Immunogenic Properties of the DNA Construct Encoding the Receptor-Binding Domain of the SARS-CoV-2 Spike Protein

Molecular Biology - The development of preventive vaccines became the first order task in the COVID-19 pandemic caused by SARS-CoV-2. This paper reports the construction of the pVAX-RBD plasmid...     

Effect of Furostanol Glycosides from Dioscorea deltoidea on Redox State of Alfalfa Cells In Vitro

Russian Journal of Plant Physiology - The effect of exogenous furostanol glycosides (FG) on the activity of redox enzymes was investigated in suspension cell culture of alfalfa (Medicago sativa...     

Adaptogenic action of the complex of phenylpropanoids on Dioscorea deltoidea cell culture under abiotic stress

Biological activity of the extract from golden root (Rhodiola rosea L.) roots, containing the complex of phenylpropanoids (CPP), was studied on the cell culture of yam (Dioscorea deltoidea Wall) under normal conditions and abiotic stress. The high radical-binding capacity of CPP relative to anion- and hydroxyl-radicals was observed. Having a high level of antiradical protection, CPP at a high concentration(100 μM) exerted prooxidant effect, causing a decrease in D. deltoidea cell viability and a decrease in the activities of antioxidant enzymes: superoxide dismutase, guaiacol-dependent peroxidase, and catalase, with the exception of ascorbate peroxidase. At treatment with 100 μM CPP, oxidase (prooxidant) activity of peroxidase increased by three times. The low CPP concentration (2 μM) did not induce substantial changes in the activities of tested enzymes and also a substantial increase in the oxidase activity of peroxidase. Under conditions of oxidative stress induced by paraquat and high temperature, CPP manifested adaptogenic action, increasing cell viability; however, under hyperosmotic stress, it was not efficient. CPP was most efficient at a low concentration after cell pre-incubation with it for 5 days. In this case, the amount of primary and secondary POL products increased. Shortening pre-cultivation with CPP reduced its defensive effect.     

N-Methyl-D-Aspartate Receptor Function Observed by Rate of Ligand Dialysis From Proteoliposome Solution

Abstract

This study reports rate-of-dialysis of an iodinated N-methyl-D-aspartate antagonist drug, [125-1] MK-801, from solutions of lipid vesicles and from proteoliposomes containing purified membrane proteins. A 170 kd protein precipitated from proteoliposomes cross reacts with monoclonal antibodies against cloned NMDA-NR2(A) and NR2(B) subunits. Drug binding in proteoliposomes includes contributions from lipid and from protein, in addition to lipid. A significant change in drug binding was observed in proteoliposomes in response to 10 uM agonist, NMDA. Rate-of-dialysis from agonist-stimulated proteoliposomes was sensitive to perturbation by decreased aqueous ligand concentration in a manner consistent with a lipid-mediated receptor/antagonist equilibrium.     

Sensitivity of antioxidant status of plant cells to furostanol glycosides

The present paper reports that in vitro plant objects (test tube plants and cell cultures), when subjected to furostanol glycosides (FG), underwent nonspecific reactions related to antioxidant status—decrease in peroxidation of lipids (POL) and increase in guaiacol-dependent peroxidase activity. The level of superoxide increased as early as after 5 min from contact with yam (Dioscorea deltoidea Wall) cells with FG. In this case, changes in POL processes and in activities of peroxidase and aldehyde-disposing emzymes were also observed. Upon a short-term cell exposure to FG, the levels of the primary POL products (conjugated dienes) increased, and that of the secondary POL products decreased compared to the control. These events were preceded by a rise in SOD activity and in an antioxidant activity of peroxidase along with a concurrent decrease in its oxidase (prooxidant) activity. The elevated activities of aldehyde-disposing enzymes aldehyde dehydrogenase and aldehyde reductase favored the reduction in the content of the secondary products of POL. Upon a long contact of FG with cells, the effect of FG was seen only at the initial and final phases of the culture growth cycle. Namely, FG diminished the POL level at the exponential growth phase and at the end of the cell degradation phase but had no effect at the stationary phase and the onset of the degradation phase. Therefore, the treatment with FG retarded the cell culture degradation and made the fall in cell viability not so dramatic by the end of the growth cycle. Actually, by the end of the degradation phase, the viability diminished down to 40% in the control but remained at 70% in the FG-treated counterpart.     

Matrix metalloproteinases as target genes for gene regulatory networks driving molecular and cellular pathways related to a multistep pathogenesis of cerebrovascular disease

The present study investigated a joint contribution of matrix metalloproteinases (MMPs) genes to ischemic stroke (IS) development and analyzed interactions between MMP genes and genome-wide associated loci for IS. A total of 1288 unrelated Russians (600 IS patients and 688 healthy individuals) from Central Russia were recruited for the study. Genotyping of seven single nucleotide polymorphisms (SNPs) of MMP genes (rs1799750, rs243865, rs3025058, rs11225395, rs17576, rs486055, and rs2276109) and eight genome-wide associated loci for IS were done using Taq-Man–based assays and MALDI-TOF mass spectrometry iPLEX platform, respectively. Allele − 799T at rs11225395 of the MMP8 gene was significantly associated with a decreased risk of IS after adjustment for sex and age (OR = 0.82; 95%CI, 0.70-0.96; P = 0.016). The model-based multifactor dimensionality reduction method has revealed 21 two-order, 124 three-order, and 474 four-order gene-gene (G×G) interactions models meaningfully (P_perm < 0.05) associated with the IS risk. The bioinformatic analysis enabled establishing the studied MMP gene polymorphisms possess a clear regulatory potential and may be targeted by gene regulatory networks driving molecular and cellular pathways related to the pathogenesis of IS. In conclusion, the present study was the first to identify an association between polymorphism rs11225395 of the MMP8 gene and IS risk. The study findings also indicate that MMPs deserve special attention as a potential class of genes influencing the multistep mechanisms of cerebrovascular disease including atherosclerosis in cerebral arteries, acute cerebral artery occlusion as well as the ischemic injury of the brain and its recovery.     

Plant growth-promoting Pseudomonas bearing catabolic plasmids: Naphthalene degradation and effect on plants

Two IncP-9 naphthalene degradative plasmids pOV17 and pBS216 were transferred into plant growth-promoting Pseudomonas which were represented by species P. aureofaciens, P. chlororaphis, P. fluorescens, and P. putida. The strains with the same plasmid differed significantly by their growth parameters, stability of the plasmid and plant protective effect from naphthalene action. Strains P. putida 53a(pOV17) and P. chlororaphis PCL1391(pOV17) demonstrated higher population number in the rhizosphere. Moreover, they protected the mustard plants from naphthalene toxic influence more effectively than the wild type strain P. aureofaciens OV17(pOV17). The activity of catechol-2,3-dioxygenase in the strains with the plasmid pOV17 was higher than that in strains with the plasmid pBS216. The strain P. putida 53a(pOV17) with high catechol-2,3-dioxygenase activity has been demonstrated to have the best protective effect. The strain P. putida 53a(pBS216) without catechol dioxygenases activities did not have protective effect but suppressed the plant germination.     

Detection of nanodiamonds in biological samples by EPR spectrometry

In model experiments in vitro, the applicability of the EPR spectrometry method for the detection of modified nanodiamonds (MNDs) in blood and homogenates of mouse organs has been established. A characteristic signal (g = 2.003, ΔH ≈ 10 G) is observed in the samples of biomaterials containing MNDs, the intensity of which increases linearly with the concentration of nanoparticles in the range of 1.6–200 μg MNDs per 1 mL of the sample. The EPR method in biomaterials reveals the presence of intrinsic paramagnetic centers, signals from which are superimposed on the signal from the MNDs. However, the intensity of these signals is small, which makes it possible to register the MNDs using EPR spectrometry with the necessary accuracy. The data obtained open up the prospects of using the EPR method for studies of the interorgan distribution, accumulation, and elimination of MNDs during their intravenous injection into experimental animals.