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Towards More Realistic Affinity Maturation Modeling Erich R. Schmidt, Steven H. Kleinstein Department of Computer Science, Princeton University July 19,

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Presentation on theme: "Towards More Realistic Affinity Maturation Modeling Erich R. Schmidt, Steven H. Kleinstein Department of Computer Science, Princeton University July 19,"— Presentation transcript:

1 Towards More Realistic Affinity Maturation Modeling Erich R. Schmidt, Steven H. Kleinstein Department of Computer Science, Princeton University July 19, 2001

2 Germinal center models Recent germinal center models: simple responses (haptens – Ox, NP) single affinity- increasing mutation simple B cell model no inter-cellular signals no internal dynamics Address limitations: more complex receptor affinity space multiple affinity- increasing mutations more realistic model of B cell inter-cellular signals signal memory

3 Simulation B cell receptor affinity B cell Germinal center More complex, realistic Specific: Ox, NP Discrete/ stochastic simulation affinity landscape internal dynamics population dynamics

4 Affinity landscapes: NK landscape model N: sequence length  receptor space size K: internal interactions  landscape ruggedness NK : easy to model different antigen, check stats vs. experimental data K=0K=mediumK=highOx,NP

5 NK parameter values proposed by Kauffman/Weinberger: correctly predicts: number of steps to local optima fraction of higher-affinity neighbors “conserved” sites in local optima

6 Individual mutations vs. population dynamics Kauffman/Weinberger: single cell walk mutations: uphill no time no other events Our simulation: entire population dynamics mutations: random time-dependent division, death

7 Simulation B cell receptor affinity B cell Germinal center More complex, realistic Specific: phOx, NP Discrete/ stochastic simulation

8 B cell model – decision making network input node (receptor affinity) mutationdeathdivision output nodes (rates) functional nodes fitness function (division)

9 Germinal center model single seed all cells share same parameters dynamic, stochastic, discrete simulate for 14 days different steps: change network parameters search: best network for affinity maturation

10 Expectations Previous work: Ox, NP single affinity-increasing mutation fitness function = threshold NK landscape rugged, multiple peaks expected smaller slope Ox,NPNK

11 Results threshold select for small percentage of affinity- increasing mutations high-affinity seed

12 Results low affinity seed smaller slope very hard to walk up: smaller slope doesn’t help overall affinity maturation

13 Conclusions dynamic model on NK landscape generates affinity maturation not reaching local optima best division rate is a threshold function affinity of seeding cell important factor total mutation count consistent with bio data Kauffman: all mutations up our simulation: random mutations (up+down)

14 Future work more complex decision network optimization problem: mutate network, not only parameters B cell receptor affinity B cell Germinal center More complex, realistic Specific: phOx, NP Discrete/ stochastic simulation More realistic

15 Acknowledgements Steven Kleinstein, Jaswinder Pal Singh Martin Weigert Stuart A. Kauffman, Edward D. Weinberger, Bennett Levitan (Santa Fe)

16 The End


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