biology of the Cell Nucleus, Vídeňská 1083, 142 20 Prague 4, Czech Republic.
700    1_
$a Mahfoudhi, Selim $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
700    1_
$a Hozák, Pavel $u Institute of Molecular Genetics of the ASCR, v.v.i., Laboratory of Biology of the Cell Nucleus, Vídeňská 1083, 142 20 Prague 4, Czech Republic.
700    1_
$a Maroto, Alicia $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
700    1_
$a Couthon-Gourvès, Hélène $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
700    1_
$a Jaffrès, Paul-Alain $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
700    1_
$a Deschamps, Laure $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
700    1_
$a Giamarchi, Philippe $u UMR CNRS 6521, SFR 148 ScInBIoS, Université de Brest, Université Européenne de Bretagne, 6 Avenue Le Gorgeu, 29238 Brest, France.
700    1_
$a Hof, Martin $u J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, v. v. i., Dolejškova 3, 18223 Prague 8, Czech Republic. Electronic address: martin.hof@jh-inst.cas.cz.
773    0_
$w MED00180202 $t Colloids and surfaces. B, Biointerfaces $x 1873-4367 $g Roč. 136, č. - (2015), s. 192-200
856    41
$u https://pubmed.ncbi.nlm.nih.gov/26398144 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20161005 $b ABA008
991    __
$a 20161021111541 $b ABA008
999    __
$a ok $b bmc $g 1166504 $s 952820
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 136 $c - $d 192-200 $e 20150910 $i 1873-4367 $m Colloids and surfaces. B, Biointerfaces $n Colloids surf., B Biointerfaces $x MED00180202
LZP    __
$a Pubmed-20161005

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...