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Carbohydrate-modified interfaces have been shown to be valuable tools for the study of protein–glycan recognition events. Label-free approache such as plasmonic based techniques are particularly attractive. This paper describes a new analytical platform for the sensitive and selective screening of carbohydrate–lectin interactions using plasmon waveguide resonance. Planar optical waveguides (POW), consisting of glass prisms coated with silver (50 nm) and silica (460 nm) layers were derivatized with mannose or lactose moieties. The specific association of the resulting interface with selected lectins was assessed by following the changes in its plasmonic response. The immobilization strategy investigated in this work is based on the formation of a covalent bond between propargyl-functionalized glycans and surface-linked azide groups via a Cu(I) “click” chemistry. Optimization of the surface architecture through the introduction of an oligo(ethylene glycol) spacer between the plasmonic surface and the glycan ligands provided an interface which allowed screening of glycan–lectin interactions in a highly selective manner. The limit of detection (LOD) of this method for this particular application was found to be in the subnanomolar range (0.5 nM), showing it to constitute a promising analytical platform for future development and use in a pharmaceutical or biomedical setting.

6 pages; International audience; We report a preliminary study of two novel complexes combining a paramagnetic transition metal (Cu(II)) and a cyclophane-type TTF-bipyridine ligand TTF-bipy = (cis)2,7-bis(pentylsulfanyl)-3,6- [2,2-bipyridine-bis(4,4-methanediyl)bis-sulfanyl]tetrathiafulvalene. The syntheses of the complexes Cu(hfac)2(TTF-bipy) (hfac = hexafluoroacetylacetonate) and Cu(NO3)2(TTF-bipy)·H2O are reported. The results of single-crystal EPR measurements are discussed on the basis of structural features deduced from preliminary X-ray diffraction data and indicate that these neutral molecular complexes behave as isolated paramagnetic units.

12 pages; International audience; Three heterobimetallic MnIIIFeII complexes: [Mn(5-Br-salpn)(H2O)]2[Fe(CN)5NO]2H2O (1), [{Mn(salen)}2Fe(CN)5NO]2H2O (2) and [{Mn(saltmen)}4Fe(CN)5NO](ClO4)2H2O2CH3OH (3), have been synthesized by the reactions of MnIII/Schiff–base (SB) complexes, [Mn(SB)(H2O)]+, (SB being salen2 =N,N0-ethylenebis(salicylideneiminato) dianion; 5-Br-salpn2 = N,N0-1,3-propylenebis(5-bromosalicylideneiminato) dianion or saltmen2 = N,N0-(1,1,2,2-tetramethylethylene) bis(salicylideneiminato) dianion) with the [Fe(CN)5NO]2building block. X-Ray diffraction analyses on single crystals reveal that 1 has a trinuclear molecular structure, 2 displays a two-dimensional (2D) network structure, and 3 possesses a new 2D network of MnIII dinuclear motifs. The magnetic measurements show that the interaction between the MnIII S = 2 spins through the [NRC–Fe–CRN] bridges is systematically of antiferromagnetic nature: J/kB = 0.95(5) K and J/kB = 1.15(5) K for 1 and 2, respectively, while the direct MnIII–MnIII interaction, in the {Mn2(saltmen)2} dinuclear units present in 3, is ferromagnetic with J/kB = +1.75(5) K. Due to the ST = 4 spin ground state of these dinuclear units and the uniaxial magnetic anisotropy brought by the Mn(III) metal ions, 3 exhibits singlemolecule magnet properties. The 400–900 nm optical properties of the three compounds have been also investigated, showing no significant photoactivity unlike in the Na2[Fe(CN)5NO precursor

9 pages; International audience; Background: Proteolysis, involved in many processes in living organisms, is tightly regulated in space and time under physiological conditions. However deregulation can occur with local persistent proteolytic activities, e.g. in inflammation, cystic fibrosis, tumors, or pancreatitis. Furthermore, little is known about the role of many proteases, hence there is a need of new imaging methods to visualize specifically normal or disease-related proteolysis in intact bodies. Methodology/Principal Findings: In this paper, a new concept for non invasive proteolysis imaging is proposed. Overhauser-enhanced Magnetic Resonance Imaging (OMRI) at 0.2 Tesla was used to monitor the enzymatic hydrolysis of a nitroxide-labeled protein. In vitro, image intensity switched from 1 to 25 upon proteolysis due to the associated decrease in the motional correlation time of the substrate. The OMRI experimental device used in this study is consistent with protease imaging in mice at 0.2 T without significant heating. Simulations show that this enzymatic-driven OMRI signal switch can be obtained at lower frequencies suitable for larger animals or humans. Conclusions/Significance: The method is highly sensitive and makes possible proteolysis imaging in three dimensions with a good spatial resolution. Any protease could be targeted specifically through the use of taylor-made cleavable macromolecules. At short term OMRI of proteolysis may be applied to basic research as well as to evaluate therapeutic treatments in small animal models of experimental diseases.

International audience; Reported herein are the synthesis, structural and magnetic characterisation of a dinuclear FeII triple helicate that displays an unprecedented reversible asymmetric high spin to low spin crossover characterised by a thermal hysteresis: indeed the high spin state can be recovered by white light irradiation at 10 K.

International audience; A soluble molecular analogue of photoresponsive Co/Fe Prussian blues is described within this report. As judged via a variety of spectroscopic, magnetic, and crystallographic methods, electron transfer within the octanuclear complex (below 250 K) converts paramagnetic red crystals into green diamagnetic ones. The color and magnetic changes are associated with the transformation of FeIIILS-CN-CoIIHS units into FeIILS-CN-CoIIILS fragments in manner that is identical to that found for the An[Co(OH2)(6-6m)][Fe(CN)6]m·xH2O (An = alkali metal cation) family of three-dimensional Prussian blues. Moreover, this intramolecular electron transfer can be quantitatively circumvented via rapid thermal quenching and reversed via simple white light irradiation at low temperatures. Remarkably the data suggests that thermally or photoinduced paramagnetic metastable phases are identical and exhibit long relaxation times that approach 10 years at 120 K.

International audience; 3-Methoxy-17α-ethynylestradiol or mestranol is a prodrug for ethynylestradiol and the estrogen component of some oral contraceptive formulations. We demonstrate here that a single core multimodal probe for imaging - SCoMPI - can be efficiently grafted onto mestranol allowing its tracking in two breast cancer cell lines, MDA-MB-231 and MCF-7 fixed cells. Correlative imaging studies based on luminescence (synchrotron UV spectromicroscopy, wide field and confocal fluorescence microscopies) and vibrational (AFMIR, synchrotron FTIR spectromicroscopy, synchrotron-based multiple beam FTIR imaging, confocal Raman microspectroscopy) spectroscopies were consistent with one another and showed a Golgi apparatus distribution of the SCoMPI-mestranol conjugate in both cell lines.