Magnetic field effects on coherent backscattering of light

We have studied the influence of magneto-optical Faraday rotation on coherent backscattering of light experimentally, theoretically and by computer simulations of Monte-Carlo type. The consistency of these three approaches reveals new aspects of the propagation of vector waves in turbid media with and without Faraday rotation. Experimentally, we have demonstrated that the Faraday rotation may almost completely destroy the reciprocity of light paths. However, as shown by the simulations, the cone of coherent backscattering may not only be destroyed but also shifted off the exact backscattering direction, parallel to the magnetic field, as long as the amount of circular polarization is not completely destroyed by the multiple scattering. The relationship between coherent backscattering, depolarization and Faraday rotation are explained by a simple path model of vector waves. This leads to a new characteristic correlation length required to properly describe the influence of Faraday rotation on multiple light scattering. Received 28 January 2000     

Experimental realization of a model glass former in 2D

We have studied binary two-dimensional (2D) mixtures of superparamagnetic colloidal particles interacting through magnetic dipole moments, which were induced by an external magnetic field B. By tuning B the effective system temperature could be widely adjusted. Time-dependent particle coordinates measured by video-microscopy provide radial pair-distribution functions, mean-square displacements as well as evidence for heterogeneous dynamics. Characteristic features of 3D glass formers are observed experimentally in 2D for the first time.     

Velocity of high frequency sound waves in oriented DNA fibres and films determined by Brillouin scattering

Summary We have measured the velocity of acoustic microwave phonons in fibres and films of oriented DNA. The sound velocity is found to be surprisingly isotropic and to decrease substantially during hydration of DNA. No optical modes have been detected in the frequency range covered from 5 to 120 GHz. The photoelastic constants are strongly anisotropic.

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Zusammenfassung Wir haben die Geschwindigkeit akustischer Mikrowellenphononen in Fasern und Filmen orientierter DNS bestimmt. Die Schallgeschwindigkeit ist überraschend isotrop und nimmt mit steigender DNS-Hydration wesentlich ab. Im Frequenzbereich zwischen 5 und 120 GHz konnten keine optischen Moden nachgewiesen werden. Die photoelastischen Konstanten sind stark anisotrop.

     

Elastic behavior of a two-dimensional crystal near melting

Using positional data from video microscopy, we determine the elastic moduli of two-dimensional colloidal crystals as a function of temperature. The moduli are extracted from the wave-vector-dependent normal-mode spring constants in the limit q-->0 and are compared to the renormalized Young's modulus of the Kosterlitz-Thouless-Halperin-Nelson-Young theory. An essential element of this theory is the universal prediction that Young's modulus must approach 16 pi at the melting temperature. This is indeed observed in our experiment.     

Gas chromatography–mass spectroscopy optimization by computer simulation,application to the analysis of 93 volatile organic compounds in workplace ambient air

GC–MS optimization method including both advantages from chromatographic separation and mass spectrometric detection was designed for a set of 93 volatile organic compounds. Only a few experiments were necessary to determine the thermodynamic retention parameters for all compounds on a RTX-VMS column. From these data, computer simulation was used in order to predict the retention times of the compounds in temperature programmed gas chromatography. Then, an automatic selection of ions from the NIST database was performed and compared to the optimum conditions (full separation of VOC). This simulation-selection procedure was used to screen a numerous set of GC and MS conditions in order to quickly design a GC–MS method whatever the set of compounds considered.     

Chiral nematic suspensions of cellulose crystallites; phase separation and magnetic field orientation

Suspensions of rod-like cellulose crystallites of axial ratio ≈ 20-40, prepared by acid hydrolysis of natural cellulose fibres with sulphuric acid, give stable ordered fluids that display well-formed textures and disclinations characteristic of chiral nematic liquid crystalline phases. The critical volume fraction for phase separation of salt-free suspensions is typically 0.03, with a relatively narrow biphasic region. Because of the negative diamagnetic susceptibility of cellulose, the ordered phase becomes oriented in a magnetic field with its chiral nematic axis parallel to the applied field.     

Partial oxidation and oxidative polymerization of metallothionein

One mechanism for regulation of metal binding to metallothionein (MT) involves the non-enzymatic or enzymatic oxidation of its thiols to disulfides. Formation and speciation of oxidized MT have not been investigated in detail despite the biological significance of this redox biochemistry. While metal ion-bound thiols in MT are rather resistant towards oxidation, free thiols are readily oxidized. MT can be partially oxidized to a state in which some of its thiols remain reduced and bound to metal ions. Analysis of the oxidation products with SDS-PAGE and a thiol-specific labeling technique, employing eosin-5-iodoacetamide, demonstrates higher-order aggregates of MT with intermolecular disulfide linkages. The polymerization follows either non-enzymatic or enzymatic oxidation, indicating that it is a general property of oxidized MT. Supramolecular assemblies of MT add new perspectives to the complex redox and metal equilibria of this protein.     

Dual nanomolar and picomolar Zn(II) binding properties of metallothionein

Each of the seven Zn(II) ions in the Zn(3)S(9) and Zn(4)S(11) clusters of human metallothionein is in a tetrathiolate coordination environment. Yet analysis of Zn(II) association with thionein, the apoprotein, and analysis of Zn(II) dissociation from metallothionein using the fluorescent chelating agents FluoZin-3 and RhodZin-3 reveal at least three classes of sites with affinities that differ by 4 orders of magnitude. Four Zn(II) ions are bound with an apparent average log K of 11.8, and with the methods employed, their binding is indistinguishable. This binding property makes thionein a strong chelating agent. One Zn(II) ion is relatively weakly bound, with a log K of 7.7, making metallothionein a zinc donor in the absence of thionein. The binding data demonstrate that Zn(II) binds with at least four species: Zn(4)T, Zn(5)T, Zn(6)T, and Zn(7)T. Zn(5)T and Zn(6)T bind Zn(II) with a log K of approximately 10 and are the predominant species at micromolar concentrations of metallothionein in cells. Central to the function of the protein is the reactivity of its cysteine side chains in the absence and presence of Zn(II). Chelating agents, such as physiological ligands with moderate affinities for Zn(II), cause dissociation of Zn(II) ions from metallothionein at pH 7.4 (Zn(7)T <==> Zn(7-n)T + nZn(2+)), thereby affecting the reactivity of its thiols. Thus, the rate of thiol oxidation increases in the presence of Zn(II) acceptors but decreases if more free Zn(II) becomes available. Thionein is such an acceptor. It regulates the reactivity and availability of free Zn(II) from metallothionein. At thionein/metallothionein ratios > 0.75, free Zn(II) ions are below a pZn (-log[Zn(2+)](free)) of 11.8, and at ratios < 0.75, relatively large fluctuations of free Zn(II) ions are possible (pZn between 7 and 11). These chemical characteristics match cellular requirements for Zn(II) and suggest how the molecular structures and redox chemistries of metallothionein and thionein determine Zn(II) availability for biological processes.