Synthesis and Characterization of Magnetic Superadsorbent Fe3O4-PEG-Mg-Al-LDH Nanocomposites for Ultrahigh Removal of Organic Dyes.

Considering the huge demands for economical and reliable eco-remediation applications, the goal of the present work is to synthesize cost-effective and functionally efficient magnetic layered nanocomposite adsorbents for the effective adsorption of dyes followed by easy separation from wastewater. This would ensure good reusability of adsorbents without altering its adsorption capacity in a relatively short time manner. To achieve this, different molecular weights of polyethylene glycol (PEG)-modified Fe3O4 combined with Mg-Al-layered double hydroxides (MAN-LDH) were synthesized and characterized using powder X-ray diffraction, Fourier transform infrared, scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, differential thermal analysis, energy-dispersive X-ray, and inductively coupled plasma optical emission spectroscopy. The efficacy of various adsorption parameters for the removal of methyl orange (MO) from water using Fe3O4-PEG-Mg-Al-LDH (FPL) adsorbents with different molecular weights of PEG (2FPL, 4FPL, and 6FPL) were investigated, and the results were compared. The maximum adsorption capacities of 2FPL, 4FPL, and 6FPL for MO were found to be 775.19, 826.44, and 833.33 mg/g, respectively. Detailed adsorption studies confirm that the higher adsorption capacity of 6FPL is due to the fast exchange of anions (NO3 -) by MO in the interlayers of MAN-LDH, larger surface area, hydrogen bonding, and electrostatic interaction between adsorbate and adsorbent. The thermodynamic data indicate that the adsorption behavior is spontaneous and endothermic in nature. The reusability of all FPL adsorbents is observed to be excellent. The MAN-LDH recoated after the 31st-cycle nanocomposites show a recovery of 100% adsorption efficiency, similar to the freshly prepared 6FPL. Such systematic studies greatly help in advancing the applications of newly functionalized nanomaterials toward eco-remediation approaches.

Modulating the structure of EGFR with UV light: new possibilities in cancer therapy.

The epidermal growth factor receptor (EGFR) is a member of the ErbB family of receptor tyrosine kinases. EGFR is activated upon binding to e.g. epidermal growth factor (EGF), leading to cell survival, proliferation and migration. EGFR overactivation is associated with tumor progression. We have previously shown that low dose UVB illumination of cancer cells overexpressing EGFR prior to adding EGF halted the EGFR signaling pathway. We here show that UVB illumination of the extracellular domain of EGFR (sEGFR) induces protein conformational changes, disulphide bridge breakage and formation of tryptophan and tyrosine photoproducts such as dityrosine, N-formylkynurenine and kynurenine. Fluorescence spectroscopy, circular dichroism and thermal studies confirm the occurrence of conformational changes. An immunoassay has confirmed that UVB light induces structural changes in the EGF binding site. A monoclonal antibody which competes with EGF for binding sEGFR was used. We report clear evidence that UVB light induces structural changes in EGFR that impairs the correct binding of an EGFR specific antibody that competes with EGF for binding EGFR, confirming that the 3D structure of the EGFR binding domain suffered conformational changes upon UV illumination. The irradiance used is in the same order of magnitude as the integrated intensity in the solar UVB range. The new photonic technology disables a key receptor and is most likely applicable to the treatment of various types of cancer, alone or in combination with other therapies.

Sub-picometer structural information of graphene hidden in a 50 pm resolved image.

In a 2D self-organized crystalline structure more than 1000 unit-cells can be observed in a single image. Here we exploit the benefits from having a large number of observations of the same unit cell utilizing an image processing methodology. We obtain sub-picometer resolution data from a 50 pm image of graphene, revealing a 1% axial elongation and a 3 fold symmetry, indicating a chair conformation.

Photonic immobilization of BSA for nanobiomedical applications: creation of high density microarrays and superparamagnetic bioconjugates.

Light assisted molecular immobilization has been used for the first time to engineer covalent bioconjugates of superparamagnetic nanoparticles and proteins. The technology involves disulfide bridge disruption upon UV excitation of nearby aromatic residues. The close spatial proximity of aromatic residues and disulfide bridges is a conserved structural feature in proteins. The created thiol groups bind thiol reactive surfaces leading to oriented covalent protein immobilization. We have immobilized a model carrier protein, bovine serum albumin, onto Fe(3)O(4)@Au core-shell nanoparticles as well as arrayed it onto optically flat thiol reactive surfaces. This new immobilization technology allows for ultra high dense packing of different bio-molecules on a surface, allowing the creation of multi-potent functionalized active new biosensor materials, biomarkers identification and the development of nanoparticles based novel drug delivery system.

Towards nanoscale biomedical devices in medicine: biofunctional and spectroscopic characterization of superparamagnetic nanoparticles.

Medical interest in nanotechnology originates from a belief that nanoscale therapeutic devices can be constructed and directed towards its target inside the human body. Such nanodevices can be engineered by coupling superparamagnetic nanoparticle to biomedically active proteins. We hereby report the immobilization of a PhEst, a S-formylglutathione hydrolase from the psychrophilic P. haloplanktis TAC125 onto the gold coated surface of modified superparamagnetic core-shell nanoparticles (Fe(3)O(4)@Au). The synthesis of the nanoparticles is also reported. S-formylglutathione hydrolases constitute a family of ubiquitous enzymes which play a key role in formaldehyde detoxification both in prokaryotes and eukaryotes. PhEst was originally annotated as a putative feruloyl esterase, an enzyme that releases ferulic acid (an antioxidant reactive towards free radicals such as reactive oxygen species) from polysaccharides esters. Dynamic light scattering, scanning electron microscopy with energy dispersive X-ray spectroscopy, UV-visible absorption spectroscopy, fluorescence spectroscopy, magnetic separation technique and enzyme catalytic assay confirmed the chemical composition of the gold covered superparamagnetic nanoparticles, the binding and activity of the enzyme onto the nanoparticles. Activity data in U/ml confirmed that the immobilized enzyme is approximately 2 times more active than the free enzyme in solution. Such particles can be directed with external magnetic fields for bio-separation and focused towards a medical target for therapeutical as well as bio-sensor applications.