Invariant amino acids essential for decoding function of polypeptide release factor eRF1

In eukaryotic ribosome, the N domain of polypeptide release factor eRF1 is involved in decoding stop signals in mRNAs. However, structure of the decoding site remains obscure. Here, we specifically altered the stop codon recognition pattern of human eRF1 by point mutagenesis of the invariant Glu55 and Tyr125 residues in the N domain. The 3D structure of generated eRF1 mutants was not destabilized as demonstrated by calorimetric measurements and calculated free energy perturbations. In mutants, the UAG response was most profoundly and selectively affected. Surprisingly, Glu55Arg mutant completely retained its release activity. Substitution of the aromatic ring in position 125 reduced response toward all stop codons. This result demonstrates the critical importance of Tyr125 for maintenance of the intact structure of the eRF1 decoding site. The results also suggest that Tyr125 is implicated in recognition of the 3d stop codon position and probably forms an H-bond with Glu55. The data point to a pivotal role played by the YxCxxxF motif (positions 125–131) in purine discrimination of the stop codons. We speculate that eRF1 decoding site is formed by a 3D network of amino acids side chains.     

Production and analytical properties of antibodies with high specificity to zearalenone

The time course of production, specificity, and analytical potential of anti-zearalenone polyclonal rabbit antibody synthesized by formaldehyde condensation and conjugated to bovine serum albumin were investigated. The relative cross-reactivities with natural analogues were: zearalenone, 100%; alpha-zearalenol, 0.15%; and beta-zearalenol, < 0.02%. With synthetic analogues: zearalanone, 31.7% and alpha-zearalanol, 0.12%. An enzyme immunoassay for zearalenone with a sensitivity of 0.1 ng/ml was developed on the basis of these antibodies and solid-phase conjugates homologous to the immunogen in the method of synthesis.     

Production and Analytical Properties of Antibodies with High Specificity to Zearalenone

The time course of production, specificity, and analytical potential of antizearalenone polyclonal rabbit antibody synthesized by formaldehyde condensation and conjugated to bovine serum albumin were investigated. The relative cross-reactivities with natural analogues were: zearalenone, 100%; -zearalenole, 0.15%; and -zearalenole, <0.02%. With synthetic analogues: zearalanone, 31.7% and -zearalanone, 0.12%. An enzyme immunoassay for zearalenone with a sensitivity of 0.1 ng/ml was developed on the basis of these antibodies and solid-phase conjugates homologous to the immunogen in the method of synthesis.     

Single-Cell Force Spectroscopy of Interaction of Lipopolysaccharides from <Emphasis Type="Italic">Yersinia pseudotuberculosis</Emphasis> and <Emphasis Type="Italic">Yersinia pestis</Emphasis> with J774 Macrophage Membrane Using Optical Tweezers

In order to investigate quantitatively the role of lipopolysaccharides (LPS) from outer bacterial membrane at the initial state of bacterium adhesion to a host cell membrane, a model system for single cell force spectroscopy was developed and used. The system comprised of an LPS-coated microsphere placed into optical trap and a J774 macrophage being approached the microsphere to initiate their binding and then moved back to rupture the bond. An “object shadow” phenomenon was discovered, manifested as large-scale variations of the signal of photodetector registering the trapped microsphere displacement, such variations emerging long before the actual interaction between the macrophage and microsphere. The theory and the measurements technique were developed for registration of the force required for detachment of bounded microsphere from the object investigated by means of optical tweezers under the “object shadow” conditions. Characteristic spectra of binding force between J774 macrophage and microspheres functionalized with various LPS, as well as LPS plus complementary antibodies preparations were obtained at the rate of detachment force application of 3–6 pN/s. Force spectrum characteristic of Yersinia pseudotuberculosis LPS possessing O-antigen had a maximum at ~14 pN with half-width of ~23 pN. The treatment of O-antigen with complementary antibodies resulted in transformation of this spectrum into a spectrum with maximum at ~10 pN and half-width of ~14 pN, being almost identical to the spectrum of Y. pestis LPS devoid of O-antigen, with a maximum at ~9 pN and half-width of ~13 pN. A possible mechanism of force spectra formation has been proposed under assumptions of nonspecific binding of O-antigen and probable receptor-type binding of LPS core region to the macrophage surface. The elastic modulus of macrophage envelope, as estimated using analysis of displacement of the contacting microsphere as an indenter, was ≈0.17 pN/nm.     

Temperature dependence of protein globule polarization and electron transport in preparations of photosynthetic reaction centers from Rhodopseudomonas sphaeroides

Differential "light-minus-dark" spectra were obtained for reaction center (RC) preparations cooled in the light and in the dark at 77 K. The two types of preparations were found to display different spectral features in the spectral regions 760-770, 790-810, 880-990 nm. Differences in the spectra of the two types were found to exist in preparations cooled to temperatures below 120-100 K, whereas at temperatures above 130 K such differences were not observed. The observed spectral changes may be associated with the polarization processes occurring in the RC globule. Samples cooled in the light and in the dark show different temperature dependencies of the efficiency of electron transfer to the secondary quinone acceptor. The differences are irreversible after cooling to temperatures below 170 K, and reversible after cooling to 180-200 K. It is postulated that the observed kinetic changes are reflections of changes in the configuration of the acceptor complex of the RC. The possible existence of a correlation between the polarization processes in the protein globule and the structural configurations of the RC is discussed.     

Effect of high intracellular calcium ion concentration on the transmembrane current induced by iontophoretic injection of cAMP inHelix pomatia neurons

The effect of increasing the intracellular calcium ion concentration by various methods (iontophoretic injection into the cytoplasm, generation of a burst of action potentials, addition of uncouplers of oxidative phosphorylation to the external solution, causing release of calcium from mitochondria) on the inward current induced by injection of cAMP into the neuron (the cAMP current) was investigated on the neuron membrane ofHelix pomatia under voltage clamp conditions. In all cases an increase in the intracellular calcium ion concentration was found to lead to an increase in amplitude, and in many cases duration, of the cAMP current. It is suggested that membrane structures responsible for appearance of the cAMP current have two phosphorylation centers: cAMP-dependent and calcium-calmodulin-dependent. The possible role of this process in signal integration at the intraneuronal level is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 17, No. 1, pp. 78–84, January–February, 1985.     

Electron cytochemical study of carbogydrate components of surface membrane in cultured glial cells of the snailHelix pomatia

Using a variety of colloidal gold-labelled lectins, the structure and topography of carbohydrate determinants of the surface membrane in different types of cultured glial cells of the snailHelix pomatia have been electron cytochemically investigated. Analysis of lectin binding having different sugar specificities have shown heterogeneity of carbohydrate pools between glial and nerve cells and among different types of glial cells. It was found that satellite glial cells displaying ultrastructural traits of intensive metabolism (type II cells) selectively bindGNA, which is specific for terminal -D-mannose residues, and do not interact (Con A) or slightly interact (LCA) with other mannose-specific lectins.GNA determinants remain during the whole period of cell growth and are absent in satellite type-I glial cells, fibrous glial cells, microglia, and neurons.LTA, PVA, andLABA do not bind to any glial cells.WGA determinants, which are abundant on the neurons, are completely absent onGNA-binding glial cells and single on other types of glial cells. The density ofPNA determinants on microglial cells is the highest, as compared with other types of glial cells or neurons. It is concluded that some lectin determinants (forRCA-1, PNA, LPA) are present on all types of glial cells, while another determinant (GNA) is specific for a certain type of glial cells only and can serve as a marker of these cells. The role of specific carbohydrate determinants for neuron-glia interaction in mature brain is discussed.Neirofiziologiya/Neurophysiology, Vol. 26, No. 3, pp. 177–189, May–June, 1994.     

Organization of fusicoccin receptor in higher plant plasma membrane: relationship between affinity and molecular mass

Higher plant plasma membranes carry receptors of different affinity for the phytotoxin fusicoccin. Reception of fusicoccin involves proteins belonging to the highly conserved 14-3-3 family, but the complete structure of the fusicoccin receptor (FCR) is unknown. Using radiation inactivation analysis, we estimated the molecular masses of low-affinity and high-affinity FCR at 63 +/- 7 and 130 +/- 15 kD, respectively. The dose dependences of receptor inactivation indicate that microsomal specimens contain "silent" FCRs of 420 +/- 90 kD in amounts commensurate with that of the active FCRs. Both low- and high-affinity FCRs are inactivated by hydrolytic enzymes from the outer surface of the plasma membrane, and impairment of protoplast integrity causes an irreversible transition of the low-affinity binding site into the high-affinity one. A scheme is proposed for the organization of different types of FCR in the plasma membrane, implying that the membrane affinity for fusicoccin reflects the interaction between proteins in the FCR complex.     

Effect of intracellular injection of cyclic amp on electrical characteristics of identified neurons in Helix pomatia

The effect of intracellular iontophoretic injection of cyclic AMP on electrical activity of neurons RPa1, RPa3, LPa2, LPa3, and LPl1 in the corresponding ganglia ofHelix pomatia was investigated. Injection of cyclic AMP into neuron LPl1 was found to cause the appearance of rhythmic activity (if the neuron was originally "silent"), an increase in the frequency of spike generation (if the neuron had rhythmic activity), and a decrease in amplitude of waves of membrane potential, in the duration of the interval between bursts, and in the number of action potentials in the burst (if the neuron demonstrated bursting activity). In the remaining "silent" neurons injection of cyclic AMP led to membrane depolarization. Injection of cyclic AMP into neurons whose membrane potential was clamped at the resting potential level evoked the development of an inward transmembrane current (cyclic AMP current), the rate of rise and duration of which increased proportionally to the size and duration of the injection. Theophylline in a concentration of 1 mM led to an increase in the amplitude and duration of the cyclic AMP current by about 50%. It is concluded that a change in the cyclic AMP concentration within the nerve cell may modify the ionic permeability of its membrane and, correspondingly, its electrical activity.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 12, No. 5, pp. 517–525, September–October, 1980.     

Kinetic dimensions of cells and crypts in irradiated intestinal epithelium of mice]

The average value of axial cryptal section area and cell section area on it were studied during 8 days after total X-ray irradiation of male mice (400 rad). A small reducing of cryptal area (20%) during destructive period (1-2 days) is followed by a big overshoot (60%) during regenerative time (3-7 days). The cryptal sizes in regenerative period deviate from a steady state more than during destructive time. There are two high waves of abnormal growth of cell sizes above the steady level: the first one during destructive time and the second one during regeneration. This level seems to be near to minimal sizes of cryptal proliferative cells which are necessary for proliferation. It means that normal intestinal epithelium is a very economical and stabilized system. It is possible to evaluate quantitatively the associated with proliferation flow of substance per crypt cell for normal and irradiated intestine by means of index Iv where I is mitotical index and v - the cell volume. Cell hypertrophy at the time of regeneration on the 4th-7th days and later after irradiation (130-160%), was revealed. The crypt cell hypertrophy is the factor of destabilization of irradiated intestinal epithelium.