What fraction of estrogen receptors is expected to be free in the presence of an estradiol concentration of 1 nM assuming noother ligands are present? Enter your answer in decimal form.Fraction of free estrogen receptors: =0.9091Incorrect FeedbackXYou have not correctly determinedwhat fraction of estrogen receptors isexpected to be free in the presence ofan estradiol concentration of 1 nM. TheL1/2, the concentration of ligand atwhich half of the receptor is bound toligand and half is free, is approximately1 nM for estradiol. What fraction ofestrogen receptors are expected to befree when the concentration ofestradiol is equal to the L1/2?

Fractional saturation (Y) is the fraction of Receptors (R) that is bound by its Ligand (L). It can…

Answered: You have not correctly determined what…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Continuous exposure of a G protein-coupled receptor to its ligand leads to a phenomenon known as desensitization. Describe several molecule mechanisms for receptor desensitization
Ligand binding to proteins may occur with varying strengths; some ligands bind tightly to proteins while others bind less tightly. The strengths of reversible binding are determined experimentally by varying concentrations of ligands, and measuring the saturation of the protein in the various ligand concentrations. One such laboratory study investigated the binding of a hormone to three different receptor proteins in the cell membrane. The data collected are shown in the table below: 1) Provide a brief explanation as to why ligand binding to proteins must be a reversible process. 2) Calculate the dissociation constant (Kd) for the hormone binding to each of the three proteins.
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 explanation
Explain , What role does phosphorylation of tyrosine residues play in the action of receptor proteins?
You decide to investigate cell signaling of a pair of newly identified GPCRs, GPCR-W and GPCR-Z. Each binds the same ligand, but activates different downstream heterotrimeric G-proteins that act on adenylyl cyclase. You discover that ligand binding has opposite effects on adenylyl cyclase activity for each receptor. GPCR-W causes an increase in adenylyl cyclase activity, while GPCR-Z causes a decrease in adenylyl cyclase activity. You obtain a cell line expressing GPCR-W, GPCR-Z, the relevant G-proteins, and adenylyl cyclase. There is baseline adenylyl cyclase activity producing a baseline amount of cAMP. You embark on a research project to characterize the following mutations in the components of the signaling pathway. 2. Will each of the following mutations increase or decrease the levels of cAMP inside the cell upon adding the ligand to the cell culture? A mutation in Gi that prevents release of bound GDP. A mutation in Gs that prevents GTP hydrolysis. A mutation in Gi that…
From the Hill Plot below, the of the first binding event for the receptor-ligand system under study is: Q1 4nM Ο 10 μΜ -2 nM 2 nM Calculate the Hill Coefficient from the receptor-ligand binding data below: Q2 4 100 2 3 (0-1) 60 log 10 8 6 4 2 0 -2 -4 -6 -6 -4 -2 0 2 4 log [L] (nM) 6 8 10
Discuss the family of nuclear hormone receptors and explain how ligand binding to such a receptor can result in changes in gene expression
Select only one of these types of GPCR and describe the signal transduction that is involved in that receptor.
In Chapter 3, the Kd of calmodulin EF hands for binding Ca2+ is given as 10−6 M. Many proteins have much higher affinities for their respective ligands. Why is the specific affinity of calmodulin important for Ca2+ signaling pro- cesses such as that initiated by production of IP3?
2 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.
Steroid hormones are required by the body at puberty and into adolescence to regulate growth and cell division at more rapid pace than in later life. This regulation occurs via their interaction with cellular receptors and the signaling cascades/pathways that follow. Describe for me the difference between the two major classes of steroids, anabolic and catabolic steroids. What might you expect the result of signaling cascades to be in cells receiving either anabolic or catabolic “signals”? (B) At some point in late adolescence, steroid production decreases by almost 100 fold, as we transition into “adulthood”. Why might we wish to stop these signals from constantly being in our blood stream, (like, Say, between 17-24 years of age)? What result might these steroids have on cancer cells where abhorrent signaling is already causing an increased rate of cell division/growth? Could steroid use result in Cancer?
A fixed amount of radiolabelled insulin was incubated with a fixed amount of anti-insulin antibody, the bound ligand was separated from free ligand at different time intervals. Draw a diagram of the concentration of the insulin/antibody complex with time. (Insulin/antibody complex is the bound ligand) asap typed only .

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