Modelling of signalling via G-protein coupled receptors: Pathway-dependent agonist potency and efficacy
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作者:
Chen, CY
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Univ Nottingham, Sch Math Sci, Ctr Math Med, Div Theoret Mech, Nottingham NG7 2RD, EnglandUniv Nottingham, Sch Math Sci, Ctr Math Med, Div Theoret Mech, Nottingham NG7 2RD, England
Chen, CY
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Cordeaux, Y
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机构:Univ Nottingham, Sch Math Sci, Ctr Math Med, Div Theoret Mech, Nottingham NG7 2RD, England
Cordeaux, Y
Hill, SJ
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机构:Univ Nottingham, Sch Math Sci, Ctr Math Med, Div Theoret Mech, Nottingham NG7 2RD, England
Hill, SJ
King, JR
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机构:Univ Nottingham, Sch Math Sci, Ctr Math Med, Div Theoret Mech, Nottingham NG7 2RD, England
King, JR
机构:
[1] Univ Nottingham, Sch Math Sci, Ctr Math Med, Div Theoret Mech, Nottingham NG7 2RD, England
[2] Queens Med Ctr, Sch Med, Inst Cell Signalling, Nottingham NG7 2UH, England
[3] Queens Med Ctr, Sch Med, Sch Biomed Sci, Nottingham NG7 2UH, England
A mathematical model is constructed to study promiscuous coupling of receptors to G-proteins and to simulate events leading to the activation of multiple effector pathways within a cell. The model is directed at a better understanding of the factors that determine the efficacy and potency of a drug. Assuming that the receptors can exist in multiple conformational states, and allowing for agonist specific conformation, a system of ordinary differential equations is constructed and subsequently pathway-dependent agonist efficacy and potency order is predicted. A simple case of the compartmentalization of receptors and G-proteins is also given, using the current model to illustrate the effects of spatial heterogeneity on the predicted response. (C) 2003 Society for Mathematical Biology Published by Elsevier Ltd. All rights reserved.