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How cells make decisions?. outputs. External signal s. Information Processing System. The cell is a (bio)chemical computer. Hanahan & Weinberg (2000). ?. ?. Smad. p21. MKK. MAPK. MAPK-P. PP. Signal transduction networks. Hanahan & Weinberg (2000). d [ protein ] dt.
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outputs External signals Information Processing System The cell is a (bio)chemical computer Hanahan & Weinberg (2000)
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Smad p21 MKK MAPK MAPK-P PP Signal transduction networks Hanahan & Weinberg (2000)
d [protein] dt = synthesis - degradation ‘Birth control’ for proteins DNA transcription factor transciption RNA translation protein
synthesis degradation degradation S linear 3 rate (dR/dt) k1 2 k2 R S=1 response (R) synthesis R signal (S) Gene expression S = mRNA R = protein Signal-response curve
Michaelis-Menten enzyme kinetics since [Eo] = [E] + [ES]
S 2 ADP ATP 1.5 dephospho- rylation rate (dRP/dt) k1 1 R RP k2 phospho- rylation 0.5 H2O Pi 0.25 RP sigmoidal R 0 1 response (RP) dephosphorylation phosphorylation signal (S) Protein phosphorylation Signal-response curve ‘Buzzer’ graded and reversible zero order ultrasensitivity Goldbeter & Koshland, 1981
k p k p R RP RP2RPn …… for n=2 Multiple phosphorylation where K=k/p
n=3 RP3 R K=k/p n=4 Hill equation: RP4 R K=k/p K=k/p Multiple phosphorylation n=2 RP2 R K=k/p
k3 synthesis k4 X S 3 degradation k1 k2 R rate (dR/dt) 2 1 R adapted S R X Response is independent of Signal time Two linear modules Perfect adaptation
S + X - + R Feed-forward loop S + X + - R R increases for S increase R decreases for S decrease R decreases for S increase R increases for S decrease
X S + RA S XA RA R + XA Feed-forward loop with two buzzers Cock and fire
Another way to get perfect adaptation S k1 k3 k0 R’ R k2
Bacterial chemotaxis swimming (counter-clockwise) tumbling (clockwise) The same principle, different deployment S k0 k1 R’ R k3 k2
16 8 S 0 rate (dR/dt) open k1 k2 R k0 synthesis degradation k3 EP E closed k4 R mutual activation response (R) response (R) ‘Toggle’ switch Scrit1 Scrit2 signal (S) signal (S) Linear module & buzzer Protein synthesis: positive feedback bistability ‘Fuse’
Example: Fuse dying response (R) living signal (S) Apoptosis (Programmed Cell Death)
S k1 k2 R k0 k3 EP E k4 The lac operon (‘toggle’ switch) S (extracellular lactose) EP R (intracellular lactose)
Multistability in the lactose utilization network of Escherichia coli ERTUGRUL M. OZBUDAK1,*, MUKUND THATTAI1,*, HAN N. LIM1, BORIS I. SHRAIMAN2 & ALEXANDER VAN OUDENAARDEN1 Initially uninduced cells grown for 20 hrs in 18 M TMG Initially uninduced cells (lower panel) andinduced cells (upper panel)grown in media containing different concentration of TMG TMG = thio-methylgalactoside
‘Death control’ for proteins d [protein] dt = synthesis - degradation proteasome ubiquitilation system degraded protein
S k1 k2 R k0 k2' degradation k4 EP E 1.8 k3 rate (dR/dt) 1.2 synthesis mutual inhibition 0.6 response (R) R signal (S) Linear module & buzzer Protein degradation: mutual inhibition
Oscillators: three modules
Scrit1 Scrit2 k5 k6 response (R) X S k2' k1 R k2 k0 PhasePlane k3 EP E k4 signal (S) R X Positive and negative feedback oscillations (activator-inhibitor)
p53 Mdm2 p53-CFP and Mdm2-YFP levelsin the nucleus after -irradiation Period of oscillation: 440 100 min
S k0' k2 X R k1 k0 k3 Scrit2 Scrit1 EP E k4 response (R) R signal (S) X Positive and negative feedback oscillations (substrate depletion)
S k1 k2 X k0 k2' k3 (2) Scrit1 Scrit2 Y YP k4 response (RP) k5 YP RP R X k6 (1) RP signal (S) time Negative feedback and oscillation
production removal 1.5 1 rate (dR/dt) 0.5 homeostatic response (R) R signal (S) Negative feedback and homeostasis S k0 R k2 k4 EP E k3
Typical biosynthetic pathway aminoacid demand protein