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Vitecek, J.

Publications and source records attributed to Vitecek, J..

3 recordsLinked to original sources

Fibrin Selective Alteplase with Improved Thrombolysis and Inhibition Resistance Engineered by Rational Design

Thrombolytic enzymes represent an important class of proteolytic biocatalysts for medical applications, yet currently used FDA-approved variants, including alteplase and tenecteplase, remain limited by suboptimal catalytic efficiency, off-target activity, and susceptibility to inhibition. These limitations reflect the complexity of enzyme function in physiological environments, where therapeutic performance depends on the simultaneous optimization of multiple catalytic and biophysical properties. Here, we introduce a multi-objective enzyme engineering strategy for the design of next-generation thrombolytic proteases, explicitly targeting multiple properties required for therapeutic performance. Our approach combines computer-aided design, evolutionary reconstruction, and literature-guided mutation selection to improve catalytic activity, fibrin selectivity, inhibition resistance, and functional lifetime within a single workflow. This framework is coupled with systematic biochemical characterization, in vitro evaluation of clot penetration and fibrinolytic activity, and in vivo validation of efficacy and safety. By addressing multiple performance parameters simultaneously, this strategy enables efficient navigation of trade-offs that typically limit enzyme optimization. Using this approach, we identify Brnoteplase as a lead variant with enhanced fibrin selectivity, improved resistance to inhibition, and superior clot penetration, resulting in increased effective catalytic lifetime and enabling bolus administration. In vivo studies demonstrate enhanced thrombolysis and recanalization with reduced hemorrhagic complications. These findings provide a broadly applicable framework for designing proteolytic biocatalysts suitable for complex biological environments.

biochemistry↗

Biochemical and Immunological Properties of Engineered Low-Immunogenic Staphylokinases for Next-Generation Thrombolytic Therapy

Staphylokinase (SAK) is a highly fibrin-specific plasminogen activator with significant potential as a safe and affordable thrombolytic. Yet, its clinical translation can be limited by potential immunogenicity. To accelerate the development of improved thrombolytics, a critical step is identifying the most suitable molecular template. Therefore, we performed a comparative analysis of biochemical and immunological properties of three engineered low-immunogenic variants (SAK SY155, SAK THR174, and SAK STAR FRIDA) and two wild-types (SAK STAR and SAK 42D), using a newly established panel of assays. All variants retained potent thrombolytic activity, with SAK SY155 displaying the highest catalytic efficiency and fibrin-clot permeability. However, this advantage did not fully translate into improved clot reduction under flow conditions. Comprehensive immunological profiling, including T lymphocyte proliferation, dendritic cell maturation, mouse immunization models, and human serum reactivity tests, confirmed decreased immunogenicity for two low-immunogenic variants. Overall, low-immunogenic SAK SY155 emerged as the most promising template for rational engineering of next-generation thrombolytics.

biochemistry↗

Exploring the Role of PEDOT Electrodes in Electrostimulation of vascular endothelial cells

The potential of electrical stimulation for cell control in tissue engineering remains largely underestimated, as does the use of organic semiconductors. The tunable physico-chemical properties of organic semiconductors offer advantages over commonly used inert metals. This study investigates the effects of pulsed electrostimulation and electrode materials, gold and poly(3,4-ethylenedioxythiophene) (PEDOT), on the physiological functionality of human vascular endothelial cells. A novel electrostimulation platform incorporating gold or PEDOT electrodes was developed and characterized for electrical performance. Human umbilical vein endothelial cells were cultured on this platform, and the effects of electrostimulation and electrode material were assessed through morphological analysis, nitric oxide (NO) production, and expression of key endothelial marker genes. PEDOT electrodes produced higher electrical current during electrostimulation. Interestingly, cell morphology, including elongation and alignment, showed minimal changes under electrostimulation. NO production, a key marker of vascular health, was enhanced by electrostimulation, with PEDOT electrodes showing a trend toward greater NO accumulation than gold. Gene expression analysis revealed material- and stimulation-specific trends: electrostimulation generally upregulated KLF2, KLF4, and CYP1B1 on PEDOT electrodes but suppressed their expression on gold electrodes. These findings suggest that PEDOT electrodes, with their enhanced electrochemical properties and ability to support endothelial functionality, provide a safe and efficient platform for endothelial cell electrostimulation. This study advances understanding of the interplay between material properties and electrostimulation and highlights PEDOT as a promising candidate for vascular tissue engineering and regenerative medicine.

cell biology↗