Chemical
Biology
including Bioinorganic Chemistry
Research Activities
The research activities in our laboratory involve organic/inorganic chemical synthesis, artificial enzymes including nanozymes, genetic code expansion and other multidisciplinary studies in the area of biomedical research. Our recent efforts are directed toward understanding the redox regulation by synthetic compounds in mammalian cells, thyroid hormone metabolism and thyroid related disorders, development of molecular probes for the detection and quantification of reactive oxygen species in the cells and oxidative stress biomarkers. We have a unique multidisciplinary team for an efficient collaboration within the laboratory and outside to undertake challenging contemporary research problems at the chemistry-biology interface.
Recent Publications
Vanadia Nanozymes Inhibit Platelet Aggregation, Modulate Signaling Pathways and Prevent Pulmonary Embolism in Mice
2025-05-11
Vanadia nanozymes with specific and morphology-dependent GPx activity effectively inhibit the aggregation of human platelets and prevent pulmonary thromboembolism in mice.
Angew. Chem. Int. Ed. 2025, 64, e202503737.
Effect of Halogen Substitution on the Regioselective Deiodination of Thyroid Hormone Analogues by Deiodinase Mimics
2025-02-03
The deiodination of thyroid hormones with peri-substituted naphthalene diselenol reveal that the regioselectivity towards iodine is not altered upon introduction of more electronegative halogens (F, Cl and Br), reinforcing the concept of halogen bonding in the deiodination reactions.
Chem. Eur. J. 2025, 31, e202404455.
Emerging Role of Noncovalent Interactions and Disulfide Bond Formation in the Cellular Uptake of Small Molecules and Proteins.
2025-01-20
The recent advances and the mechanistic aspects of intracellular delivery and role of non-covalent interactions during the cellular uptake of proteins and small molecules are described.
Chem. Asian J. 2025, 20, e202401734.
A Highly Selective Fluorescent Probe for Monitoring the Thyroid Hormone Transporter Activity in Mammalian Cells
2024-07-12
A highly selective fluorescent probe has been developed for monitoring thyroid hormone transporter activity in mammalian cells. The probe selectivity recognizes the monocarboxylate transporter 8 (MCT8) in various cell lines.
Chem. Eur. J. 2024, 30, e202401719
A Redox Modulatory SOD Mimetic Nanozyme Prevents the Formation of Cytotoxic Peroxynitrite and Improves Nitric Oxide Bioavailability in Human Endothelial Cells.
2023-07-28
The SOD mimetic CeVO4 nanozymes effectively regulate the bioavailability of both NO and superoxide, the two key constitutive molecules of vascular endothelium, even in the absence of the cellular SOD enzyme.
Adv. Healthcare Mater. 2023, 12, 202300621.
Antioxidant and Prooxidant Nanozymes: From Cellular Redox Regulation to Next-Generation Therapeutics.
2023-04-21
The advances in the development of redox-active nanozymes and their biomedical applications are described. We highlight the therapeutic significance of the antioxidant and prooxidant nanozymes in various diseases such as cancer, neurodegeneration, and cardiovascular diseases.
Angew. Chem. Int. Ed. 2023, 62, e202301232.
A Simple Substitution on Thyroid Hormones Remarkably Alters the Regioselectivity of Deiodination by a Deiodinase Mimic.
2022-11-15
The modulation of the electronic properties of the iodine atoms in thyroxine (T4) through the phenolic group has a remarkable influence on the regioselectivity of the deiodination.
Chem. Eur. J. 2023, 29, e202203111.
Cerium vanadate nanozyme with specific superoxide dismutase activity regulates mitochondrial function and ATP synthesis in neuronal cells.
2020-10-20
The first example of a nanozyme that can fully substitute the function of SOD1 and SOD2 in neuronal cells and regulate the synthesis of ATP under oxidative stress conditions is described.
Angew. Chem. Int. Ed. 2021, 60, 3121.
Modulation of Redox Signalling and Thiol Homeostasis in Red Blood Cells by Peroxiredoxin Mimetics.
2020-09-11
The first examples of selenium compounds that can prevent the oxidative stress-induced eryptosis by exhibiting an unusual Prx2-like redox activity under conditions when the cellular Prx2 and CAT enzymes are inhibited.