Green functions of interacting systems in the strongly localized regime.

We have developed an approach to calculate the single-particle Green function of a one-dimensional many-body system in the strongly localized limit at zero temperature. Our approach sums the contributions of all possible forward scattering paths in configuration space. We demonstrate that for fermions and nearest neighbors interactions the Green function factorizes at every link connecting two sites with the same occupation. As a consequence, the conductance distribution function for interacting systems is log-normal, in the same universality class as non-interacting systems. We have developed a numerical procedure to calculate the ground state and the Green function, generating all possible paths in configuration space. Our results agree with results obtained by exact diagonalization of small systems in the limit of large disorder.

[The annexin 5 in serums of pregnant women and patients with particular types of cancer].

The detection of biomarkers to be applied to reveal different types of tumors is an actual demand of today. Since course of this disease can be asymptomatic these kinds of markers can be applied in widely-distributed screening procedures. Many types of biomarkers for detection of cancer exist. However all these markers are specific only for particular type of tumor and have no use in screening procedures for detection of this pathology. The Annexin 5, a Ca-depended phospholipid binding protein, was discovered in serums of all pregnant women on various stages of pregnancy. The study was implemented using method of latex agglutination. More than that, this protein was detected in serums of patients with several types of cancer. The possibility to apply annexin 5 as marker for screening of various types of cancer is considered.

Fluctuations of the correlation dimension at metal-insulator transitions.

We investigate numerically the inverse participation ratio, P(2), of the 3D Anderson model and of the power-law random banded matrix (PRBM) model at criticality. We found that the variance of lnP(2) scales with system size L as sigma(2)(L) = sigma(2)(infinity)-AL(-D(2)/2d), with D(2) being the correlation dimension and d the system dimension. Therefore the concept of a correlation dimension is well defined in the two models considered. The 3D Anderson transition and the PRBM transition for b = 0.3 (see the text for the definition of b) are fairly similar with respect to all critical magnitudes studied.

Anomalously large critical regions in power-law random matrix ensembles.

We investigate numerically the power-law random matrix ensembles. Wave functions are fractal up to a characteristic length whose logarithm diverges asymmetrically with different exponents, 1 in the localized phase and 0.5 in the extended phase. The characteristic length is so anomalously large that for macroscopic samples there exists a finite critical region, in which this length is larger than the system size. The Green's functions decrease with distance as a power law with an exponent related to the correlation dimension.

[Polystyrene latexes in agglutination tests: preparation and sensibilization]. / Polistirol'nye lateksy v reaktsiiakh aggliutinatsii, prigotovlenie i sensibilizatsiia.

A method for preparing polystyrene latexes for slide agglutination test is described. The latexes were used for preparing latex slide tests for evaluating C-reactive protein and myoglobin. Effects of such factors as pH, temperature, antibody concentration, and latex particles concentration, on sensitization and agglutination have been studied. The proposed approaches allow detection of the antigen in a concentration of less than 200 micrograms/liter for myoglobin and less than 8 mg/liter for C-reactive protein.

[Flavin-containing polyaminooxidase in the liver: spectral properties and localization]. / Flavinsoderzhashchaia poliaminooksidaza pecheni: spektral'nye svoistva i lokalizatsiia.

Some properties of flavin-containing polyamine oxidase from bovine liver have been studied. Limited proteolysis of the enzyme by trypsin resulted in two fragments with molecular masses of 48 and 5-8 kDa. The antigenic determinants of the protein appear to be bound to the larger proteolytic fragment. The effect of proteolysis on optical properties of the enzyme has been established. Data from immunological analysis suggest that the soluble fraction of the liver is a rich source of the enzyme.

[Purification of flavin-containing liver polyamine oxidase and luminescent properties of the ferment]. / Ochistka flavinsoderzhashchei poliaminooksidazy iz pecheni i liuminestsentnye svoistva fermenta.

A flavin-containing polyamine oxidase was isolated in an electrophoretically homogeneous state from cattle liver cytosol. The molecular mass, subunit composition and flavin content of the enzyme were determined; flavin, was shown to be covalently bound to the protein fragment of the polyamine oxidase molecule. Some optical and luminescent properties of the native and denatured enzyme were investigated. Denaturation and quenching were found to affect the luminescent properties of polyamine oxidase.

[Localization of tryptophan residues in NADPH-adrenodoxin reductase with respect to the NADPH-binding center]. / Lokalizatsiia ostatkov triptofana v NADPH-adrenodoksin reduktaze otnositel'no NADPH-sviazyvaiushchego tsentra.

It was demonstrated that the NADPH-adrenodoxin reductase molecule contains ten tryptophan residues titrated by N-bromosuccinimide. The effectiveness of the non-radiant energy transfer was used to calculate the average distance between the NADPH-binding site of the enzyme and tryptophan residues at different steps of N-bromosuccinimide-induced modification.

[Luminescent properties of NADPH: adrenodoxin reductase]. / Liuminestsentnye svoistva NADPH: adrenodoksin reduktazy.

The fluorescent and phosphorescent properties of NADPH-adrenodoxin reductase were investigated. It was shown that the fluorescence of protein tryptophanyls was quenched completely by acrylamide and partially by ionic quenchers (I- and Cs+). A removal of the prosthetic group from the protein causes insignificant changes in fluorescent properties of the enzyme. The denaturation of the enzyme by urea was accompanied by growth of quenching parameters. Indeed, some differences were observed in the quenching of flavin fluorescence by ionic quenchers (I- and Cs+). NADPH appeared to be an efficient quencher of NADPH-adrenodoxin reductase tryptophan fluorescence. Using Förster's equations for non-radiative energy transfer, the distance between NADPH-binding site and tryptophanyls was evaluated to 35-40 A.