Olfr825 is an olfactory receptor belonging to the G protein-coupled receptor (GPCR) family, specialized in detecting a variety of odorant molecules. These receptors are pivotal in the process of olfaction, translating chemical stimuli into neural signals that are perceived as scents by the brain. Olfr825, like other olfactory receptors, is embedded in the olfactory epithelium and plays a crucial role in the detection and discrimination of odorants. The mechanism of activation for Olfr825 involves the direct binding of specific chemical compounds, which are odorants, to the receptor. This interaction results in a conformational change in Olfr825, a critical step in triggering the olfactory signaling cascade. Upon binding of an odorant molecule, Olfr825 undergoes a structural alteration that enables it to activate an associated G protein. The activated G protein then stimulates adenylate cyclase, leading to an increase in the intracellular concentration of cyclic AMP (cAMP). Elevated cAMP levels result in the activation of protein kinase A (PKA), which phosphorylates various targets within the cell. This cascade of events culminates in the opening of ion channels, particularly calcium and sodium channels, leading to depolarization of the olfactory sensory neuron. This depolarization generates an electrical signal that is transmitted to the brain, where it is interpreted as a specific smell.
The chemicals listed in the table have been selected for their potential to directly bind and activate Olfr825. Their structural compatibility with the receptor's binding site allows them to act as effective activators, triggering the receptor's conformational change and subsequent signal transduction. The specificity of this interaction is essential for the selective and precise perception of odors. This direct activation of Olfr825 by these odorants demonstrates the intricate nature of olfactory receptor-ligand interactions, which are fundamental to the sense of smell and the ability to discern a wide range of aromatic compounds.
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