Askar D. Turashev
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Askar D. Turashev has a total of 26 co-authors. Here are the top co-authors by number of shared publications:
- Alexander V. Maksimenko
Ministry of Health of the Russian Federation
3 shared publications - A. S. Esman
Central Research Institute of Epidemiology
1 shared publication - Anna Golubeva
Central Research Institute of Epidemiology, Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing Russian Federation, 3a Novogireevskaya Str., 111123 Moscow, Russia
1 shared publication - Anna K. Keshek
Enikolopov Institute of Synthetic Polymeric Materials of Russian Academy of Sciences, Profsoyuznaya Str. 70, 117393 Moscow, Russia
1 shared publication Anna S. But
The Pacific Institute of Bioorganic Chemistry, Russian Academy of Sciences, 690 022 Vladivostok, Russia
1 shared publication- Anna S. Cherkashina
Central Research Institute of Epidemiology, Moscow 111123, Russia
1 shared publication
Latest Publications
- Open Access
- 29 October 2026
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (21) , 9711
Simple, Fast and Cheap Pb2+ and Hg2+ Detection in Liquid Media Using EGOFET-Based Aptasensors
Lead and mercury are among the most dangerous environmental pollutants due to their high toxicity to humans and other living organisms. They are also ubiquitous in our ecosystems as a result of industrial waste. Therefore, it is essential to develop a simple and inexpensive method to rapidly detect low concentrations of these metals in various liquids, including wastewater. Aptamer-based electrolyte-gated organic field-effect transistors (EGOFETs), which are traditionally used to detect large biomolecules such as viruses and proteins, are a promising concept for heavy-metal detection. To achieve this, we chose several aptamers with high affinity for and specificity to Pb2+ and Hg2+ ions, determined the dissociation constants and stoichiometry of the complexes, investigated the kinetics of complex formation and cross-specificity and proposed structures for the aptamer–cation complexes. Based on these aptamers, we developed EGOFET-based aptasensors for Pb2+ and Hg2+. The fabricated EGOFET devices have been shown to be sensitive to low concentrations of lead (from 30 nM to 2.5 μM) and mercury (from 250 nM to 2.5 μM) cations. These ranges correspond to the maximum permissible concentrations in drinking and wastewater for lead, which are 144 nM and 1.2 μM, respectively, and exceed the range of maximum permissible concentration in drinking and wastewater for mercury, which is 5 nM. Despite this, it was possible to detect mercury cations at a concentration of 5 nM within five minutes in a model system that simulates liquid flow using the EGOFET device. This demonstrates the potential for fast and selective detection of Pb2+ and Hg2+ ions at maximum permissible concentrations in drinking water using EGOFET-based aptasensors. This is a significant step forward in the development of flow sensors for detecting heavy metals in liquid media.
- 29 October 2026
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (21) , 9711
Open AccessSimple, Fast and Cheap Pb2+ and Hg2+ Detection in Liquid Media Using EGOFET-Based Aptasensors
Lead and mercury are among the most dangerous environmental pollutants due to their high toxicity to humans and other living organisms. They are also ubiquitous in our ecosystems as a result of industrial waste. Therefore, it is essential to develop a simple and inexpensive method to rapidly detect low concentrations of these metals in various liquids, including wastewater. Aptamer-based electrolyte-gated organic field-effect transistors (EGOFETs), which are traditionally used to detect large biomolecules such as viruses and proteins, are a promising concept for heavy-metal detection. To achieve this, we chose several aptamers with high affinity for and specificity to Pb2+ and Hg2+ ions, determined the dissociation constants and stoichiometry of the complexes, investigated the kinetics of complex formation and cross-specificity and proposed structures for the aptamer–cation complexes. Based on these aptamers, we developed EGOFET-based aptasensors for Pb2+ and Hg2+. The fabricated EGOFET devices have been shown to be sensitive to low concentrations of lead (from 30 nM to 2.5 μM) and mercury (from 250 nM to 2.5 μM) cations. These ranges correspond to the maximum permissible concentrations in drinking and wastewater for lead, which are 144 nM and 1.2 μM, respectively, and exceed the range of maximum permissible concentration in drinking and wastewater for mercury, which is 5 nM. Despite this, it was possible to detect mercury cations at a concentration of 5 nM within five minutes in a model system that simulates liquid flow using the EGOFET device. This demonstrates the potential for fast and selective detection of Pb2+ and Hg2+ ions at maximum permissible concentrations in drinking water using EGOFET-based aptasensors. This is a significant step forward in the development of flow sensors for detecting heavy metals in liquid media.
- Open Access
Development and Application of Real-Time PCR-Based Screening for Identification of Omicron SARS-CoV-2 Variant Sublineages
The Omicron strain is currently the main dominant variant of SARS-CoV-2, with a large number of sublineages. In this article, we present our experience in tracing it in Russia using molecular diagnostic methods. For this purpose, different approaches were used; for example, we developed multiprimer panels for RT-PCR and Sanger and NGS sequencing methods. For the centralized collection and analysis of samples, the VGARus database was developed, which currently includes more than 300,000 viral sequences.
Open AccessDevelopment and Application of Real-Time PCR-Based Screening for Identification of Omicron SARS-CoV-2 Variant Sublineages
The Omicron strain is currently the main dominant variant of SARS-CoV-2, with a large number of sublineages. In this article, we present our experience in tracing it in Russia using molecular diagnostic methods. For this purpose, different approaches were used; for example, we developed multiprimer panels for RT-PCR and Sanger and NGS sequencing methods. For the centralized collection and analysis of samples, the VGARus database was developed, which currently includes more than 300,000 viral sequences.
- 26 March 2014
- Published by Pleiades Publishing Ltd in Russian Journal of Bioorganic Chemistry
- Vol. 40 (2) , 119-128
Endothelial glycocalyx of blood circulation system. I. Detection, components, and structural organization
The luminal surface of a blood vessel accommodates a complex multicomponent system of mainly carbohydrates and proteins called glycocalyx. According to the concept of the double protective layer, glycocalyx is the first protection barrier of the vascular wall. The structure of glycocalyx is determined by a group of proteoglycans, glycoproteins, and glycosaminoglycans. Two groups of molecules are distinguished within the glycocalyx constituents, that is, membrane proteoglycans (syndecans and glypicans bound to endothelial cell membranes) and soluble proteoglycans (perlecan, biglycan, versican, decorin, and mimecan). There are five types of glycosaminoglycan chains; these are heperan sulfate, chondroitin sulfate, dermatan sulfate, keratan sulfate, and hyaluronan. There is a dynamic equilibrium between the soluble components of glycocalyx and flowing blood, which allows for separation of the endothelial surface layer. Due to its complexity and location at the interface of blood circulation system, glycocalyx is involved in the maintenance of vascular homeostasis. Here, the molecular composition of glycocalyx, properties of its components, biosynthesis, and common structural features are discussed.
- 26 March 2014
- Published by Pleiades Publishing Ltd in Russian Journal of Bioorganic Chemistry
- Vol. 40 (2) , 119-128
Endothelial glycocalyx of blood circulation system. I. Detection, components, and structural organization
The luminal surface of a blood vessel accommodates a complex multicomponent system of mainly carbohydrates and proteins called glycocalyx. According to the concept of the double protective layer, glycocalyx is the first protection barrier of the vascular wall. The structure of glycocalyx is determined by a group of proteoglycans, glycoproteins, and glycosaminoglycans. Two groups of molecules are distinguished within the glycocalyx constituents, that is, membrane proteoglycans (syndecans and glypicans bound to endothelial cell membranes) and soluble proteoglycans (perlecan, biglycan, versican, decorin, and mimecan). There are five types of glycosaminoglycan chains; these are heperan sulfate, chondroitin sulfate, dermatan sulfate, keratan sulfate, and hyaluronan. There is a dynamic equilibrium between the soluble components of glycocalyx and flowing blood, which allows for separation of the endothelial surface layer. Due to its complexity and location at the interface of blood circulation system, glycocalyx is involved in the maintenance of vascular homeostasis. Here, the molecular composition of glycocalyx, properties of its components, biosynthesis, and common structural features are discussed.
- Open Access
- 29 November 2011
- Published by Wiley in Biochemistry Research International
- Vol. 2012, 1-10
No-Reflow Phenomenon and Endothelial Glycocalyx of Microcirculation
The progress in reperfusion therapy dictated the necessity for developing new tools and procedures for adjacent/additional therapy of acute cardiovascular disorders. The adjacent therapy is targeted on the damage of the microcirculation, leading to the unfavorable prognosis for the patients. The no-reflow phenomenon holds special place in the multifactorial etiology of the microcirculation disorders, offering a new challenge in treating the patients associated with ST-segment elevation on ECG at myocardial infarction. One of the numerous causes of no-reflow, the influence of the endothelial glycocalyx of the microcirculation, is analyzed. The results obtained in the studies of the endothelial glycocalyx ultrastructure are generalized, the effect that the fragments of the glycocalyx glycosaminoglycans have on the function of the vascular wall is demonstrated. The trends in searching for correlations between the thickness of the capillary glycocalyx and the cardiovascular disease risk are noted.
- 29 November 2011
- Published by Wiley in Biochemistry Research International
- Vol. 2012, 1-10
Open AccessNo-Reflow Phenomenon and Endothelial Glycocalyx of Microcirculation
The progress in reperfusion therapy dictated the necessity for developing new tools and procedures for adjacent/additional therapy of acute cardiovascular disorders. The adjacent therapy is targeted on the damage of the microcirculation, leading to the unfavorable prognosis for the patients. The no-reflow phenomenon holds special place in the multifactorial etiology of the microcirculation disorders, offering a new challenge in treating the patients associated with ST-segment elevation on ECG at myocardial infarction. One of the numerous causes of no-reflow, the influence of the endothelial glycocalyx of the microcirculation, is analyzed. The results obtained in the studies of the endothelial glycocalyx ultrastructure are generalized, the effect that the fragments of the glycocalyx glycosaminoglycans have on the function of the vascular wall is demonstrated. The trends in searching for correlations between the thickness of the capillary glycocalyx and the cardiovascular disease risk are noted.
- 31 October 2008
- Published by Elsevier in Journal of Biotechnology
- Vol. 136, S202-202
Glycation of hyaluronidase by mono- and di-saccharides: Protective effect of chondroitin sulfate microenvironment in vitro and in silico
- 31 October 2008
- Published by Elsevier in Journal of Biotechnology
- Vol. 136, S202-202
Glycation of hyaluronidase by mono- and di-saccharides: Protective effect of chondroitin sulfate microenvironment in vitro and in silico