1,194 results match your criteria: "* Institute of Protein Research[Affiliation]"

Polyribosomes, the groups of ribosomes simultaneously translating a single mRNA molecule, are very common in both, prokaryotic and eukaryotic cells. Even in early EM studies, polyribosomes have been shown to possess various spatial conformations, including a ring-shaped configuration which was considered to be functionally important. However, a recent in situ cryo-ET analysis of predominant regular inter-ribosome contacts did not confirm the abundance of ring-shaped polyribosomes in a cell cytoplasm.

View Article and Find Full Text PDF

Membrane trafficking in interphase animal cells is accomplished mostly along the microtubules. Microtubules are often organized radially by the microtubule-organizing center to coordinate intracellular transport. Along with the centrosome, the Golgi often serves as a microtubule-organizing center, capable of nucleating and retaining microtubules.

View Article and Find Full Text PDF

Structural and Functional Characterization of β-lytic Protease from VKM B-2533.

Int J Mol Sci

December 2022

Laboratory of Microbial Cell Surface Biochemistry, G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, FRC PSCBR, Russian Academy of Sciences, 5 Prosp. Nauki, 142290 Pushchino, Russia.

Article Synopsis
  • The crystal structure of VKM B-2533 β-lytic protease (Blp) was successfully determined, identifying its similarity to the M23 protease family.
  • Comparisons between Blp and the LasA structural homologue showed differences in the amino acids of their active site grooves, despite no variations in optimal reaction conditions for their bacteriolytic activities.
  • Blp demonstrates a wider range of effectiveness against various target cells, suggesting that the geometry and charge of amino acids in the active site groove influence its ability to break down different types of peptidoglycan.
View Article and Find Full Text PDF

Interleukin-17 (IL-17) is a cytokine produced by the Th17 cells. It is involved in chronic inflammation in patients with autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, and psoriasis. The antibodies targeting IL-17 and/or IL-17R are therapy tools for these diseases.

View Article and Find Full Text PDF

Many proteins form amyloid fibrils only under conditions when the probability of transition from a native (structured, densely packed) to an intermediate (labile, destabilized) state is increased. It implies the assumption that some structural intermediates are more convenient for amyloid formation than the others. Hence, if a mutation affects the protein folding pathway, one should expect that this mutation could affect the rate of amyloid formation as well.

View Article and Find Full Text PDF

The repetitive copying of template nucleotides due to transcriptional slippage has not been reported for RNA-directed RNA polymerases of positive-strand RNA phages. We unexpectedly observed that, with GTP as the only substrate, Qβ replicase, the RNA-directed RNA polymerase of bacteriophage Qβ, synthesizes by transcriptional slippage polyG strands, which on denaturing electrophoresis produce a ladder with at least three clusters of bolder bands. The ≈ 15-nt-long G , the major product of the shortest cluster, is tightly bound by the enzyme but can be released by the ribosomal protein S1, which, as a Qβ replicase subunit, normally promotes the release of a completed transcript.

View Article and Find Full Text PDF

The production of recombinant proteins in cells is often hampered by aggregation of newly synthesized proteins and formation of inclusion bodies. Here we propose the use of transverse urea gradient electrophoresis (TUGE) in testing the capability of folding of a recombinant protein from inclusion bodies dissolved in urea. A plasmid encoding the amino acid sequence 55-224 of TcpA pilin (C-terminal globular domain: TcpA-C) from El Tor enlarged by a His-tag on its N-terminus was expressed in cells.

View Article and Find Full Text PDF

SARS-CoV-2 is a rapidly evolving pathogen that has caused a global pandemic characterized by several consecutive waves. Based on epidemiological and NGS data, many different variants of SARS-CoV-2 were described and characterized since the original variant emerged in Wuhan in 2019. Notably, SARS-CoV-2 variants differ in transmissibility and pathogenicity in the human population, although the molecular basis for this difference is still debatable.

View Article and Find Full Text PDF

Isolation and Characterization of Two Novel Siphoviruses Novomoskovsk and Bolokhovo, Encoding Polysaccharide Depolymerases Active against .

Int J Mol Sci

October 2022

G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences, Federal Research Center, Prospect Nauki, 5, 142290 Pushchino, Russia.

This study describes two novel bacteriophages infecting members of the group. Even though members of the group are not recognized as pathogenic, several strains belonging to the group have been reported to cause infectious diseases in plants, animals and humans. group species are highly resistant to ultraviolet radiation and capable of forming biofilms, which complicates their eradication.

View Article and Find Full Text PDF

We present an update of EpiFactors, a manually curated database providing information about epigenetic regulators, their complexes, targets, and products which is openly accessible at http://epifactors.autosome.org.

View Article and Find Full Text PDF
Article Synopsis
  • - This study examined how 3β-corner super-secondary structures maintain their stability in water, independent of protein globules, using molecular dynamics (MD) simulations.
  • - Researchers analyzed various geometric parameters, like gyration radius and hydrogen bonds, and characterized a set of 3β-corner structures to show they consistently retained their formation.
  • - The findings suggest that 3β-corners are stable in aqueous environments and could serve as essential building blocks for protein folding and offer a standalone focus for structural biology research.
View Article and Find Full Text PDF
Article Synopsis
  • RAD51 is crucial for DNA repair and genome stability, and this study explores its amyloid properties in the context of bacterial curli-dependent amyloid generators (C-DAG).
  • The research employed various methods like polarized microscopy and transmission electron microscopy to confirm that purified human RAD51 forms detergent-resistant aggregates with a typical amyloid structure.
  • Observations included birefringence with Congo-red staining and distinct X-ray reflections, indicating that RAD51 possesses amyloid-like characteristics, which may have biological significance in cellular processes.
View Article and Find Full Text PDF

This article describes the clinical manifestation of natural infection in rainbow trout (Oncorhynchus mykiss) during an outbreak on a fish farm. (i) Using an integrated approach, we characterized the pathogenesis of vibriosis from the morphological, hematological, and biochemical points of view. The molecular mechanisms associated with the host immune response were investigated using mass spectrometric analysis of trout plasma proteins.

View Article and Find Full Text PDF

In this study, we conducted a comparative analysis of the structure of agonists and antagonists of transmembrane (TM) β-adrenoceptors (β-ARs) and their interactions with the β-ARs and proposed the mechanism of receptor activation. A characteristic feature of agonist and antagonist molecules is the presence of a hydrophobic head (most often, one or two aromatic rings) and a tail with a positively charged amino group. All β-adrenergic agonists have two carbon atoms between the aromatic ring of the head and the nitrogen atom of the amino group.

View Article and Find Full Text PDF

Y98 Mutation Leads to the Loss of RsfS Anti-Association Activity in .

Int J Mol Sci

September 2022

Department of Integrated Structural Biology, Institute of Genetics and Molecular and Cellular Biology, INSERM, U964, CNRS, UMR7104, University of Strasbourg, 67400 Illkirch Graffenstaden, France.

Article Synopsis
  • Ribosomal silencing factor S (RsfS) is a key protein that helps shut down ribosomes and supports cell survival during starvation, and is essential for the formation of the large ribosomal subunit.* -
  • RsfS inhibits the binding of the uL14 ribosomal protein to the large subunit, preventing it from joining with the small subunit.* -
  • Recent experiments identified critical amino acid Y98 on RsfS that could be a new target for drug development aimed at treating infections.*
View Article and Find Full Text PDF

The design of new protein variants is usually confined to slightly "fixing" an already existing protein, adapting it to certain conditions or to a new substrate. This is relatively easy to do if the fragment of the protein to be affected, such as the active site of the protein, is known. But what if you need to "fix" the stability of a protein or the rate of its native or intermediate state formation? Having studied a large number of protein mutant forms, we have established the effect of various amino acid substitutions on the energy landscape of the protein.

View Article and Find Full Text PDF
Article Synopsis
  • RimP is a crucial 17.7 kDa protein necessary for the maturation and efficient processing of the 30S ribosome's 16S rRNA, being involved in early assembly stages.
  • It helps stabilize the central pseudoknot during the initial steps of 30S subunit maturation, although the exact mechanism remains unclear.
  • The study details the chemical shift assignments of RimP from Staphylococcus aureus, revealing its structure, which includes eight β-strands and three α-helices, and aims to facilitate the discovery of selective inhibitors for bacterial translation.
View Article and Find Full Text PDF

Nowadays, progress in the determination of three-dimensional macromolecular structures from diffraction images is achieved partly at the cost of increasing data volumes. This is due to the deployment of modern high-speed, high-resolution detectors, the increased complexity and variety of crystallographic software, the use of extensive databases and high-performance computing. This limits what can be accomplished with personal, offline, computing equipment in terms of both productivity and maintainability.

View Article and Find Full Text PDF

ExuR and UxuR are paralogous proteins belonging to the GntR family of transcriptional regulators. Both are known to control hexuronic acid metabolism in a variety of Gammaproteobacteria but the relative impact of each of them is still unclear. Here, we apply 2D difference electrophoresis followed by mass-spectrometry to characterise the changes in the proteome in response to a or deletion.

View Article and Find Full Text PDF

Serine 339 of the active site of methionine γ-lyase (MGL) is a conserved amino acid in most pyridoxal 5'-phosphate-dependent enzymes of the cystathionine β-lyase subclass, to which MGL belongs. The reaction mechanism of the MGL-catalyzed γ-elimination reaction is poorly explored. We replaced serine 339 with alanine using site-directed mutagenesis.

View Article and Find Full Text PDF

The evaluation of temperature effects on the structure and function of enzymes is necessary to understand the mechanisms underlying their adaptation to a constantly changing environment. In the current study, we investigated the influence of temperature variation on the activity, structural dynamics, thermal inactivation and denaturation of and luciferases belonging to different subfamilies, as well as the role of sucrose in maintaining the enzymes functioning and stability. We used the stopped-flow technique, differential scanning calorimetry and molecular dynamics to study the activity, inactivation rate, denaturation and structural features of the enzymes under various temperatures.

View Article and Find Full Text PDF

Quite a long time ago, Oleg B. Ptitsyn put forward a hypothesis about the possible functional significance of the molten globule (MG) state for the functioning of proteins. MG is an intermediate between the unfolded and the native state of a protein.

View Article and Find Full Text PDF

How Can Ice Emerge at 0 °C?

Biomolecules

July 2022

Institute of Protein Research, Russian Academy of Sciences, 142290 Pushchino, Russia.

The classical nucleation theory shows that bulk water freezing does not occur at temperatures above ≈ -30 °C, and that at higher temperatures ice nucleation requires the presence of some ice-binding surfaces. The temperature and rate of ice nucleation depend on the size and level of complementarity between the atomic structure of these surfaces and various H-bond-rich/depleted crystal planes. In our experiments, the ice nucleation temperature was within a range from -8 °C to -15 °C for buffer and water in plastic test tubes.

View Article and Find Full Text PDF

The position weight matrix, also called the position-specific scoring matrix, is the commonly accepted model to quantify the specificity of transcription factor binding to DNA. Position weight matrices are used in thousands of projects and software tools in regulatory genomics, including computational prediction of the regulatory impact of single-nucleotide variants. Yet, recently Yan et al.

View Article and Find Full Text PDF

Solving the structures of bacterial, archaeal, and eukaryotic ribosomes by crystallography and cryo-electron microscopy has given an impetus for studying intracellular regulatory proteins affecting various stages of protein translation. Among them are ribosome hibernation factors, which have been actively investigated during the last decade. These factors are involved in the regulation of protein biosynthesis under stressful conditions.

View Article and Find Full Text PDF