TY - JOUR
T1 - The mammalian MAPK/ERK pathway exhibits properties of a negative feedback amplifier
AU - Sturm, Oliver E.
AU - Orton, Richard
AU - Grindlay, Joan
AU - Birtwistle, Marc
AU - Vyshemirsky, Vladislav
AU - Gilbert, David
AU - Calder, Muffy
AU - Pitt, Andrew
AU - Kholodenko, Boris
AU - Kolch, Walter
PY - 2010/12/21
Y1 - 2010/12/21
N2 - Three-tiered kinase modules, such as the Raf-MEK (mitogen-activated or extracellular signal-regulated protein kinase kinase)-ERK (extracellular signal-regulated kinase) mitogen-activated protein kinase pathway, are widespread in biology, suggesting that this structure conveys evolutionarily advantageous properties. We show that the three-tiered kinase amplifier module combined with negative feedback recapitulates the design principles of a negative feedback amplifier (NFA), which is used in electronic circuits to confer robustness, output stabilization, and linearization of nonlinear signal amplification. We used mathematical modeling and experimental validation to demonstrate that the ERK pathway has properties of an NFA that (i) converts intrinsic switch-like activation kinetics into graded linear responses, (ii) conveys robustness to changes in rates of reactions within the NFA module, and (iii) stabilizes outputs in response to drug-induced perturbations of the amplifier. These properties determine biological behavior, including activation kinetics and the response to drugs.
AB - Three-tiered kinase modules, such as the Raf-MEK (mitogen-activated or extracellular signal-regulated protein kinase kinase)-ERK (extracellular signal-regulated kinase) mitogen-activated protein kinase pathway, are widespread in biology, suggesting that this structure conveys evolutionarily advantageous properties. We show that the three-tiered kinase amplifier module combined with negative feedback recapitulates the design principles of a negative feedback amplifier (NFA), which is used in electronic circuits to confer robustness, output stabilization, and linearization of nonlinear signal amplification. We used mathematical modeling and experimental validation to demonstrate that the ERK pathway has properties of an NFA that (i) converts intrinsic switch-like activation kinetics into graded linear responses, (ii) conveys robustness to changes in rates of reactions within the NFA module, and (iii) stabilizes outputs in response to drug-induced perturbations of the amplifier. These properties determine biological behavior, including activation kinetics and the response to drugs.
UR - http://www.scopus.com/inward/record.url?scp=78650635354&partnerID=8YFLogxK
U2 - 10.1126/scisignal.2001212
DO - 10.1126/scisignal.2001212
M3 - Article
C2 - 21177493
AN - SCOPUS:78650635354
SN - 1945-0877
VL - 3
SP - 1
EP - 7
JO - Science Signaling
JF - Science Signaling
IS - 153
M1 - ra90
ER -