agonists and antagonists

9
Agonists and Antagonists APC T cell agonist peptide APC T cell antagonist peptide agonist peptide stimulation stimulation suppressed

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APC. antagonist peptide. agonist peptide. T cell. stimulation suppressed. stimulation. Agonists and Antagonists. APC. agonist peptide. T cell. +ve. -ve. Minimal Model. 3 species model:. [X]+[Z]=M=const. Irreversibility Branching Feedback with distinct time scale. - PowerPoint PPT Presentation

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Page 1: Agonists and Antagonists

Agonists and Antagonists

APC

T cell

agonistpeptide

APC

T cell

antagonist peptide

agonistpeptide

stimulation stimulationsuppressed

Page 2: Agonists and Antagonists

+ve

-ve

Minimal Model

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

• Irreversibility• Branching• Feedback with distinct time scale

3 species model:

Z → Lck

X → LckP

Y → Ag

k3 ∞ [Ant]

Minimal Model for cell signaling with positive and negative feedbacks

[X]+[Z]=M=const

Page 3: Agonists and Antagonists

+ve

-ve

Minimal Model

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

• Irreversibility• Branching• Feedback with distinct time scale

3 species model:

Z → Lck

X → LckP

Y → Ag

k3 ∞ [Ant]

Minimal Model for cell signaling with positive and negative feedbacks

[X]+[Z]=M=const €

dNx

dt= k2NxNyNz + k1NzNy

dNz

dt= −k2NxNyNz − k1NzNy

dNy

dt= −k3Ny

Mean field Analysis

Nx = 0, Ny = N, Nz = Minitial values (t=0) :

Rate equations :

Nz(t) + Nx (t) = const.number conservation :

Page 4: Agonists and Antagonists

+ve

-ve

Minimal Model

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

• Irreversibility• Branching• Feedback with distinct time scale

3 species model:

Z → Lck

X → LckP

Y → Ag

k3 ∞ [Ant]

Minimal Model for cell signaling with positive and negative feedbacks

[X]+[Z]=M=const

Nx (t) =k1M(F(t) −1)

Mk2 + k1F(t)

t →∞ ⏐ → ⏐ ⏐ k1M[N(Mk1 + k2) /k3 −1]

Mk2 + k1N(Mk1 + k2) /k3

= Mf (Mk2 /k1,Nk1/k3)

Ny (t) = Ne−k3t

t →∞ ⏐ → ⏐ ⏐ 0

N z( t) = M − N x(t)

F(t) = exp(Mk2 + k1)N(1− e−k3t )

k3

⎣ ⎢

⎦ ⎥

stability: no un-stable mode

Mean field Analysis

Solutions:

Page 5: Agonists and Antagonists

+ve

-ve

Minimal Model

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

• Irreversibility• Branching• Feedback with distinct time scale

3 species model:

Z → Lck

X → LckP

Y → Ag

k3 ∞ [Ant]

Minimal Model for cell signaling with positive and negative feedbacks

[X]+[Z]=M=const

Mean field Analysis

Page 6: Agonists and Antagonists

Effects of Stochastic Fluctuations

∂P(nx,ny,nz, t)

∂t= [k1ny (nz +1) + k2(nx −1)ny (nz +1)]P(nx −1,ny,nz +1, t) + k3(ny +1)P(nx,ny +1,nz, t)

− (k1nynz + k2nxnynz + k3ny )P(nx,ny,nz, t)

Master Equation:

Exactly Solvable

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

3 species model:

G(s1,s2 ,s3 ,t) = s1nx s2

ny s3nz

nz =0

M

∑ny =0

N

∑nx =0

M

∑ P(nx ,ny ,nz ,t)Generating function:

P(nx ,ny ,nz ,t) = δnx + nz, M λrr =nz

M

∑ pnzrNCny

k3

Ar + k3

1− exp(−(Ar + k3 )t( ) ⎡

⎣ ⎢

⎦ ⎥

N −ny

exp −ny(Ar + k3 )t( )

Ar = r((M − r )k2 + k1)

pnzr= rCnz

(−1)nzΓ(M + k1 / k2 +1− r )Γ(M + k1 / k2 − nz )

Γ(M + k1 / k2 +1− nz − r )Γ(M + k1 / k2 )

λr pnrr =n

M

∑ = 0 for n < M

= 1 for n = M

Solution:

Page 7: Agonists and Antagonists

Effects of Stochastic Fluctuations

∂P(nx,ny,nz, t)

∂t= [k1ny (nz +1) + k2(nx −1)ny (nz +1)]P(nx −1,ny,nz +1, t) + k3(ny +1)P(nx,ny +1,nz, t)

− (k1nynz + k2nxnynz + k3ny )P(nx,ny,nz, t)

Master Equation:

Exactly Solvable

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

3 species model:

G(s1,s2 ,s3 ,t) = s1nx s2

ny s3nz

nz =0

M

∑ny =0

N

∑nx =0

M

∑ P(nx ,ny ,nz ,t)

P(nx ,ny ,nz ,t) = δnx + nz, M λrr =nz

M

∑ pnzrNCny

k3

Ar + k3

1− exp(−(Ar + k3 )t( ) ⎡

⎣ ⎢

⎦ ⎥

N −ny

exp −ny(Ar + k3 )t( )

Ar = r((M − r )k2 + k1)

pnzr= rCnz

(−1)nzΓ(M + k1 / k2 +1− r )Γ(M + k1 / k2 − nz )

Γ(M + k1 / k2 +1− nz − r )Γ(M + k1 / k2 )

λr pnrr =n

M

∑ = 0 for n < M

= 1 for n = M

Generating function:

Solution:

[X]+[Z]=M=const

small Nsmall k3

Fixed k3/N

Stochastic Analysis

Mean field

large Nlarge k3

Fixed k3/N

purely stochastic origin of bimodality

Page 8: Agonists and Antagonists

Effects of Stochastic Fluctuations

∂P(nx,ny,nz, t)

∂t= [k1ny (nz +1) + k2(nx −1)ny (nz +1)]P(nx −1,ny,nz +1, t) + k3(ny +1)P(nx,ny +1,nz, t)

− (k1nynz + k2nxnynz + k3ny )P(nx,ny,nz, t)

Master Equation:

Exactly Solvable

Y + Z k1 ⏐ → ⏐ X + Y

Z + Y + X k2 ⏐ → ⏐ 2X + Y

Y k3 ⏐ → ⏐ ∅

3 species model:

G(s1,s2 ,s3 ,t) = s1nx s2

ny s3nz

nz =0

M

∑ny =0

N

∑nx =0

M

∑ P(nx ,ny ,nz ,t)

P(nx ,ny ,nz ,t) = δnx + nz, M λrr =nz

M

∑ pnzrNCny

k3

Ar + k3

1− exp(−(Ar + k3 )t( ) ⎡

⎣ ⎢

⎦ ⎥

N −ny

exp −ny(Ar + k3 )t( )

Ar = r((M − r )k2 + k1)

pnzr= rCnz

(−1)nzΓ(M + k1 / k2 +1− r )Γ(M + k1 / k2 − nz )

Γ(M + k1 / k2 +1− nz − r )Γ(M + k1 / k2 )

λr pnrr =n

M

∑ = 0 for n < M

= 1 for n = M

Generating function:

Solution:

[X]+[Z]=M=const

Origin of Stochastic Bistability

Z

X

rate 2

rate 1

Zd ~ 1/(k3ny)

f ~ 1/(k2nxnynz)

fd

P()

(activation)

(de-activation)

Page 9: Agonists and Antagonists

Cell Decision Mediated by Stochastic Fluctuations

agonistantagonist

Signaling product

No signal

M. Artyomov, JD, M. Kardar, A. Chakraborty PNAS (2007)