Gender difference regarding selenium penetration into the mouse brain

A sex difference in the penetration of selenium into the brain was observed using lipopolysaccharide (LPS)-injected mice. The selenium concentration increased in the brains of sodium selenite-injected LPS-treated female mice, but not males. The selenium concentration peaked when selenite was injected 3 h after the injection of LPS into female mice. In addition, selenium in the brain increased when a dosage of 30 μmol/kg and more of selenite was injected into LPS-treated female mice. Also, the selenium concentration in the brain increased and peaked 2–3 h after selenite injection; 24 h later, the level was similar to the Se-only group. The penetration of selenium into the brain was inhibited by pretreatment with aminoguanidine, an inhibitor of nitric oxide synthetase. From the present results, selenium more easily penetrated into the brains of female mice compared to males after LPS treatment, and nitric oxide may have affected the penetration. However, the sex difference mechanism for selenium penetration needs further investigation.     

Protein molecular dynamics with electrostatic force entirely determined by a single Poisson-Boltzmann calculation

The electrostatic force including the intramolecular Coulombic interactions and the electrostatic contribution of solvation effect were entirely calculated by using the finite difference Poisson-Boltzmann method (FDPB), which was incorporated into the GROMOS96 force field to complete a new finite difference stochastic dynamics procedure (FDSD). Simulations were performed on an insulin dimer. Different relative dielectric constants were successively assigned to the protein interior; a value of 17 was selected as optimal for our system. The simulation data were analyzed and compared with those obtained from 500-ps molecular dynamics (MD) simulation with explicit water and a 500-ps conventional stochastic dynamics (SD) simulation without the mean solvent force. The results indicate that the FDSD method with GROMOS96 force field is suitable to study the dynamics and structure of proteins in solution if used with the optimal protein dielectric constant.     

Arteriovenous carboxyhemoglobin difference in critical illness: fiction or fact?

It is still unclear whether the paradoxical arteriovenous carboxyhemoglobin (COHb) difference found in critical illness is due to increased COHb production by the lung, or whether this gradient is caused by technical artifacts using spectrophotometry. In healthy and matched endotoxemic sheep, blood gases were analyzed with a standard ABL 625 and the updated version, an ABL 725. The latter one was accurately calibrated for COHb wavelengths (SAT 100) to eliminate the FCOHb dependency on oxygen tension. All endotoxemic sheep exhibited a hypotensive-hyperdynamic circulation and a pulmonary hypertension. Interestingly, arteriovenous COHb difference occurred in both healthy and endotoxemic sheep (P<0.001 each). Arterial and central venous COHb concentrations determined with the ABL 625 were significantly lower than those measured with the ABL 725 (P<0.001 each). We conclude that (a) arteriovenous COHb difference per se does not reflect critical illness and (b) measurements with an ABL 625 underestimate COHb concentrations.     

Calculation of electric fields induced in the human knee by a coil applicator

Calculations are presented of the induced electric fields and current densities in the cartilage of the knee produced by a coil applicator developed for applying pulsed magnetic fields to osteoarthritic knees. This applicator produces a sawtooth-like magnetic field waveform composed of a series of 260-micros pulses with a peak to peak magnitude of approximately 0.12 mT in the cartilage region. The simulations were performed using a recently developed 3 dimensional finite difference frequency domain technique for solving Maxwell's equations with an equivalent circuit model. The tissue model was obtained from the anatomically segmented human body model of Gandhi. The temporal peak electric field magnitude was found to be -153 mV/m, averaged within the medial cartilage of the knee for the typical dB/dt excitation levels of this coil. The technique can be extended to analyze other excitation waveforms and applicator designs.     

Carboxyl-terminal modification alters the subunit interactions and assembly pathways of normal and sickle hemoglobins

Parallel isofocusing studies established that carboxypeptidase A removal of the His-146 (HC3) and Tyr-145 (HC2) residues of heme subunits affected the assembly properties of both Des (A) and Des (S) with heme chains, albeit to differing degrees. Indeed, the rate of Des (A) oligomer dissociation (k ₁), as determined by visible spectroscopy, was 4.3-fold faster than that of its native (A) counterpart. Furthermore, Soret spectral studies have affirmed distinct rates of normal (HbA), sickle (HbS), and Des HbA hemoglobin assembly (k₂) from their and [Des (A)] heme-containing monomers. Matching kinetic analysis of Des (A) and Des (S) chain assembly (with an identical chain) revealed 4.6- and 7.8-fold faster combination rates than those seen for (A) and (S) chains, respectively. This 3-fold disparity in rates strongly supports the critical role of the -6 (A3) residue, and its amino-terminal region, in chain partner recognition and subsequent human hemoglobin assembly.     

The detection of vegetational change by multitemporal analysis of LANDSAT data: the effects of goose foraging

1 The North American mid-continent population of lesser snow geese now exceeds 3 million birds and the population is increasing in the order of 7% per annum. The foraging activities of the birds on Arctic breeding grounds are leading to loss of vegetation and habitat destruction, particularly in coastal areas bordering the Hudson and James Bays.
2 Multitemporal analysis of LANDSAT data has been carried out to detect vegetational change from 1973 to 1993 at La Pérouse Bay and its vicinity, the site of a breeding colony of snow geese.
3 Difference vegetation images (DVI) (difference between infra-red and red images) were prepared from images obtained in late summer in 1973, 1984 and 1993, in order to enhance vegetation density. Pair-wise differences were calculated between these DVI images, which resulted in three, secondary, classified images. Classification of the three secondary images (1973–84, 1984–93, 1973–93) yielded three well-defined classes: water, vegetation decline and no change in vegetation.
4 Histogram counts gave the following values for areas of vegetation decline: 1973–84, 1026 ha; 1984–93, 1428 ha; 1973–93, 2454 ha.
5 The loss of vegetation and the destruction of habitat are discussed in relation to the foraging activities of the expanding goose population.     

Gene flow and allozymic population structure in the clam Venus antiqua (King of Broderip), (Bivalvia, Veneriidae) from Southern Chile

Using horizontal electrophoresis, 13 allozyme loci were screened in 144 adult clams (Venus antiqua) (King of Broderip) from 5 geographic samples in southern Chile. Polymorphism was detected at 11 loci across the sampling localities. Gene frequency differences rather than the alternative fixation of alleles characterize these collecting sites. Direct-count heterozygosity fluctuated between 6.8% and 10.3%, with a generalized and significant heterozygote deficiency detected in every locality. Similar levels of genetic diversity were detected in both exploited banks and one presumed unmanaged population. Substantial estimates of demic structuration were found at the total population (F_ST=0.107) and regional levels (F_ST=0.143), with coinciding high inbreeding estimates (F_IS=0.57). Although no statistically significant evidence of genetic substructuring was found at the within-region comparison (F_ST=0.007), a generalized heterozygote deficiency (F_IS=0.57) also characterized that hierarchical level. Spatial correlation of gene frequencies indicated a nearly random distribution of genotypes along the latitudinal distribution of samples. The high rates of global, and the within-region rates of gene flow suggest substantial larval interchange via long-distance dispersal that prevent differentiation by drift alone. Accordingly, no discrete genetic units can be recognized for the species at any spatial scale. Apparently, high recruitment rates help in replenishing genetic variants lost by continuous overfishing, thus explaining why human extraction has not resulted in major losses of genetic variation for individual populations. The slow-growing rate and delayed sexual maturation of this clam species are apparently stronger limiting factors than human-induced genetic erosion for the conservation of natural beds and viable captive management of V. antiqua.     

The Principal Neutralizing Determinant of HIV-1IIIB: Conformation of the Peptide Bound to a Neutralizing Antibody Studied by 2D-NMR

RP135 is a 24-residue peptide corresponding to the principal neutralizing determinant of the envelope glycoprotein gp120 of the human immunodeficiency virus type 1. We have studied the conformation of RP135 in complex with a neutralizing antibody 0.5 raised against gp120 by 2D NMR spectroscopy. The antigenic determinant recognized by this antibody was mapped using a combination of HOHAHA and ROESY measurements, in which resonances of the Fab and the tightly bound peptide residues are eliminated and the mobile residues of the bound peptide are sequentially assigned. We found that residues Ser⁶ - Thr¹⁹ are part of the epitope, while Lys⁵ and Ile²⁰ are at its boundaries. Difference spectroscopy was applied to study the conformation of the bound peptide representing the epitope within the 52 kDa of the Fab complex. Specific residues of the peptide were deuterated or replaced and the difference between the NOESY spectrum of the complex with the unlabeled residue and the NOESY spectrum of the complex with the modified residue revealed the interactions of the labeled residue both within the peptide and with the Fab fragment. A total of 122 distance restraints derived from the difference spectra enabled the calculation of the structure of the bound peptide. The peptide forms a 10-residue loop, while the two segments flanking this loop interact extensively with each other and possibly form anti-parallel -strands. The loop conformation could be observed due to the unusual large size (17 residues) of the antigenic determinant recognized by 0.5.     

Crystal structure of R22L trichosanthin

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