Publications by authors named "I D Pokrovskaya"

Article Synopsis
  • The GARP complex is essential for anchoring endosome-derived vesicles to the trans-Golgi network, and its dysfunction leads to major trafficking and glycosylation problems.
  • Using a technique called mAID degron to quickly degrade VPS54 in human cells, researchers found that disrupting GARP resulted in the mislocalization and degradation of various Golgi proteins and early O-glycosylation abnormalities.
  • The study showed that GARP dysfunction causes vesicular coat mislocalization, builds up GARP-dependent vesicles, and affects specific proteins in the Golgi, highlighting its crucial role in cellular processes.
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Hemostasis, the process of normal physiological control of vascular damage, is fundamental to human life. We all suffer minor cuts and puncture wounds from time to time. In hemostasis, self-limiting platelet aggregation leads to the formation of a structured thrombus in which bleeding cessation comes from capping the hole from the outside.

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The Golgi is an essential eukaryotic organelle and a major place for protein sorting and glycosylation. Among apicomplexan parasites, retains the most developed Golgi structure and produces many glycosylated factors necessary for parasite survival. Despite its importance, Golgi function received little attention in the past.

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Platelets contribute to COVID-19 clinical manifestations, of which microclotting in the pulmonary vasculature has been a prominent symptom. To investigate the potential diagnostic contributions of overall platelet morphology and their α-granules and mitochondria to the understanding of platelet hyperactivation and micro-clotting, we undertook a 3D ultrastructural approach. Because differences might be small, we used the high-contrast, high-resolution technique of focused ion beam scanning EM (FIB-SEM) and employed deep learning computational methods to evaluate nearly 600 individual platelets and 30 000 included organelles within three healthy controls and three severely ill COVID-19 patients.

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Smith McCort (SMC) dysplasia is a rare, autosomal recessive, osteochondrodysplasia that can be caused by pathogenic variants in either or genes. These genes codes for proteins that are located at the Golgi apparatus and have a role in intracellular vesicle trafficking. We generated mice that carry a disease-causing variant, c.

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