The following graph shows the AMPA/NMDA ratio in cells from rats that were either: naive, unpaired or paired in an associative learning task. The increase in the paired condition is most likely due to: AMPA/NMDA 654321 Naive Unpaired Paired 4 O AMPA and NMDA receptor insertion into the membrane O NMDA receptor insertion into the membrane O Signaling through metabotropic receptors O AMPA receptor insertion into the membrane
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- You can choose one or more than one option The dissociation constant (Kd) of a receptor is: BIOCHEMISTRY basic the concentration of a ligand that produces 100% occupancy of the receptor the concentration of a ligand that produces 50% of the maximal effect. the measurement of specificity between ligand and its receptor. the measurement of speed by which a ligand will dissociate from its receptor. the measurement of affinity between a ligand and its receptor and the inverse of the association constant. During an experiment with Drosophila, it was discovered that all females had red eyes. unlike males. A conclusion based on this observation would be: MOLECULAR BIOLOGY basic The gene for eye color is located on the X chromosome. The females are homozygotes The gene for eye color is dominant. The eye color results from multigenic linkage. The eye color phenotype is sex-linked A secondary lysosome: CELL BIOLOGY advanced a lysosome that provides a backup to the primary…You can choose one or more than one option The dissociation constant (Kd) of a receptor is: the concentration of a ligand that produces 100% occupancy of the receptor the concentration of a ligand that produces 50% of the maximal effect. the measurement of specificity between ligand and its receptor. the measurement of speed by which a ligand will dissociate from its receptor. the measurement of affinity between a ligand and its receptor and the inverse of the association constant.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.
- added ligand concentration of 10 µM is 5 × 10³ s¹. What is the value of the reverse rate constant k_1 = 1 ×10-4 Incorrect Macmillan Learning You have not correctly calculated the value of the reverse rate constant. To begin, calculate the value of k₁ by dividing the rate of receptor-ligand complex formation (the rate of the forward reaction) by the ligand concentration. k₁ = rate forward [L] Then, calculate the value of the reverse rate constant, k_₁, by multiplying the dissociation constant, Kd, and the forward rate constant, k₁. k_1 = Kak₁Based on our discussions for different members of the K+ channel family (which include Kv, KCa, HCN/CNG, Kir, and K2P), which of the following can bind to K+ channels, enhancing activation? Ca++/calmodulin Cyclic nucleotides (cAMP, cGMP) PIP2 All of the above2 of 16 Compound Binds to Elicits biological receptor response A Yes Yes B Yes No C No No Refer to the table above. Compound X is the natural ligand that binds to a receptor and stimulates a signal transduction pathway associated with the receptor. Based on the information given in the table, what are the roles of compounds A, B, and C? O A is an antagonist, B is an agonist, and C is a ligand. A is an agonist, B is an antagonist, and C has no role. A is a ligand, B has no role, and C is an antagonist. A is an agonist, B is an antagonist, and C is an agonist. A has no role, B is an agonist, and C is an antagonist.
- Which statement best describes the interaction that occurs as a result of the binding of a ligand to a ligand-gated ion channel receptor? A B с D ligand extracellular environment gate closed inactive ligand-gated ion channel receptor ions The process permanently opens or closes the ion channel. cytoplasm The process alters the membrane potential by changing the intracellular ionic concentration. The process causes G proteins to bind with GTP and become activated. The process removes three sodium ions from the cell and brings in two potassium ions.you have been asked to develop a drug that could inhibit an enzyme linked receptor. what are the potential pharmacological targets you could design your drug to interact with. which one should you choose and whyBriefly explain the difference between a receptor antagonist and a receptor inverse agonist. Describe both the resulting receptor conformation as well as the signal transduction.
- The figure below illustrates a model of a signal transduction cascade, initiated by the bind- ing of a ligand to a membrane-bound receptor. ligand A partial model of a signal transduction pathway A inactivated molecules B -receptor protein A D activated molecule 1 Based on the figure, which of the following describes the most likely outcome of a mutation that changes the intracellular region of receptor protein A? activated molecule 2 activated molecule 3 The receptor will not activate molecule 1, but the activation of molecules 2 and 3 will continue at lower rates. Molecule 1 will not become activated, preventing the activation of molecules 2 and 3 and the subsequent cellular response. с The ligand will not be able to bind the membrane-bound receptor, preventing the signal transduction pathway from initiating. The ligand that binds to protein A will not enter the cell, preventing the cellular response from occurring.From the Hill Plot below, the KD of the first binding event for the receptor-ligand system under study is: 10 8 6 4 2 0 -2 4 6 8 10 (0=1) 601 log -4- -6 -6 -4 -2 0 2Which 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.