Rhodopsin reconstituted into a planar-supported lipid bilayer retains photoactivity after cross-linking polymerization of lipid monomers

Transmembrane proteins (TMPs), particularly ion channels and receptors, play key roles in transport and signal transduction. Many of these proteins are pharmacologically important and therefore targets for drug discovery. TMPs can be reconstituted in planar-supported lipid bilayers (PSLBs), which has led to development of TMP-based biosensors and biochips. However, PSLBs composed of natural lipids lack the high stability desired for many technological applications. One strategy is to use synthetic lipid monomers that can be polymerized to form robust bilayers. A key question is how lipid polymerization affects TMP structure and activity. In this study, we have examined the effects of UV polymerization of bis-Sorbylphosphatidylcholine (bis-SorbPC) on the photoactivation of reconstituted bovine rhodopsin (Rho), a model G-protein-coupled receptor. Plasmon-waveguide resonance spectroscopy (PWR) was used to compare the degree of Rho incorporation and activation in fluid and poly(lipid) PSLBs. The results show that reconstitution of Rho into a supported lipid bilayer composed only of bis-SorbPC, followed by photoinduced lipid cross-linking, does not measurably diminish protein function.     

Ferromagnetic ordering and metamagnetism in malonate bridged 3D diamond-like and honeycomb-like networks: [Cu(mal)(DMF)]n and [[Cu(mal)(0.5pyz)].H2O]n (mal = Malonate Dianion,DMF = N,N-dimethylformamide,pyz = Pyrazine)

Two three-dimensional (3D) malonate bridged networks, [Cu(mal)(DMF)](n) (1) and [[Cu(mal)(0.5pyz)].H(2)O](n) (2), have been synthesized in H(2)O-DMF solution. Compound 1 exhibits ferromagnetic ordering below 2.6 K (T(c)), and 2 displays a metamagnetic behavior below 3.2 K (T(N)).     

Raman study NH4Cl near the tricritical point

The Raman spectrum of NH₄Cl has been studied as a function of temperature and pressure close to the multicritical point at which the λ-transition changes from first to second order. Variations in the intensities of appropriate bands have been used to calculate the critical exponents for the order parameter. By varying the temperature at fixed pressures of zero, 3.0 k bar and 1.5 k bar, exponent values of β = 0.154 ± 0.012, β = 0.33 ± 0.06 and β = 0.26 ± 0.06 have been obtained for the first-order, second-order and multicritical regions respectively.Our first-order exponent value is close to that observed by previous workers, our second-order value is close to that predicted by the three dimensional Ising model, and our multicritical value is close to that predicted by mean field theory.     

The interaction of sodium caseinate with monoglyceride and diglyceride at the oil-water interface in corn oil-in-water emulsions and its effect on emulsion stability

The slow rate of drop coalescence at 5 C in concentrated corn oil-in-water emulsions stabilised with sodium caseinate, glyceryl monostearate and glyceryl distearate was deduced from changes in the drop size distribution. Both pH and the monoglyceride/diglyceride ratio influenced coalescence. At any pH minimum coalescence was observed at a 5/2 monoglyceride/diglyceride ratio. This was attributed to association of caseinate with a previously formed complex of monoglyceride and diglyceride, so supporting an interpretation previously proposed on the basis of rheological data for the emulsions and for films of caseinate-glycerides at the oil-water interface.     

Photochemistry of 2,2-Dimethyl-2H-Furo[3,4-b]Pyran-4,7(3H, 5H)-Dione

Irradiation (λ > 340 nm) of the title compound 2a in t-BuOH affords 3,3,10,10-tetramethyl-2,8-dioxatricyclo-[4.3.2.0^1,6]undecane-5,9-dione (3) via photoextrusion of 2-methylpropene and subsequent photocycloaddition of 2a to the alkene. The same regioisomer 3 is formed selectively and in much higher yields on irradiating 2a in the presence of excess 2-methylpropene. Irradiation of 3 (λ = 300 nm) in t-BuOH in the presence of the same alkene gives a 6:1 mixture of spirooxetanes 7a and 7b but not α-cleavage products. In 2-propanol, 2a is photoreduced to a 2:1 mixture of diastereoisomeric hydrodimers 9 .     

Laser-Printed Plasmonic Metasurface Supporting Bound States in the Continuum Enhances and Shapes Infrared Spontaneous Emission of Coupled HgTe Quantum Dots

In order to advance the development of quantum emitter-based devices, it is essential to enhance light-matter interactions through coupling between semiconductor quantum dots with high quality factor resonators. Here, efficient tuning of the emission properties of HgTe quantum dots in the infrared spectral region is demonstrated by coupling them to a plasmonic metasurface that supports bound states in the continuum. The plasmonic metasurface, composed of an array of gold nanobumps, is fabricated using single-step direct laser printing, opening up new opportunities for creating exclusive 3D plasmonic nanostructures and advanced photonic devices in the infrared region. A 12-fold enhancement of the photoluminescence in the 900–1700 nm range is observed under optimal coupling conditions. By tuning the geometry of the plasmonic arrays, controllable shaping of the emission spectra is achieved, selectively enhancing specific wavelength ranges across the emission spectrum. The observed enhancement and shaping of the emission are attributed to the Purcell effect, as corroborated by systematic measurements of radiative lifetimes and optical simulations based on the numerical solution of Maxwell's equations. Moreover, coupling of the HgTe photoluminescence to high quality factor modes of the metasurface improves emission directivity, concentrating output within an ≈20° angle.