M. N. Repkova, O. Yu. Mazurkov, E. I. Filippova, M. A. Procenko, N. A. Mazurkova, B. P. Chelobanov, A. S. Levina, V. F. Zarytova
{"title":"Oligoribonucleotide-Containing Nanocomplexes Based on Aminopropylsilanol Nanoparticles as Effective Inhibitors of Influenza A Virus Replication","authors":"M. N. Repkova, O. Yu. Mazurkov, E. I. Filippova, M. A. Procenko, N. A. Mazurkova, B. P. Chelobanov, A. S. Levina, V. F. Zarytova","doi":"10.3103/s0096392524600431","DOIUrl":"https://doi.org/10.3103/s0096392524600431","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>Titanium dioxide or aminopropylsilanol nanoparticles were shown to be effective vehicles for delivering oligodeoxyribonucleotides and deoxyribozymes to cells to affect target nucleic acids. In this paper, the proposed principle of the delivery has been implemented in relation to oligoribonucleotides (ORN), components of short interfering RNAs (siRNAs). It has been shown that the obtained ORN-containing nanocomplexes (Si~NH<sub>2</sub>·ORN) based on aminopropylsilanol nanoparticles penetrate eukaryotic cells. These nanocomplexes have been investigated as agents for suppressing the replication of influenza A virus (IAV) in the cellular system. It has been shown that the ORN strands targeted to (+)RNA and (–)RNA of the IAV 5th segment reduces the titer of the virus by 99.7% and 98.4%, respectively. Thus, oligoribonucleotides in the Si~NH<sub>2</sub>·ORN nanocomplexes effectively inhibit the replication of the influenza A virus.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"19 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140302747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
J. A. Amao, P. F. Omojasola, A. A. Ayandele, A. G. Adewoyin
{"title":"Enzyme and Biosurfactant Production by Exopolysaccharide Producing Bacteria Isolated from Cassava Peel Heaps","authors":"J. A. Amao, P. F. Omojasola, A. A. Ayandele, A. G. Adewoyin","doi":"10.3103/s0096392523600254","DOIUrl":"https://doi.org/10.3103/s0096392523600254","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>A major one among bacteria used in the commercial production of enzymes is <i>Bacillus</i> sp.; others include <i>Escherichia</i> sp., <i>Pseudomonas, Proteus, Serratia,</i> and <i>Rhizobium,</i> which also yield an appreciable quantity of enzymes. Biosurfactants naturally play a vital role in the teeming motility of microbes and contribute to cellular physiological procedures of signalling and, differentiation, and biofilm formation. The sourcing and selection of microbes from natural sources have endlessly been shown to be an effective way of identifying isolates of industrial value. The current study aimed to determine the ability of exopolysaccharide-producing bacteria isolated from cassava peel heap to produce some extracellular enzymes and biosurfactants. Thirteen bacteria earlier isolated from cassava peel heaps samples and found to be exopolysaccharide producers were used in this study. The highest xylanase activity was recorded at 40°C by <i>B. amyloliquefaciens</i> (J47). Titratable acid content was highest in peel fermented with isolate <i>Lactobacillus plantarum</i> (J18)<i>.</i> In contrast, the pH of fermented peel fell below pH 7, with the lowest being the peel fermented by <i>Pectobacterium carotovorum</i> (J36)<i>.</i> Three <i>Bacillus</i> spp. (<i>Bacillus</i> sp. J1, <i>Bacillus</i> <i>subtilis</i> J2, and <i>B. amyloliquefaciens</i> J47) were able to produce all the three enzymes (xylanase, cellulase, and β-glucosidase) assayed for. Bacterial isolates from cassava peel heap can be helpful in many industrial processes with their ability to produce substances of industrial value.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"19 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140302748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Rheological Behavior of Polysaccharide Hydrogels of Alginate Reinforced by a Small Amount of Halloysite Nanotubes for Extrusion 3D Printing","authors":"V. S. Molchanov, S. A. Glukhova, O. E. Philippova","doi":"10.3103/s0096392523700268","DOIUrl":"https://doi.org/10.3103/s0096392523700268","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>The rheological properties of hydrogels of a natural polysaccharide sodium alginate and small amount of clay nanotubes of halloysite were investigated. Changes of rheological properties during the transition from a semidiluted polymer solution to a hydrogel upon cross-linking by calcium ions were shown. In the gel state, the samples have a yield stress, and their viscosity decreases with the shear rate, but the properties are quickly recovered after the load removal. It was discovered that the addition of up to 0.3 vol % nanotubes of natural clay halloysite leads to an increase by several times of a storage modulus and a yield stress of the hydrogels. At the same time, the practically important properties of shear thinning and the rapid recovery of properties after the load removing make the nanocomposite hydrogels of alginate and halloysite nanotubes promising for use as ink for extrusion 3D printing.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"122 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Patterns of a Disulfide Bond Formation in Toxins of Spiders from the Ctenidae Family: A Comparison with Predictions of the AlphaFold 2.0 Neural Network","authors":"P. A. Mironov, Z. O. Shenkarev","doi":"10.3103/s0096392523700141","DOIUrl":"https://doi.org/10.3103/s0096392523700141","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>Venoms of wandering or running spiders from the family Ctenidae are multicomponent and include >500 identified peptides and proteins called ctenitoxins. The main components of the venom are cysteine-rich peptides containing an inhibitor cystine knot (ICK) motif. The pharmacological diversity of ctenitoxins makes it possible to consider some of them as prototypes for the development of new drugs to treat chronic pain, Huntington’s disease, erectile dysfunction, and glaucoma. Based on the localization of cysteine residues in the amino acid sequence, ctenitoxins are divided into 14 groups containing 6–14 Cys residues. To date, the spatial structure of only one ctenitoxin, ω-CNTX-Pn4a (Pha1β or Tx3-6) from the Brazilian wandering spider <i>Phoneutria nigriventer</i>, has been determined. Another ten structural groups of ctenitoxins are homologous to the known spatial structures of toxins from other spider families or other proteins; finally, three more ctenitoxin groups do not have any known structural homologues. In this study, we proposed possible patterns for the disulfide bond formation in all ctenitoxin groups. A comparison of the obtained schemes with the predictions of the AlphaFold 2.0 algorithm shows that this neural network does not always correctly predict the structure of cysteine-rich peptides, especially in the case of modeling of mature peptides without leader sequences.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"35 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Structural Heterogeneity and Diversity of Bacillus subtilis 168 Biofilms under Different Conditions","authors":"T. Osire, Y. Wang, O. Burtseva, O. S. Sokolova","doi":"10.3103/s0096392523700190","DOIUrl":"https://doi.org/10.3103/s0096392523700190","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>Bacteria usually dwell in microbial communities of biofilms surrounded by a self-secreted extracellular matrix. This work assessed effects of different media and temperature on the development of <i>Bacillus subtilis</i> 168 biofilms. We applied Scanning Electron Microscopy to analyse structural differences of the pellicle biofilms grown on LB, NB, and DMS media. Significant differences were observed in biofilm morphology, and unit cell length, highlighting the significance of intricate aspects such as nutrients in bacterial/ biofilm growth. Our findings reveal the adaptation tendency of bacterial through spatial modification of its biofilm structure in response to surrounding environmental conditions such as nutrients, temperature among others, perhaps explaining variations in biofilm morphologies observed. The results present an information on biofilm diversity which could be essential for biofilm applications.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"283 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Cryoconveyor Protocols in Correlative Light and Electron Microscopy: From Multilevel Imaging to Modeling the Biophysical Effects and “Cryotheranostics”","authors":"O. V. Gradov","doi":"10.3103/s0096392523700244","DOIUrl":"https://doi.org/10.3103/s0096392523700244","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>This paper is a technical and methodological note aimed to introduce into the practice of biological research methods a cryomicroscopy in a conveyor mode from small magnifications to the limits of magnification/resolution of scanning electron cryomicroscopy (CryoSEM). The protocol described can be applied to the samples of a low sample preparation complexity without ultratomy or processing typical of transmission electron microscopy. According to this protocol, samples are analyzed in a single microcuvette (chip) indexed by laboratory information management system and sequentially transferred from the nondestructive low-resolution optical microscopy instruments, such as lensless cryo-microscopes, to the CryoSEM/CryoESEM level (in programmable environments and atmospheres). Methods that were introduced and tested include correlative lensless cryomicroscopy and CryoSEM (including those with the sequential transition to microanalysis on wavelength-dispersive X-ray spectrometer on the Rowland circle) as well as microscopy and microinterferometry methods in the ranges from infrared to far-ultraviolet. Among the advantages of the cryoconveyor analysis protocols are sample preservation in a single portable cuvette-chip along with a possibility to establish spatial colocalization between data of optical and electron microscopy using pattern recognition software (all the way to indexing in the laboratory information system) in conducting a full range of microscopic examination. An opportunity is additionally provided for a comprehensive nondestructive sample analysis in a sequential study of microscopic systems with a possibility of variation at the subsequent stages of high-resolution microscopy, depending on the results obtained at the preceding stages of microscopy (at lower resolution).</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"28 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097926","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. V. Moiseenko, A. M. Egorov, K. V. Shaitan, O. S. Sokolova
{"title":"Cryo-Electron Microscopy at the Biological Faculty of Moscow State University","authors":"A. V. Moiseenko, A. M. Egorov, K. V. Shaitan, O. S. Sokolova","doi":"10.3103/s0096392523700232","DOIUrl":"https://doi.org/10.3103/s0096392523700232","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>The paper reports an example of a successful upgrade of the JEOL JEM-2100 analytical transmission electron microscope to a low-resolution cryo-electron microscope, which can be used to optimize sample preparation and to assess preparation quality. As a result of the instrument upgrade, it is possible to obtain subnanometer resolution of protein molecule reconstructions (within 8 Å). The role of graphene and amorphous carbon substrates in preventing the effect of preferential orientation of protein particles in a frozen sample is discussed.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"16 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Structural Study of the Candida auris Ribosome","authors":"A. A. Atamas, A. I. Guskov, A. V. Rogachev","doi":"10.3103/s0096392523700220","DOIUrl":"https://doi.org/10.3103/s0096392523700220","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p><i>Candida auris</i> is a pathogenic fungus that causes infections in people with weakened immune systems. It is resistant to antimicrobial drugs, which complicates treatment. <i>C. auris</i> poses a serious threat to public health since it has high resistance and contagiousness. The ribosome plays an important role in the survival and development of this infection, and the search for inhibitors of the <i>C. auris</i> ribosome is of great importance. The authors used cryoelectron microscopy and single particle analysis to obtain the three-dimensional structure of the <i>C. auris</i> ribosome. Herein is described the architecture of the ribosome subunits and their interactions, providing valuable information for the development of novel antifungals against <i>C. auris</i>.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"44 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097707","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
I. V. Demianova, E. A. Akoulina, I. I. Zharkova, V. V. Voinova, D. V. Chesnokova, A. M. Hossain, T. K. Makhina, G. A. Bonartseva, V. I. Kulikouskaya, V. V. Nikalaichuk, Yu. R. Mukhortova, A. S. Pryadko, M. A. Surmeneva, R. A. Surmenev, K. V. Shaitan, A. P. Bonartsev
{"title":"Growth of Mesenchymal Stem Cells on Oriented Microstructured Films and Electrospun Scaffolds","authors":"I. V. Demianova, E. A. Akoulina, I. I. Zharkova, V. V. Voinova, D. V. Chesnokova, A. M. Hossain, T. K. Makhina, G. A. Bonartseva, V. I. Kulikouskaya, V. V. Nikalaichuk, Yu. R. Mukhortova, A. S. Pryadko, M. A. Surmeneva, R. A. Surmenev, K. V. Shaitan, A. P. Bonartsev","doi":"10.3103/s0096392523700189","DOIUrl":"https://doi.org/10.3103/s0096392523700189","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>The study involved the fabrication of films with different roughness and scaffolds made of poly-3-hydroxybutyrate using various methods. Chaotic and oriented scaffolds with varying fiber thickness were obtained through the electrospinning method, depending on the polymer concentration and electrospinning parameters. Films with different surface roughness were obtained using spin coating and self-assembly methods. It was demonstrated that the varying microstructure of the surface does not affect the growth of mesenchymal stem cells over the course of 1 week; however, it does influence the morphology of the adhered cells.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"283 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. A. Glukhova, G. Lu, K. V. Shaitan, D. V. Bagrov, G. S. Glukhov
{"title":"Single-Molecule Imaging of Ion Channels Isolated in Detergent and Styrene-Maleic Acid Copolymer","authors":"A. A. Glukhova, G. Lu, K. V. Shaitan, D. V. Bagrov, G. S. Glukhov","doi":"10.3103/s0096392523700177","DOIUrl":"https://doi.org/10.3103/s0096392523700177","url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>In this work we purified <i>Shaker</i> ion channel using two alternative techniques – the detergent-based (CHAPS) and styrene-maleic acid copolymer lipid particles (XIRAN-based). Using XIRAN-based technique, we can obtain higher yield of purified protein. We used atomic force microscopy and transmission electron microscopy methods to visualize the purified single molecules. Atomic force microscopy allows measuring the diameter of the single molecules but does not reveal any high-resolution details. The sizes of individual <i>Shaker</i> molecules isolated by the two purification methods were close to each other.</p>","PeriodicalId":19004,"journal":{"name":"Moscow University Biological Sciences Bulletin","volume":"37 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140097745","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}