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2017 ; 5
(3
): e00311
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A three-parameter two-state model of receptor function that incorporates
affinity, efficacy, and signal amplification
#MMPMID28603630
Buchwald P
Pharmacol Res Perspect
2017[Jun]; 5
(3
): e00311
PMID28603630
show ga
A generalized model of receptor function is proposed that relies on the essential
assumptions of the minimal two-state receptor theory (i.e., ligand binding
followed by receptor activation), but uses a different parametrization and allows
nonlinear response (transduction) for possible signal amplification. For the most
general case, three parameters are used: K(d), the classic equilibrium
dissociation constant to characterize binding affinity; ?, an intrinsic efficacy
to characterize the ability of the bound ligand to activate the receptor (ranging
from 0 for an antagonist to 1 for a full agonist); and ?, a gain (amplification)
parameter to characterize the nonlinearity of postactivation signal transduction
(ranging from 1 for no amplification to infinity). The obtained equation,
E/Emax=??L??+1-?L+Kd, resembles that of the operational (Black and Leff) or
minimal two-state (del Castillo-Katz) models, E/Emax=?L?+1L+Kd, with ?? playing a
role somewhat similar to that of the ? efficacy parameter of those models, but
has several advantages. Its parameters are more intuitive as they are
conceptually clearly related to the different steps of binding, activation, and
signal transduction (amplification), and they are also better suited for
optimization by nonlinear regression. It allows fitting of complex data where
receptor binding and response are measured separately and the fractional
occupancy and response are mismatched. Unlike the previous models, it is a true
generalized model as simplified forms can be reproduced with special cases of its
parameters. Such simplified forms can be used on their own to characterize
partial agonism, competing partial and full agonists, or signal amplification.