2012
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Photofoams: Remote Control of Foam Destabilization by Exposure to Light Using an Azobenzene Surfactant Article de journal E Chevallier; C Monteux; F Lequewx; C Tribet Langmuir, 28 , p. 2308-2312, 2012, ISSN: 0743-7463. @article{RN12b,
title = {Photofoams: Remote Control of Foam Destabilization by Exposure to Light Using an Azobenzene Surfactant},
author = {E Chevallier and C Monteux and F Lequewx and C Tribet},
doi = {10.1021/la204200z},
issn = {0743-7463},
year = {2012},
date = {2012-01-01},
journal = {Langmuir},
volume = {28},
pages = {2308-2312},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
Reactive Protein-Repellent Surfaces for the Straightforward Attachment of Small Molecules up to Whole Cells Article de journal S F M van Dongen; J Janvore; S S van Berkel; E Marie; M Piel; C Tribet Chemical Science, 3 (10), p. 3000-3006, 2012, ISSN: 2041-6520. @article{vanDongen:2012,
title = {Reactive Protein-Repellent Surfaces for the Straightforward Attachment of Small Molecules up to Whole Cells},
author = {S F M {van Dongen} and J Janvore and S S {van Berkel} and E Marie and M Piel and C Tribet},
doi = {10.1039/c2sc20652h},
issn = {2041-6520},
year = {2012},
date = {2012-01-01},
journal = {Chemical Science},
volume = {3},
number = {10},
pages = {3000-3006},
abstract = {Here we present a readily accessible strategy for creating protein-resistant surfaces that contain azides, based on the spontaneous adsorption of a comb-like copolymer. Using a strain-promoted azide alkyne cycloaddition, we illustrate the single-step conjugation of various representatives of important applications, being the labelling with small organic molecules, capture of nanoparticles, attachment of native enzymes at a controlled density, and finally control of cell adhesion. We thus demonstrate that advanced biomaterials can be created in two straightforward steps without requiring additional reagents, which should make this strategy a valuable tool for researchers in diverse fields.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Here we present a readily accessible strategy for creating protein-resistant surfaces that contain azides, based on the spontaneous adsorption of a comb-like copolymer. Using a strain-promoted azide alkyne cycloaddition, we illustrate the single-step conjugation of various representatives of important applications, being the labelling with small organic molecules, capture of nanoparticles, attachment of native enzymes at a controlled density, and finally control of cell adhesion. We thus demonstrate that advanced biomaterials can be created in two straightforward steps without requiring additional reagents, which should make this strategy a valuable tool for researchers in diverse fields. |
Reverse Variation of Cloud Points of Light-Responsive Assemblies of Azobenzene-Modified Amphiphilic Polymers Article de journal E Marie; C Tribet Chemistry Letters, 41 , p. 1093-1095, 2012, ISSN: 0366-7022. @article{RN8g,
title = {Reverse Variation of Cloud Points of Light-Responsive Assemblies of Azobenzene-Modified Amphiphilic Polymers},
author = {E Marie and C Tribet},
doi = {10.1246/cl.2012.1093},
issn = {0366-7022},
year = {2012},
date = {2012-01-01},
journal = {Chemistry Letters},
volume = {41},
pages = {1093-1095},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
The Thermally Induced Aggregation of Immunoglobulin G in Solution Is Prevented by Amphipols Article de journal D W Ma; N Martin; A Herbet; D Boquet; C Tribet; F M Winnik Chemistry Letters, 41 , p. 1380-1382, 2012, ISSN: 0366-7022. @article{RN9l,
title = {The Thermally Induced Aggregation of Immunoglobulin G in Solution Is Prevented by Amphipols},
author = {D W Ma and N Martin and A Herbet and D Boquet and C Tribet and F M Winnik},
doi = {10.1246/cl.2012.1380},
issn = {0366-7022},
year = {2012},
date = {2012-01-01},
journal = {Chemistry Letters},
volume = {41},
pages = {1380-1382},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
Unfolding of cytochrome c upon interaction with azobenzene-modified copolymers Article de journal J Sun; J Ruchmann; A Pallier; L Jullien; M Desmadril; C Tribet Biomacromolecules, 13 (11), p. 3736–3746, 2012. @article{Sun:2012,
title = {Unfolding of cytochrome c upon interaction with azobenzene-modified copolymers},
author = {J Sun and J Ruchmann and A Pallier and L Jullien and M Desmadril and C Tribet},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84869024546&doi=10.1021%2fbm301200p&partnerID=40&md5=6a3192fce387a1fce6cb3df6a36f2c5d},
doi = {10.1021/bm301200p},
year = {2012},
date = {2012-01-01},
journal = {Biomacromolecules},
volume = {13},
number = {11},
pages = {3736--3746},
abstract = {Hydrophilic or amphiphilic macromolecules are common organic matrices used to encapsulate and protect fragile drugs such as proteins. Polymer cargoes are in addition designed for remote control of protein delivery, upon imparting the macromolecules with stimuli-responsive properties, such as light-triggered polarity switches. The effect of interaction between polymers and proteins on the stability of the proteins is, however, rarely investigated. Here we studied the unfolding/folding equilibrium of cytochrome c (cyt c) under its oxidized or reduced forms, in the presence of various amphiphilic copolymers (by circular dichroism and intrinsic fluorescence measurements). As models of stimuli-responsive amphiphilic chains, we considered poly(acrylic acid) derivatives, modified to contain hydrophobic, light-responsive azobenzene moieties. These copolymers are, thus, capable to develop both ionic (under their sodium forms at pH > 8) and hydrophobic associations with the basic protein cyt c (isoelectric point of 10.0). In aqueous buffer upon increasing urea concentrations, cyt c underwent unfolding, at [urea] of 9-10 M, which was analyzed under the framework of the equilibrium between two states (native-unfolded). In the presence of polymers, the native folding of cyt c was preserved at low concentrations of urea (typically <4M). However, the presence of polymers facilitated unfolding, which occurred at urea concentrations lowered by 2-4 M as compared to unfolding in the absence of polymers (polymer/cyt c ratio of 1:1 g/g). The predominant contribution of coulombic interactions was shown by both the lack of significant impact of the amount of (neutral) azobenzene moieties in the copolymers and the disappearance of destabilization at ionic strength higher than 150 mM. In addition, stability was similar to that of an isolated cyt c, in the presence of a neutral chain bearing acryloyl(oligoethyleneoxide) units instead of the ionized sodium acrylate moieties. DSC measurements showed that in the presence of polymers, cyt c is thermally unfolded in aqueous buffer at temperatures lowered by >20 °C as compared to thermal unfolding in the absence of polymers. Upon exposure to UV light, properties of the polymers chains were perturbed in situ, upon cis/trans isomerization of the azobenzene groups. In polymers displaying a photoresponsive polarity and hydrophobicity switch (conventional azobenzene), the stability of cyt c was not affected by the exposure to light. In contrast, when photoionization occurred (using an hydroxyl-azobenzene whose pKa can be photoshifted), unfolding was initiated upon exposure to light. Altogether, these results show that coulombic binding is a predominant driving force that facilitates unfolding in water/urea solutions. In regard to the design of light-responsive systems for protein handling and control of folding, we conclude that remote control of the coulombic interaction upon photoionization of chromophores can be more efficient than the more conventional photomodulation of polarity. © 2012 American Chemical Society.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Hydrophilic or amphiphilic macromolecules are common organic matrices used to encapsulate and protect fragile drugs such as proteins. Polymer cargoes are in addition designed for remote control of protein delivery, upon imparting the macromolecules with stimuli-responsive properties, such as light-triggered polarity switches. The effect of interaction between polymers and proteins on the stability of the proteins is, however, rarely investigated. Here we studied the unfolding/folding equilibrium of cytochrome c (cyt c) under its oxidized or reduced forms, in the presence of various amphiphilic copolymers (by circular dichroism and intrinsic fluorescence measurements). As models of stimuli-responsive amphiphilic chains, we considered poly(acrylic acid) derivatives, modified to contain hydrophobic, light-responsive azobenzene moieties. These copolymers are, thus, capable to develop both ionic (under their sodium forms at pH > 8) and hydrophobic associations with the basic protein cyt c (isoelectric point of 10.0). In aqueous buffer upon increasing urea concentrations, cyt c underwent unfolding, at [urea] of 9-10 M, which was analyzed under the framework of the equilibrium between two states (native-unfolded). In the presence of polymers, the native folding of cyt c was preserved at low concentrations of urea (typically <4M). However, the presence of polymers facilitated unfolding, which occurred at urea concentrations lowered by 2-4 M as compared to unfolding in the absence of polymers (polymer/cyt c ratio of 1:1 g/g). The predominant contribution of coulombic interactions was shown by both the lack of significant impact of the amount of (neutral) azobenzene moieties in the copolymers and the disappearance of destabilization at ionic strength higher than 150 mM. In addition, stability was similar to that of an isolated cyt c, in the presence of a neutral chain bearing acryloyl(oligoethyleneoxide) units instead of the ionized sodium acrylate moieties. DSC measurements showed that in the presence of polymers, cyt c is thermally unfolded in aqueous buffer at temperatures lowered by >20 °C as compared to thermal unfolding in the absence of polymers. Upon exposure to UV light, properties of the polymers chains were perturbed in situ, upon cis/trans isomerization of the azobenzene groups. In polymers displaying a photoresponsive polarity and hydrophobicity switch (conventional azobenzene), the stability of cyt c was not affected by the exposure to light. In contrast, when photoionization occurred (using an hydroxyl-azobenzene whose pKa can be photoshifted), unfolding was initiated upon exposure to light. Altogether, these results show that coulombic binding is a predominant driving force that facilitates unfolding in water/urea solutions. In regard to the design of light-responsive systems for protein handling and control of folding, we conclude that remote control of the coulombic interaction upon photoionization of chromophores can be more efficient than the more conventional photomodulation of polarity. © 2012 American Chemical Society. |
Well-defined critical association concentration and rapid adsorption at the air/water interface of a short amphiphilic polymer, amphipol A8-35: A study by förster resonance energy transfer and dynamic surface tension measurements Article de journal F Giusti; J -L Popot; C Tribet Langmuir, 28 (28), p. 10372–10380, 2012. @article{Giusti:2012,
title = {Well-defined critical association concentration and rapid adsorption at the air/water interface of a short amphiphilic polymer, amphipol A8-35: A study by f\"{o}rster resonance energy transfer and dynamic surface tension measurements},
author = {F Giusti and J -L Popot and C Tribet},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863935182&doi=10.1021%2fla300774d&partnerID=40&md5=92c696ed97d5b47ba8c5d09bf1ea160c},
doi = {10.1021/la300774d},
year = {2012},
date = {2012-01-01},
journal = {Langmuir},
volume = {28},
number = {28},
pages = {10372--10380},
abstract = {Amphipols (APols) are short amphiphilic polymers designed to handle membrane proteins (MPs) in aqueous solutions as an alternative to small surfactants (detergents). APols adsorb onto the transmembrane, hydrophobic surface of MPs, forming small, water-soluble complexes, in which the protein is biochemically stabilized. At variance with MP/detergent complexes, MP/APol ones remain stable even at extreme dilutions. Pure APol solutions self-associate into well-defined micelle-like globules comprising a few APol molecules, a rather unusual behavior for amphiphilic polymers, which typically form ill-defined assemblies. The best characterized APol to date, A8-35, is a random copolymer of acrylic acid, isopropylacrylamide, and octylacrylamide. In the present work, the concentration threshold for self-association of A8-35 in salty buffer (NaCl 100 mM, Tris/HCl 20 mM, pH 8.0) has been studied by F\"{o}rster resonance energy transfer (FRET) measurements and tensiometry. In a 1:1 mol/mol mixture of APols grafted with either rhodamine or 7-nitro-1,2,3-benzoxadiazole, the FRET signal as a function of A8-35 concentration is essentially zero below a threshold concentration of 0.002 g ·L-1 and increases linearly with concentration above this threshold. This indicates that assembly takes place in a narrow concentration interval around 0.002 g ·L-1. Surface tension measurements decreases regularly with concentration until a threshold of ca. 0.004 g ·L-1, beyond which it reaches a plateau at ca. 30 mN ·m-1. Within experimental uncertainties, the two techniques thus yield a comparable estimate of the critical self-assembly concentration. The kinetics of variation of the surface tension was analyzed by dynamic surface tension measurements in the time window 10 ms-100 s. The rate of surface tension decrease was similar in solutions of A8-35 and of the anionic surfactant sodium dodecylsulfate when both compounds were at a similar molar concentration of n-alkyl moieties. Overall, the solution properties of APol "micelles" (in salty buffer) appear surprisingly similar to those of the micelles formed by small, nonpolymeric surfactants, a feature that was not anticipated owing to the polymeric and polydisperse nature of A8-35. The key to the remarkable stability to dilution of A8-35 globules, likely to include also that of MP/APol complexes, lies accordingly in the low value of the critical self-association concentration as compared to that of small amphiphilic analogues. © 2012 American Chemical Society.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Amphipols (APols) are short amphiphilic polymers designed to handle membrane proteins (MPs) in aqueous solutions as an alternative to small surfactants (detergents). APols adsorb onto the transmembrane, hydrophobic surface of MPs, forming small, water-soluble complexes, in which the protein is biochemically stabilized. At variance with MP/detergent complexes, MP/APol ones remain stable even at extreme dilutions. Pure APol solutions self-associate into well-defined micelle-like globules comprising a few APol molecules, a rather unusual behavior for amphiphilic polymers, which typically form ill-defined assemblies. The best characterized APol to date, A8-35, is a random copolymer of acrylic acid, isopropylacrylamide, and octylacrylamide. In the present work, the concentration threshold for self-association of A8-35 in salty buffer (NaCl 100 mM, Tris/HCl 20 mM, pH 8.0) has been studied by Förster resonance energy transfer (FRET) measurements and tensiometry. In a 1:1 mol/mol mixture of APols grafted with either rhodamine or 7-nitro-1,2,3-benzoxadiazole, the FRET signal as a function of A8-35 concentration is essentially zero below a threshold concentration of 0.002 g ·L-1 and increases linearly with concentration above this threshold. This indicates that assembly takes place in a narrow concentration interval around 0.002 g ·L-1. Surface tension measurements decreases regularly with concentration until a threshold of ca. 0.004 g ·L-1, beyond which it reaches a plateau at ca. 30 mN ·m-1. Within experimental uncertainties, the two techniques thus yield a comparable estimate of the critical self-assembly concentration. The kinetics of variation of the surface tension was analyzed by dynamic surface tension measurements in the time window 10 ms-100 s. The rate of surface tension decrease was similar in solutions of A8-35 and of the anionic surfactant sodium dodecylsulfate when both compounds were at a similar molar concentration of n-alkyl moieties. Overall, the solution properties of APol "micelles" (in salty buffer) appear surprisingly similar to those of the micelles formed by small, nonpolymeric surfactants, a feature that was not anticipated owing to the polymeric and polydisperse nature of A8-35. The key to the remarkable stability to dilution of A8-35 globules, likely to include also that of MP/APol complexes, lies accordingly in the low value of the critical self-association concentration as compared to that of small amphiphilic analogues. © 2012 American Chemical Society. |
2011
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Amphipols From A to Z Article de journal J L Popot; T Althoff; D Bagnard; J L Baneres; P Bazzacco; E Billon-Denis; L J Catoire; P Champeil; D Charvolin; M J Cocco; G Cremel; T Dahmane; L M de la Maza; C Ebel; F Gabel; F Giusti; Y Gohon; E Goormaghtigh; E Guittet; J H Kleinschmidt; W Kuhlbrandt; C Le Bon; K L Martinez; M Picard; B Pucci; J N Sachs; C Tribet; C van Heijenoort; F Wien; F Zito; M Zoonens Annual Review of Biophysics, Vol 40, 40 , p. 379-408, 2011, ISSN: 1936-122X. @article{RN14b,
title = {Amphipols From A to Z},
author = {J L Popot and T Althoff and D Bagnard and J L Baneres and P Bazzacco and E {Billon-Denis} and L J Catoire and P Champeil and D Charvolin and M J Cocco and G Cremel and T Dahmane and L M {de la Maza} and C Ebel and F Gabel and F Giusti and Y Gohon and E Goormaghtigh and E Guittet and J H Kleinschmidt and W Kuhlbrandt and C Le Bon and K L Martinez and M Picard and B Pucci and J N Sachs and C Tribet and C {van Heijenoort} and F Wien and F Zito and M Zoonens},
issn = {1936-122X},
year = {2011},
date = {2011-01-01},
journal = {Annual Review of Biophysics, Vol 40},
volume = {40},
pages = {379-408},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
Enhanced Stability of Nanoemulsions Using Mixtures of Non-Ionic Surfactant and Amphiphilic Polyelectrolyte Article de journal J Galindo-Alvarez; K A Le; V Sadtler; P Marchal; P Perrin; C Tribet; E Marie; A Durand Colloids and Surfaces a-Physicochemical and Engineering Aspects, 389 , p. 237-245, 2011, ISSN: 0927-7757. @article{RN16b,
title = {Enhanced Stability of Nanoemulsions Using Mixtures of Non-Ionic Surfactant and Amphiphilic Polyelectrolyte},
author = {J {Galindo-Alvarez} and K A Le and V Sadtler and P Marchal and P Perrin and C Tribet and E Marie and A Durand},
doi = {10.1016/j.colsurfa.2011.08.021},
issn = {0927-7757},
year = {2011},
date = {2011-01-01},
journal = {Colloids and Surfaces a-Physicochemical and Engineering Aspects},
volume = {389},
pages = {237-245},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
High Water Solubility and Fold in Amphipols of Proteins with Large Hydrophobic Regions: Oleosins and Caleosin from Seed Lipid Bodies Article de journal Y Gohon; J D Vindigni; A Pallier; F Wien; H Celia; A Giuliani; C Tribet; T Chardot; P Briozzo Biochimica Et Biophysica Acta-Biomembranes, 1808 , p. 706-716, 2011. @article{RN15b,
title = {High Water Solubility and Fold in Amphipols of Proteins with Large Hydrophobic Regions: Oleosins and Caleosin from Seed Lipid Bodies},
author = {Y Gohon and J D Vindigni and A Pallier and F Wien and H Celia and A Giuliani and C Tribet and T Chardot and P Briozzo},
doi = {10.1016/j.bbamem.2010.12.002},
year = {2011},
date = {2011-01-01},
journal = {Biochimica Et Biophysica Acta-Biomembranes},
volume = {1808},
pages = {706-716},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
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Miniemulsion Polymerization Templates: A Systematic Comparison between Low Energy Emulsification (Near-PIT) and Ultrasound Emulsification Methods Article de journal J Galindo-Alvarez; D Boyd; P Marchal; C Tribet; P Perrin; E Marie-Begue; A Durand; V Sadtler Colloids and Surfaces a-Physicochemical and Engineering Aspects, 374 , p. 134-141, 2011, ISSN: 0927-7757. @article{RN17b,
title = {Miniemulsion Polymerization Templates: A Systematic Comparison between Low Energy Emulsification (Near-PIT) and Ultrasound Emulsification Methods},
author = {J {Galindo-Alvarez} and D Boyd and P Marchal and C Tribet and P Perrin and E {Marie-Begue} and A Durand and V Sadtler},
doi = {10.1016/j.colsurfa.2010.11.019},
issn = {0927-7757},
year = {2011},
date = {2011-01-01},
journal = {Colloids and Surfaces a-Physicochemical and Engineering Aspects},
volume = {374},
pages = {134-141},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
Photoinduced pH drops in water Article de journal M Emond; J Sun; J Grégoire; S Maurin; C Tribet; L Jullien Physical Chemistry Chemical Physics, 13 (14), p. 6493–6499, 2011. @article{Emond:2011,
title = {Photoinduced pH drops in water},
author = {M Emond and J Sun and J Gr\'{e}goire and S Maurin and C Tribet and L Jullien},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952973660&doi=10.1039%2fc0cp02464c&partnerID=40&md5=34514ef4944c4bfa7ef5ebac9963af48},
doi = {10.1039/c0cp02464c},
year = {2011},
date = {2011-01-01},
journal = {Physical Chemistry Chemical Physics},
volume = {13},
number = {14},
pages = {6493--6499},
abstract = {A 2-hydroxyazobenzene platform has been evaluated to photorelease protons in aqueous solutions. Three different systems relying on molecular, supramolecular and polymeric strategies have been investigated in order to tune the water solubility and the thermodynamic and kinetic properties. This paper first reports on the syntheses and the physico chemical analyses for each system. Subsequently, we show that the three strategies are appropriate to reversibly photo-generate tunable pH drops in water up to one pH unit amplitude and at the 10-100 s timescale, upon transient illumination at 365 nm. © 2011 the Owner Societies.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
A 2-hydroxyazobenzene platform has been evaluated to photorelease protons in aqueous solutions. Three different systems relying on molecular, supramolecular and polymeric strategies have been investigated in order to tune the water solubility and the thermodynamic and kinetic properties. This paper first reports on the syntheses and the physico chemical analyses for each system. Subsequently, we show that the three strategies are appropriate to reversibly photo-generate tunable pH drops in water up to one pH unit amplitude and at the 10-100 s timescale, upon transient illumination at 365 nm. © 2011 the Owner Societies. |
Photoresponse of Complexes between Surfactants and Azobenzene-Modified Polymers Accounting for the Random Distribution of Hydrophobic Side Groups Article de journal J Ruchmann; S C Sebai; C Tribet Macromolecules, 44 , p. 604-611, 2011, ISSN: 0024-9297. @article{RN13b,
title = {Photoresponse of Complexes between Surfactants and Azobenzene-Modified Polymers Accounting for the Random Distribution of Hydrophobic Side Groups},
author = {J Ruchmann and S C Sebai and C Tribet},
doi = {10.1021/ma1024544},
issn = {0024-9297},
year = {2011},
date = {2011-01-01},
journal = {Macromolecules},
volume = {44},
pages = {604-611},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
Pumping-out Photo-Surfactants from an Air-Water Interface Using Light Article de journal E Chevallier; A Mamane; H A Stone; C Tribet; F Lequeux; C Monteux Soft Matter, 7 , p. 7866-7874, 2011, ISSN: 1744-683X. @article{RN18b,
title = {Pumping-out Photo-Surfactants from an Air-Water Interface Using Light},
author = {E Chevallier and A Mamane and H A Stone and C Tribet and F Lequeux and C Monteux},
doi = {10.1039/c1sm05378g},
issn = {1744-683X},
year = {2011},
date = {2011-01-01},
journal = {Soft Matter},
volume = {7},
pages = {7866-7874},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
2010
|
Light-Responsiveness of C12E6/Polymer Complexes Swollen with Dodecane Article de journal E Rotureau; C Tribet; S Fouilloux; P Marchal; V Sadtler; E Marie-Begue; A Durand; P Perrin Journal of Physical Chemistry B, 114 , p. 13294-13303, 2010, ISSN: 1520-6106. @article{RN20b,
title = {Light-Responsiveness of C_{12}E_{6}/Polymer Complexes Swollen with Dodecane},
author = {E Rotureau and C Tribet and S Fouilloux and P Marchal and V Sadtler and E {Marie-Begue} and A Durand and P Perrin},
doi = {10.1021/jp106127w},
issn = {1520-6106},
year = {2010},
date = {2010-01-01},
journal = {Journal of Physical Chemistry B},
volume = {114},
pages = {13294-13303},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
Permeabilization of Lipid Membranes and Cells by a Light-Responsive Copolymer Article de journal Sarra Sebai; Sophie Cribier; Ali Karimi; Dominique Massotte; Christophe Tribet Langmuir, 26 , p. 14135-14141, 2010. @article{RN19b,
title = {Permeabilization of Lipid Membranes and Cells by a Light-Responsive Copolymer},
author = {Sarra Sebai and Sophie Cribier and Ali Karimi and Dominique Massotte and Christophe Tribet},
doi = {10.1021/la102456z},
year = {2010},
date = {2010-01-01},
journal = {Langmuir},
volume = {26},
pages = {14135-14141},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|