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- Team D. Lévy. Functional and structural analysis of membrane proteins
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- concentration wave of E. coli bacteria in a microchannel
- Amphiphilic Poly(ethylene oxide)-block-poly(butadiene-graft-liquid crystal) Copolymers: Synthesis and Self-Assembly in Water
- Binding, reconstitution and 2D crystallization of membrane or soluble proteins onto functionalised lipid layer observed in situ
- collectively migrating epithelium biophys cover
- Fig 5. Non-conservation of network motifs
- Fig 4. Model of biomolecular networks under duplication-divergence evolution
- Fig 3. Whole genome duplications in evolution
- Fig 2. Novel nanostructures made of DsrA ncRNA of E.coli
- Fig 1. RNA synthetic biology
- Fig 1. RNA synthetic biology
- Fig 1. RNA synthetic biology
- Fig 4. Model of biomolecular networks under duplication-divergence evolution
- Fig 4. Model of biomolecular networks under duplication-divergence evolution
- Fig 5. Expansion of signaling networks by whole genome duplication
- Fig. 1 Motor oscillations
- Fig. 2 Tissue competition
- Fig. 2 Compétition entre tissus
- Fig. 1 Oscillations de moteurs moléculaires
- Expansion of signaling networks by whole genome duplication
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- Brigitte da Silva
- Giulia carzedda
- laurence turpin
- Agnes verin
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- Brigitte Da Silva
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- Fahima Faqir
- Jean-Hugues Codarbox
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- Functional and structural analysis of BmrC/BmrD abacterial heterodimeric MDR transporter
- Functional and structural analysis of BmrC/BmrD bacterial heterodimeric MDR transporter
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- Structural changes in liquid crystal polymer vesicles induced by temperature variation and magnetic fields
- Biocompatible gold nanorods for cancer research
- Self-assembly of amphiphilic liquid crystal block copolymers containing a cholesteryl mesogen: Effects of block ratio and solven
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- Smectic polymer micellar aggregates with temperature-controlled morphologies
- Smectic polymer micellar aggregates with temperature-controlled morphologies
- Smectic polymer micellar aggregates with temperature-controlled morphologies
- Smectic polymer micellar aggregates with temperature-controlled morphologies
- C. elegans sperm cell crawling on a substrate.
- Actin filled liposome
- Actin Beads and VASP
- C. elegans sperm cells transfected with fluorescent MSP
- Multilayered liposome observed by cryoEM
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- 2D crystals of BmrC/BmrD
- 2D crystals of BmrC/BmrD, a bacterial heterodimeric ABC transporter
- Multilayered liposome obserbed by cryoEM
- 2D crystals of Light Harversting Complex, LH2, from Rba. sphaeroides
- Single particle analysis of 300kDa LH1-RC-PufX core complex of Rbs. veldkampii
- Atomic model of LH1-RC-PuhX from Rba. sphaeroides
- Atomic Model of LH1-RC-PufX from Rba. sphaeroides
- Single particle analysis by cryoElectron Microscopy of a small non symemetrical membrane protein
- 2D crystals of Light Harversting Complex, LH2, from Rba. sphaeroides
- 3D reconstruction of LH1-RC-PufX, 280 Kda, at 12 A resolution
- 3D reconstruction of LH1-RC-PufX, 280 kDa, at 12 A resolution
- 2D crystals of Light Harversting Complex, LH2, from Rba. sphaeroides
- schematic model of the coupling between the non equivalent catalytic sites of ABC transporters
- schematic model of the coupling between the non equivalent catalytic sites of ABC transporters
- schematic model of the coupling between the equivalent catalytic sites of ABC transporters
- Tubular to planar membranes upon conformational changes of BmrA, a ABC transporter
- Orientation of the Shiga toxin B subunit toward the membrane
- Pores in lipid membrane
- Functionalyzed tubes made of cerebroside lipids
- Polymersomes
- Light sensitive Polymersomes
- Tubular to planar membrane transition mediated by transmembrane protein
- Biocompatible gold nanorods for cancer research
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- Liposome with actin cortex aspirated in a micropipet
- Actin filled liposomes form a cortex if polymerization is activated at the membrane
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- Symmetry breaking of the actin gel around a bead
- C. elegans embryo during ventral closure
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- S2 RNA regulatory module
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fig1
Capture et analyse de cellules tumorales circulantes.
Encadré du haut : représentation de la technologie que nous avons développée pour capturer et étudier les cellules tumorales. Un réseau de colonnes formées de particules magnétiques portant des anticorps dirigés contre les cellules d'intérêt sont auto-assemblés sous un champ magnétique dans un canal microfluidique. L'échantillon (par exemple, un prélèvement sanguin de patient) est envoyé dans le canal. Les cellules portant les antigènes de surface appropriés (rouges et bleues) sont retenues, alors que les cellules négatives (bleues) ne le sont pas. Les cellules capturées peuvent alors être marquées avec différents biomarqueurs, puis observées et étudiées avec grande précision. Encadré du bas : Image des cellules cancéreuses d'un patient atteint d'un lymphome, obtenue par microscopie confocale in situ après la récupération. Les cellules comportent de multiples immunomarquages (anticorps verts, jaunes et rouges, et marqueur de l'ADN bleu).