Publications by authors named "V A Arkhipova"

The adenosine triphosphate (ATP)-binding cassette (ABC) importer GlnPQ from has two sequential covalently linked substrate-binding domains (SBDs), which capture the substrates and deliver them to the translocon. The two SBDs differ in their ligand specificities, binding affinities and the distance to the transmembrane domain; interestingly, both SBDs can bind their ligands simultaneously without affecting each other. In this work, we studied the binding of ligands to both SBDs using X-ray crystallography and molecular dynamics simulations.

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Immunohistochemical detection of the LYVE-1 marker in healthy human full-thickness skin (the epidermis and the dermis) was carried out. LYVE-1 expression was found in the endothelium of lymphatic capillaries located in the papillary dermis, in the endothelium of larger lymphatic vessels of the reticular dermis, and in fibroblasts, which indicates their joint participation in hyaluronan metabolism. LYVE-1 staining detected for the first time in cells of the stratum basale, the stratum spinosum, and the stratum granulosum of healthy human epidermis indicates their participation in hyaluronan metabolism and allows us to consider the spaces between epidermis cells as prelimphatics.

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Background And Objectives: The use of ablative fractional lasers to enhance the delivery of topical drugs through the skin is known as laser-assisted drug delivery. Here, we compare a novel 3050/3200 nm difference frequency generation (DFG) fiber laser (spot size: 40 µm) to a commercially used CO laser (spot size: 120 µm). The objective is to determine whether differences in spot size and coagulation zone (CZ) thickness influence drug uptake.

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Article Synopsis
  • Researchers have struggled to determine the exact structure of SARS-CoV-2, particularly its envelope which protects the viral RNA and contains key proteins.
  • The study utilizes advanced computational modeling to analyze the dynamic interactions of the underexplored membrane (M) protein, revealing that M proteins can form large, filament-like structures.
  • Findings from molecular dynamics simulations confirm the stability of the envelope and align with existing experimental data, showcasing a new method for modeling viral structures from scratch.
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  • Short regulatory oligonucleotides, like microRNAs, are promising for immunotherapy but need effective carriers to enter immune cells.
  • This study examines the use of polycationic dendrimers as delivery vehicles for a microRNA inhibitor targeting miR-155 in immune cells from healthy donors.
  • The dendrimer-microRNA complexes improved the regulation of specific immune cell populations and influenced certain immune responses, hinting at their potential usefulness in immunotherapy while also indicating room for enhancement in targeting immune cell subsets.
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