Orcid Publication

Detalle de: Perspectives on TRPV Channels in the Structural and Computational Revolution Era

Title Perspectives on TRPV Channels in the Structural and Computational Revolution Era
Abstract

Transient Receptor Potential Vanilloid (TRPV) channels are a subfamily of six membrane proteins involved in various physiological processes. TRPVs share a pore channel between the fifth and sixth domains, which can be activated or inactivated by temperature, pain, and cellular homeostasis. Dysregulation of TRPVs can lead to pain, inflammation, and numerous pathological conditions. Understanding the molecular mechanisms that control TRPV channel activation/inhibition, gating, and interactions with ligands is crucial for targeted drug design. Molecular dynamics (MD) simulations have emerged as a powerful computational tool to study TRPVs' function and ligand interaction. In this chapter, we review the use of MD and other computational tools to investigate the function and gating mechanism of TRPVs, as well as the binding of lipids and small molecules in these channels. In short, we describe the changes induced by channel opening caused by temperature and upon ligand or lipid binding. Furthermore, we review the studies that delve into describing binding sites or discovering new TRPV channel modulators.

Apa Reference Catalina-Hernandez, E., López-Martín, M. & Peralvarez-Marin, A. (2026). Perspectives on TRPV Channels in the Structural and Computational Revolution Era. Advances in Experimental Medicine and Biology, 259-285. 10.1007/978-3-032-07523-9_10
Doi 10.1007/978-3-032-07523-9_10
Publication Date 2026
Publication Type Book / chapter
Ontology Computational models and simulations, Biomolecular simulation, Drug Discovery and design, Molecular Interactions/Docking
Researchers Mario López Martín
Research Groups
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