Adenylate Cyclase

Adenylate cyclase is an enzyme that converts ATP into cyclic adenosine monophosphate (cAMP), a second messenger that relays signals inside cells. In many signaling pathways, ligand-activated G protein-coupled receptors stimulate or inhibit adenylate cyclase through G proteins, changing cAMP production; cAMP then activates protein kinase A and other effectors to alter cellular activity. This pathway helps regulate metabolism, gene expression, secretion, contraction, and sensory responses across diverse organisms. Studying adenylate cyclase clarifies how extracellular cues become intracellular responses and supports research on hormones, neurotransmitters, microbial signaling, and diseases involving disrupted signal transduction.

Adenylate Cyclase - Related Videos

Research

JoVE Journal - Bioengineering

Drug-induced Sensitization of Adenylyl Cyclase: Assay Streamlining and Miniaturization for Small Molecule and siRNA Screening Applications

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Cited by 6 •

2014

Persistent activation of inhibitory G protein-coupled receptors results in sensitization of adenylyl cyclase signaling. To identify the essential molecular pathways, nonbiased approaches are necessary; however, this strategy requires the development of a scalable cell-based cAMP sensitization assay. Herein, we describe a sensitization assay for small molecule and siRNA screening.

Real-Time Monitoring of Odorant Receptor Activation in Recombinant Cells

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2025

Source: de March, C. A. et. al., Real-time In Vitro Monitoring of Odorant Receptor Activation by an Odorant in the Vapor Phase. J. Vis. Exp. (2019)This video demonstrates the method to monitor the real-time activation of odorant receptors in recombinant mammalian cells using luminescence measurement. Odorant binding triggers G-protein activation and cAMP production, activating glosensor proteins that emit luminescence upon substrate binding, providing a quantitative measure of receptor response.

Research

JoVE Journal - Biochemistry
Free Sample

Investigating Protein Sequence-structure-dynamics Relationships with Bio3D-web

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Cited by 2 •

2017

A protocol for the online investigation of protein sequence-structure-dynamics relationships using Bio3D-web is presented.

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures

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Cited by 19 •

2016

Here, we describe settings to monitor in parallel circadian bioluminescence and the secretory activity of human islet cells and primary myotubes. For this, we employed lentiviral gene delivery of a luciferase core clock reporter, followed by in vitro synchronization and collection of outflow medium by continuous cell perifusion.

Research

JoVE Journal - Chemistry
Free Sample

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes

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Cited by 17 •

2016

Channels for the transportation of water molecules in enzymes influence active site solvation and catalysis. Herein we present a protocol for the engineering of these additional catalytic motifs based on in silico computer modeling and experiments. This will enhance our understanding of the influence of solvent dynamics on enzyme catalysis.

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