drug binds to a receptor and causes an immediate change in the electrical signaling or excitability of that cell, without activating another signaling molecule. What type of receptor is this drug most likely binding to? G-protein coupled receptor (GPCR) Ligand-gated ion channel Enzyme-coupled receptor Intracellular receptor Voltage-gated ion channel

drug binds to a receptor and causes an immediate change in the electrical signaling or excitability of that cell, without activating another signaling molecule. What type of receptor is this drug most likely binding to? G-protein coupled receptor (GPCR) Ligand-gated ion channel Enzyme-coupled receptor Intracellular receptor Voltage-gated ion channel

Human Physiology: From Cells to Systems (MindTap Course List)

9th Edition

ISBN:9781285866932

Author:Lauralee Sherwood

Publisher:Lauralee Sherwood

Chapter4: Principles Of Neural And Hormonal Communication

Section4.5: Intercellular Communication And Signal Transduction

Problem 3CYU: Outline the three general means by which binding of a water soluble extracellular chemical messenger...

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Arrange the following in correct order in which G-protein coupled receptor systems are activated: Drug Receptor Protein kinase A Adenylyl cyclase G-protein Cellular response
Which of the following is the best description of how a G protein coupled receptor responds to a ligand binding? O Binding of ligand to the receptor causes the G protein to swap out GTP for GDP Binding of ligand to the receptor causes the G proteins to dimerize and trigger cross-phosphorylation Binding of ligand to the receptor causes the G protein to become activated, then the G protein travels through the plasma membrane to activate an enzyme Binding of ligand to the G protein triggers it to swap out GDP for GTP, causing it to become activated OOO O
Sort the following items based on which stage they are involved in: reception, transduction or response. Signaling molecule Receptor lyrosine kinase Protein synthesis G protein-coupled receptor cAMP Second messenger Ca2+ Phosphorylation cascade IP3 Adenylyl cyclase
The figure below shows a signaling pathway activated by the bindiıng of adrehalMNe LU the beta-adrenergic receptor. Binding of adrenaline to the receptor causes GTP-binding and activation of G proteins. Active GTP-bound G protein activates adenylate cyclase to initiate a signaling cascade that affects cellular responses, and includes cellular changes to mediate increased heart rate and accounts for the flight-or-fight response. activated adenylate cyclase adrenaline activated B-adrenergic receptor adenylate cyclase G protein subunit 22 GTP SDP conformational ATP CAMP change in receptor heterotrimeric G protein ACAMP inactive protein kinase A active protein kinase A 4 cellular responses Consider the homozygous mutation in which a cell produces a variant of adenylate cyclase that can no longer be activated Which of the following are true in this cell? Select all that apply. Heart rate increases Protein Kinase A is not activated CAMP levels are lower than normal Heart rate decreases
Which of the following statements most accurately describes what happens when an antagonist binds to a receptor? The antagonist binds non-covalently to the receptor and promotes internalisation of the receptor. Antagonist binding alters the structure of the receptor making it unable to function normally. At sufficiently high concentrations the antagonist can prevent the receptor from binding to its natural (endogenous) ligand. The antagonist-receptor complex binds to a heterotrimeric G protein forming a stable and inactive ternary complex.
Compare and contrast signaling via G-protein coupled receptor, receptor tyrosine kinases, nuclear receptor. Please name at least one ligand/receptor for each pathway. Also describe the 'fast' and 'slow' responses mediated by ligand binding
G protein-coupled receptors bind extracellular signals then activates trimeric G proteins inside the cell. Based on this information, which of the following statements best characterizes G protein- coupled receptors? O It is peripheral and monolayer associated O It is integral and transmembrane O It is peripheral and transmembrane O Itis integral and monolayer associated
Name three features common to the activation of cytokine receptors and receptor tyrosine kinases. Name one difference with respect to the enzyme activity of these receptors.
The figure below shows a signaling pathway activated by the binding of adrenaline to the beta-adrenergic receptor. Binding of adrenaline to the receptor causes GTP-binding and activation of G proteins. Active GTP-boundG protein activates adenylate cyclase to initiate a signaling cascade that affects cellular responses, and includes cellular changes to mediate increased heart rate and accounts for the flight-or-fight response. activated adrenaline activated B-adrenergic receptor adenylate cyclase adenylate cyclase G protein subunit GTP 3. GDP conformational ATP CAMP change in receptor heterotrimeric G protein ACAMP inactive protein kinase A active protein kinase A cellular responses Consider the homozygous mutation in which a cell produces a variant of the adrenergic receptor that is constitutively active in the absence of ligand. Which of the following are true in this cell? Select all that apply. Protein Kinase A is always activated CAMP concentration is higher than normal Heart rate…
List the ions that contribute to electrical signaling in neurons and what side of the neuron their concentration is highest
Which of the following is most likely an example of signaling through a transmembrane receptor? The influenza virus recognizes specific proteins on the surface of host cells, causing the entrance of genetic materials into the cytoplasm of the host cells. Low-density lipoproteins (LDL) bind to receptor proteins found on the membrane of receiving cells, triggering its internalization into the receiving cells. The binding of interleukin-6 (IL-6) to the interleukin-6 receptor causes the activation of protein kinases in the cytoplasm, activating the transcription factor NF-κB. The binding of aldosterone to the aldosterone receptor activates its transcription activity, leading to the transcription of genes that promote the uptake of ions and water.
In the B-acrenergic receptor signaling pathway where desensitization occurs, what protein acts as an effector protein? The activity of the effector protein directly affects the activity of which protein in this pathway? How would the presence of a GAP affect the desensitization process? stimulate it inhibit it have no effect What is the actual mechanism by which desensitization occurs? the receptor is ubiquitinated the hormone is phosphorylated the hormone is degraded the receptor is internalized