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Biomedical subjects

V Z Pashchenko

Publications and source records attributed to V Z Pashchenko.

At least 19 recordsLinked to original sources
PubMed2005

Role of viscosity and permeability of the erythrocyte plasma membrane in changes in oxygen-binding properties of hemoglobin during diabetes mellitus.

Changes in viscosity and permeability of the plasma membrane and conformation of erythrocyte hemoglobin hematoporphyrin were found in patients with diabetes mellitus. The decrease in oxygen binding and increase in deoxyhemoglobin concentration during diabetes mellitus were accompanied by changes in viscosity and permeability of the membrane for Na+, H+, Ca2+, and K+. Our results suggest that oxygen-binding properties of hemoglobin depend on viscosity and permeability of the erythrocyte plasma membrane.

Calcium↗
PubMed2000

Investigation of the electron transfer reactions and redox characteristics of photoactive bacteriochlorophyll in Rhodobacter sphaeroides reaction centers modified by D2O and cryoprotectants.

The effects of D2O, glycerol and dimethyl sulfoxide (DMSO) on redox potential Em of bacteriochlorophyll of a special P2 or [P(M)P(L)] pair, the rate of energy migration from bacteriopheophytin H(M) to [P(M)P(L)], electron transfer from [P(M)P(L)] to bacteriopheophytin H(L) and then to quinone Q(A) in reaction centers (RC) of Rhodobacter sphaeroides were studied. The H2O --> D2O substitution did not change Em of the special pair, whereas addition of 70% glycerol or 35% DMSO (v/v) increased the values of Em by 30 and 45 mV, respectively. Rate constants of energy migration km(H(M)* (km)--> P2), charge separation ke([P(M)P(L)] *H(L) (ke)--> [P(M)P(L)] +H(L)-), electron transfer to quinone kQ did not change after the glycerol addition, whereas isotopic substitution and addition of DMSO caused a 2-3-fold increase in km, ke, and kQ values. Theoretical analysis of the redox center potential dependence on dielectric permeability epsilon, swelling of the protein globule in a solvent, and on changes in the charge distribution (charge shifts) in the protein interior near the redox center was carried out. It has been shown that the H2O replacement with DMSO can result in the Em increase by tens of mV. No correlation was found between the Em values and the rate of charge separation upon isotopic substitution and addition of cryoprotectants. The effect of epsilon of the medium on the rate of electron transport due to changes of energy of intermolecular interaction between the donor and acceptor molecules was estimated.

Bacteriochlorophylls↗
PubMed1992

[The mechanisms of the porphyrin conformation of normal blood hemoglobin and in pathology].

The spectra of resonance Raman scattering of blood in norm and under pathology (myocardial infarction and sepsis), as well after artificial hemotransfusion or UV photomodification have been studied. It has been shown that under heart pathology the structure of hemoglobin porphyrin macrocycle of erythrocytes changes, the size of porphyrin "nucleus" increases. The opposite conditions are observed at blood sepsis. It has been found that the traditional methods in tissue restoration, hemotransfusion and UV photomodification of blood don't result in complete restoration of hemoporphyrin molecule.

Blood↗
PubMed1989

[Molecular mechanisms of the action of local anesthetics].

Raman spectroscopy revealed a suppression of the polyene chain of C40-carotenoids in membrane of the frog nerve during local action of an anesthetic agent in resting and excitation. The phosphatidylcholine binding decreased during rhythmic excitation and local anesthetic action. A mechanism of potential-dependent changes of the carotenoid conformation during local anesthetic action, was discussed.

Action Potentials↗
PubMedDate not supplied

[Relation between structural-dynamic organization of reaction centers in Rhodobacter sphaeroides and picosecond steps of photosynthesis].

The effect of deuteration, and the addition of glycerol and dimethylsulfoxide on the redox midpoint potential Em of bacteriochlorophyll of the special pair ¿PMPL¿, the rate of energy migration from bacteriopheophytin HM to ¿PMPL¿, and electron transfer from ¿PMPL¿ to HL and from HL to quinone QA in reaction centers of Rhodobacter sphaeroides was studied. It was shown that H2O-->D2O substitution did not change Em of the special pair, while the addition of 70% glycerol and 35% dimethylsulfoxide (v/v) increased the Em value by 30 and 45 mV, correspondingly. The rate constants of energy migration [formula: see text], charge separation [formula: see text], electron transfer to QA kQ remained unchanged upon the addition of glycerol. The isotopic substitution of water and addition of dimethylsulfoxide led to a 2-3-fold increase in km, ke and kQ values. The dependence of the potential of redox center on the dielectric constant epsilon was analyzed. It was shown that replacement of H2O by dimethylsulfoxide can increase Em by tens of millivolt. There was no correlation between changes in Em and the values of km, ke and kQ upon deuteration and addition of cryoprotectors. It was concluded that the processes of energy migration, charge separation, and electron transfer to the quinone acceptor are preceded by the solvation of states H*M, ¿P+MP-L¿* and [formula: see text].

Light-Harvesting Protein Complexes↗
PubMedDate not supplied

[Isolation and characterization of photochemical properties of the photosynthetic reaction centers from Rhodopseudomonas shperoides, strain 1760-1].

Photosynthetic reaction centres were isolated from the cells of Rhodopseudomonas spheroides, strain 1760-1, using sodium dodecyl sulphate. The preparations purified by precipitation with ammonium sulphate showed absorbance ratios of A280 : A800=2.1. and A765 : A800 : A870=1 : 2 : 1; about 75% of the bacteriochlorophyll absorbing at 870 nm (P870) were photochemically active. Both absolute and difference "light minus dark" absorption spectra were obtained for the reaction centre suspensions and vacuum-dried films at room and low temperatures. Shift to the longer wavelength of the 870 nm absorption band resulting from temperature lowering suggests the existence of temperature-determined conformations of the bacteriochlorophyll-protein complex of the reaction centres. Characteristic time of an electron transfer from the photoexcited P870 to the primary intermediate of photochemical process as evaluated from the data of pulsed laser fluorometry of the reaction centres was found to be (21--15)+/-8 picoseconds. The oxidized P870 dark reduction kinetics dependence on the actinic light intensity gives evidence for the functioning of heterogeneous pool of the secondary electron acceptors in the reaction centre preparations. Filling in of this pool with electrons is decreased under temperature lowering or vacuum drying and its electron capacity is limited under isooctane treatment resulting in ubiquinon extraction. The ability of the reaction centre preparations to catalyze the photochemical oxidation of iminoxyl aromatic radical was demonstrated.

Bacteriochlorophylls↗
PubMedDate not supplied

[Effects of relaxation processes on the temperature dependence of oxidation rate of photooxidized bacteriochlorophyll on the primary quinone in reaction centers of Rhodobacter sphaeroides].

The temperature dependence of the time of dark recombination of charges between photooxidized bacteriochlorophyll and reduced primary quinone acceptor (tau e) in Rhodobacter sphaeroides photosynthetic reaction centers was studied in the temperature range 140-320 K. It was found that the function tau e = tau e(T) is nonmonotonous: in the temperature range from 140 to 290 K, tau e is increased from 40 to 100 ms; however, under further heating to 320 K, tau e decreased to 80 ms. The replacement of H2O by D2O in these preparations caused an acceleration of the recombination process in the range of physiological temperatures, but the nonmonotonous character of the function tau e(T) remained. The theoretical interpretation of the results was made in the framework of the theory of electron-phonon interactions with allowance for the relaxation processes.

Algorithms↗
PubMedDate not supplied

[Possible effect of structural phase transition in the reactive center of Rhodobacter sphaeroides on the rate of dark adaptation of photooxidized bacteriochlorophyll from primary quinone].

The dependence of the rate of dark recombination between the photooxidized primary donor--dimer bacteriochlorophyll molecule (P) and reduced primary quinone acceptor (QA), P+QA(-)-->PQA was studied in photosynthetic reaction centers (RC) from Rhodobacter sphaeroides in the temperature range of 100-320 K. Control RC preparations, RC species with the removed H-subunit as well as RC samples with the hydrogen bonds network modified by isotopic D2O-H2O substitution were investigated. An anomalous temperature dependence of the recombination time (tau rec) of dark reaction P+QA(-)-->PQA was found for all RC samples. It was found that upon heating from 120 to 290 K tau rec increased 2.5 fold. However, upon further heating to 320 K, tau rec decreased again. The temperature dependences of the P+QA(-)-->PQA recombination time were compared with those of the thermodepolarization current of RC preparations in the same temperature range. The temperature curve of the thermodepolarization current was also nonmonotonous. The theoretical interpretation of the temperature dependence of tau rec as well as of the thermodepolarization current was made in the framework of the theory of structural phase transitions within the hydrogen bond network in the water-protein surrounding of the redox centers participating in the electron transfer reactions.

Bacteriochlorophylls↗
PubMedDate not supplied

[A network of hydrogen bonds in the reaction centers of Rhodobacter sphaeroides serves as a regulatory factor of the temperature dependence of the recombination rate constant of photooxidized bacteriochlorophyll and primary quinone acceptors].

The dark recombination rate constant for the photooxidized bacteriochlorophyll (P) and reduced primary quinone acceptor (QA) in the photosynthetic reaction centers (RC) from purple bacterium Rhodobacter sphaeroides depends nonmonotonically on temperature. The time of this reaction is approximately 100 ms at 270-300 K and decreases as the temperature both increases and decreases beyond this temperature range. It is known that the dome-shaped dependence of the thermodynamic stability on temperature is an intrinsic feature of many proteins in solution. The experimental results on the nonmonotonous temperature dependence of P+ and QA- recombination rate constant are discussed in terms of general thermodynamic approaches. The dynamic properties of the network of hydrogen bonds that are involved in the relaxation processes accompanying the electron transport are considered as a regulatory factor of the efficiency of electron transfer.

Bacteriochlorophylls↗
PubMedDate not supplied

[The application of PS II model for the analysis of fluorescence yield transients induced by actinic single turnover flash in the time range from 100 ns to 10 s].

Changes in flash-induced fluorescence yield in preparations of thermophilic Chlorella pyrenoidosa Chick cells (native and in the presence of DCMU) were investigated in the time range from 100 ns to 10 s using a new measuring system. The results were analyzed by mathematical modeling of processes in photosystem II. It was shown that the detailed description of recombination (including nonradiative) processes in photosystem II is important to simulate the fluorescence yield transients induced by an actinic single turnover flash. The model photosystem II parameters were modified to describe the light-induced effects in the presence of DCMU. By comparing the theoretical fluorescence curves with experimental ones, we obtained the values of relative fluorescence yield and the FM/F0 ratio, which is typical for experimental data. As a result of simulation, the values of the model parameters (rate constants of electron transfers at the donor and acceptor sites of photosystem II, pH in stroma, initial redox state of the plastoquinone pool, the rate of plastoquinol oxidation, and the rate constants of nonradiative recombination processes) were determined.

Chlorella↗