The dissociation constant (Kd) of a receptor is:
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Q: The dissociation constant (Kd) of a receptor is: BIOCHEMISTRY basic the concentration of a…
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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.
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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…A ligand binds two different receptors with a Kd value of 10−7 M for receptor 1 and a Kd value of 10−9 M for receptor 2. For which receptor does the ligand show the greater affinity? Calculate the fraction of receptors that have a bound ligand ([RL]/RT) in the case of receptor 1 and receptor 2 if the con- centration of free ligand is 10−8 M.Can you please explain me the following: regulation of receptors: homologous and heterologous receptor desensitization, receptor internalization and trafficking, receptor down-regulation
- 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.Explain whether the specificity of interaction will be high or low for each given situation. a. The value of KD of the ligand's interaction to the target receptor is very much lower than the value of KD of the ligand's interaction to off-targets. b. The ligand concentration [L] is higher than the KD value of its interaction with the target and the KD value of its interaction to off-targets.Choose the best term which describe the following statement: antagonist binds to the binding site of receptor and change the shape: Select one: Incorrect Induced fit. Correct induced fit. Signal transduction. Perfect fit.
- Explain why a peptide (protein) ligand can’t use a receptor inside the cell while an asteroid has no problem using an intracellular receptor.when a chemical messenger (or ligand) reaches a target cell, it binds to a receptor. A hydrophobic ligand binds to a(n) _______, whereas a hydrophilic ligand binds to a(n)_________. a. agonist receptor; antagonic receptor b. transmembrane receptor; intracellular receptor c. antagonist receptor; agonist receptor d. intracellular receptor; transmembrane receptorExplain whether the specificity of interaction will be high or low for each given situation. a. The concentration of the ligand's complex to the target receptor equates to the concentration of the ligand's complex to off-targets. b. The target receptor's total concentration is very much higher than the off-target's total concentration.
- When comparing two or more ligands, a larger numerical value for KD corresponds to a higher binding affinity. True False In radioligand binding assays, a large excess of a noncompetitive antagonist is used to determine the specific binding of the radiolabeled ligand. True False Exocrine glands have ducts that provide a passageway for secretions to move to the surface of the epithelium. True False An inverse agonist binds to a receptor with an affinity that is inversely proportional to its potency. True False Can I get the answer? I don't need explanationThe top panel (a) of this figure shows the graded potential change (far right, upper, electrical trace) that results from ligand binding to the ligand gated Na+ channel. The bottom panel of this figure (b) shows a graded potential change (far right, lower, electrical trace) that results from ligand binding to a ligand gated Cl- channel. From this trace you know (Vm = -70 mV) 1. ECl- is -70 mV 2. ECl- is more negative than -70 mV (i.e., -80 mV) 3. ECl- is more positive than -70 mV (i.e., -60 mV)Which of the following statements best defines the term ‘spare receptors’? ‘Spare receptors’ refers to receptors that are broken down by cells because they are surplus to requirements. ‘Spare receptors’ occur when the KD for agonist binding to the receptor is smaller than the EC50 determined for a particular physiological response. ‘Spare receptors’ refers to the pool of intracellular receptors that are able to translocate to the plasma membrane. ‘Spare receptors’ can be defined as the number of receptors not occupied by agonist when a maximal response has been achieved, compared to the total number of receptors in the cell.