Magnetic hydrophobic affinity nanobeads for lysozyme separation

N-Methacryloyl-l-phenylalanine (MAPA) containing poly(2-hydroxyethylmethacrylate) based magnetic [mag-poly(HEMA–MAPA)] nanobeads was prepared for lysozyme purification form chicken egg white. MAPA was synthesized by reacting methacryloyl chloride with l-phenylalanine methyl ester and provided hydrophobic functionality to the nanobeads. Size of mag-poly(HEMA–MAPA) nanobeads was 386 nm and obtained by surfactant free emulsion polymerization of HEMA and MAPA having a specific surface area of 580 m²/g. Mag-poly(HEMA–MAPA) nanobeads were characterized by FTIR, AFM, TEM, ESR, and elemental analysis. Lysozyme adsorption experiments were investigated under different conditions in batch system (i.e., medium pH, protein concentration, temperature, salt type). Lysozyme adsorption capacity of mag-poly(HEMA) and mag-poly(HEMA–MAPA) nanobeads from aqueous solutions was estimated as 24 and 517 mg/g, respectively. Lysozyme molecules were desorbed with 50% ethylene glycol solution with 98% recovery. It was observed that mag-poly(HEMA–MAPA) nanobeads can be used without significant decrease in lysozyme adsorption capacity after ten adsorption–desorption cycles. Mag-poly(HEMA–MAPA) nanobeads was used for the purification of lysozyme from chicken egg white. Purity of lysozyme was estimated by SDS-PAGE.     

Classical force field parameters for two high-affinity ligands of FKBP12

FKBP12 is an important target in the treatment of transplant rejection and is also a promising target for cancer and neurodegenerative diseases. We determined for two ligands of nanomolar affinity the set of parameters in the CHARMM force field. The fitting procedure was based on reproducing the quantum chemistry data (distances, angles, and energies). Since the dynamical behavior of such ligands strongly depends on the dihedral angles, care was taken to derive the corresponding parameters. Moreover, since each of the central core region of these two ligands is similar to other known ligands or drugs of other proteins, part at least of these parameters could also be useful for these other ligands.     

Structural diversity and solution behavior of low-valent iridium complexes bearing 1,4-diazabutadiene ligands

Three types of 1,4-diazabutadiene stabilized low-valent iridium complexes, namely [IrCl(cod)(MesDAB)] (1), [IrCl(coe)(MesDAB)] (2) and [IrCl(MesDAB)₂] (3), have been prepared from 1,4-bis(2,4,6-trimethylphenyl)-1,4-diaza-1,3-butadiene (MesDAB) and [IrCl(cod)]₂ or [IrCl(coe)₂]₂, respectively. The complexes have been investigated by NMR spectroscopy and X-ray diffraction experiments. While tetra-coordinated 2 and penta-coordinated 3 maintain their solid state structure in solution, penta-coordinated 1 shows fluxional behavior. The crystal structures determined indicate strong π-backbonding towards the MesDAB ligand in all cases.     

锡的热液配合体系的理论热力学模型

根据锡的最新热力学资料和热液锡矿化作用的地球化学特性,理论模拟了热液配合体系中,温度、pH值、氧逸度、氟和氯的浓度对锡的迁移形式、稳定性及其溶解度的控制机理,指出了锡沉淀富集的最佳途径。     

Identification, characterization, and physiological actions of factor H as an adrenomedullin binding protein present in human plasma

A recently discovered adrenomedullin binding protein has been characterized as complement factor H, an important regulator of the complement cascade. This review will describe the evidence that led to the identification of factor H as an adrenomedullin binding protein and will address the implications that such binding has in the radioimmunoassay of AM in plasma. We will also describe the possible physiological implications of AM binding: namely, factor H suppresses the antimicrobial activity of AM, enhances AM-mediated induction of cyclic-AMP in rat fibroblasts, and augments the AM-mediated growth of a human cancer cell line. These initial studies suggest that factor H may be an important factor in the regulation of AM physiology. The elucidation of the mechanisms that modulate AM activity will be necessary for the understanding of the role of AM in normal and pathological conditions.