Publications by authors named "Liudmila I Kulikova"

Article Synopsis
  • - The study aims to advance the diagnosis and treatment of schizophrenia by identifying blood biomarkers, moving away from solely subjective assessments of clinical symptoms.
  • - Researchers conducted a detailed proteomic analysis of plasma samples from 48 schizophrenia patients and 50 healthy individuals, using advanced techniques to evaluate protein presence.
  • - Findings revealed unique proteins in schizophrenia patients that are linked to key biological processes, enhancing the understanding of the disorder's molecular mechanisms and potential therapeutic targets.
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The primary objective of analyzing the data obtained in a mass spectrometry-based proteomic experiment is peptide and protein identification, or correct assignment of the tandem mass spectrum to one amino acid sequence. Comparison of empirical fragment spectra with the theoretical predicted one or matching with the collected spectra library are commonly accepted strategies of proteins identification and defining of their amino acid sequences. Although these approaches are widely used and are appreciably efficient for the well-characterized model organisms or measured proteins, they cannot detect novel peptide sequences that have not been previously annotated or are rare.

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Proteomic and metabolomic research enables quantitation of the molecular profile of athletes. Multiomic profiling was conducted using plasma samples collected from 18 male athletes performing aerobic activity (running) at high altitude. Metabolomic profiling detected changes in the levels of 4-hydroxyproline, methionine, oxaloacetate, and tyrosine during the recovery period.

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Modification of the protein after synthesis (PTM) often affects protein function as supported by numerous studies. However, there is no consensus about the degree of structural protein changes after modification. For phosphorylation of serine, threonine, and tyrosine, which is a common PTM in the biology of living organisms, we consider topical issues related to changes in the geometric parameters of a protein (Rg, RMSD, C displacement, SASA).

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Article Synopsis
  • Researchers developed a new tool called SAFoldNet to improve the comparison and searching of 3D protein structures in structural biology.
  • SAFoldNet combines neural networks with the BLAST algorithm and uses a multistage process involving geometry conversion, candidate structure formation, and structural alignment refinement.
  • The tool's effectiveness was validated against current services, leading to a user-friendly web interface that allows for various protein structure analyses and provides similarity metrics.
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Amino acid substitutions and post-translational modifications (PTMs) play a crucial role in many cellular processes by directly affecting the structural and dynamic features of protein interaction. Despite their importance, the understanding of protein PTMs at the structural level is still largely incomplete. The Protein Data Bank contains a relatively small number of 3D structures having post-translational modifications.

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Article Synopsis
  • The study explores two types of protein structures, three-helix bundles and SH3-type barrels, across various organisms using a neural graph network to analyze their spatial folds.
  • Molecular experiments were conducted on small proteins with these structures, evaluating parameters like stability and structural integrity at different temperatures (300K, 340K, and 370K).
  • The research aims to show that it is possible to analyze these protein folds independently from their protein environment, leading to improved efficiency and reduced computation time without losing essential information.
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  • * Alpha-synuclein, which can aggregate and harm cells, interacts with cyclophilin A to prevent these destructive aggregations, highlighting the importance of chaperone proteins.
  • * Using advanced molecular docking techniques, we identified how alpha-synuclein, cyclophilin A, and Anle138b can form a stable complex, primarily through hydrophobic and hydrogen bonding interactions.
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A super-secondary structure (SSS) is a spatially unique ensemble of secondary structural elements that determine the three-dimensional shape of a protein and its function, rendering SSSs attractive as folding cores. Understanding known types of SSSs is important for developing a deeper understanding of the mechanisms of protein folding. Here, we propose a universal PSSNet machine-learning method for SSS recognition and segmentation.

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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.
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  • * JAK and STAT proteins play key roles in signaling processes related to inflammation and are important in autoimmune diseases like rheumatoid arthritis.
  • * The study explored how the drug ruxolitinib interacts with JAK1 and JAK2, showing it binds selectively to these proteins with strong binding affinities, mainly through hydrophobic interactions.
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  • Rheumatoid arthritis (RA) is a chronic autoimmune disease that causes joint damage and significant disability, largely driven by cytokines and the JAK/STAT signaling pathway.
  • The development of small molecule inhibitors targeting the JAK family has transformed RA treatment, with upadacitinib (Rinvoq) being a notable option due to its selectivity for JAK1 over JAK2 and JAK3.
  • Research indicates that the binding characteristics of upadacitinib with JAK1 through hydrogen bonds provide insights into its mechanism of action and how it differs among various JAK isoforms.
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  • Mass spectrometric profiling reveals the protein and metabolic composition of biological samples, but current computational methods struggle to accurately correlate spectra to molecular components, limiting its use in classifying diseases.
  • The study explores machine learning, specifically 1D and 3D convolutional neural networks (CNNs), to analyze raw mass spectrometry data directly for cancer classification, achieving a high accuracy of 0.95 in distinguishing between various cancer phenotypes and healthy individuals.
  • The neural networks demonstrated the ability to classify cancer types and assess their similarities, paving the way for more efficient identification of complex biological data without traditional preprocessing hurdles.
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Proteins expressed during the cell cycle determine cell function, topology, and responses to environmental influences. The development and improvement of experimental methods in the field of structural biology provide valuable information about the structure and functions of individual proteins. This work is devoted to the study of supersecondary structures of proteins and determination of their structural motifs, description of experimental methods for their detection, databases, and repositories for storage, as well as methods of molecular dynamics research.

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The association between cancer risk and schizophrenia is widely debated. Despite many epidemiological studies, there is still no strong evidence regarding the molecular basis for the comorbidity between these two pathological conditions. The vast majority of assays have been performed using clinical records of schizophrenic patients or those undergoing cancer treatment and monitored for sufficient time to find shared features between the considered conditions.

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