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Modeling, visualizing, and annotating immunoreceptor signaling systems Lily Chylek Cornell University & Los Alamos National Laboratory.

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Presentation on theme: "Modeling, visualizing, and annotating immunoreceptor signaling systems Lily Chylek Cornell University & Los Alamos National Laboratory."— Presentation transcript:

1 Modeling, visualizing, and annotating immunoreceptor signaling systems Lily Chylek Cornell University & Los Alamos National Laboratory

2 Outline Methods for model visualization Extended contact map and model guide Applications: large-scale models of immunoreceptor signaling

3 Signaling proteins Multiple components mediate interactions with other proteins. Interactions regulated by post-translational modifications at multiple sites. Combinatorial complexity: many possible binding and modification states. ZAP-70

4 Features of early events in immunoreceptor signaling Multi-subunit receptors (e.g., Fc ε RI, TCR) interact with ligands Phosphorylation of tyrosine residues in ITAM motifs Binding of SH2 domains to receptor Regulation of kinases by phosphorylation of specific residues Rule-based modeling offers a viable approach to modeling these (and other) cell signaling systems.

5 Rule-based modeling Prospects: A great deal of information is available about a number of signal transduction systems. This information can be used to specify rules. Algorithms and software tools are available that allow us to simulate large-scale rule-based models. Challenges: How can we communicate the content of a large model? Can we associate each rule with its biological basis?

6 Rule-based modeling Prospects: A great deal of information is available about a number of signal transduction systems. This information can be used to specify rules. Algorithms and software tools are available that allow us to simulate large-scale rule-based models. Challenges: How can we communicate the content of a large model? Can we associate each rule with its biological basis? Rec(a) + Lig(l,l) Rec(a!1).Lig(l!1,l) kp1, km1Rec(a) + Lig(l,l!1) Rec(a!2).Lig(l!2,l!1) kp2,km2 Rec(b ∼ Y) + Lyn(U,SH2) Rec(b ∼ Y!1).Lyn(U!1,SH2) kpL, kmL Lig(l!1,l!2).Lyn(U!3,SH2).Rec(a!2,b Y!3).Rec(a!1,b ∼ Y) -> Lig(l!1,l!2).Lyn(U!3,SH2).Rec(a!2,b Y!3).Rec(a!1,b ∼ pY) pLb Lig(l!1,l!2).Lyn(U,SH2!3).Rec(a!2,b pY!3).Rec(a!1,b ∼ Y) -> Lig(l!1,l!2).Lyn(U,SH2!3).Rec(a!2,b pY!3).Rec(a!1,b ∼ pY) pLbs Lig(l!1,l!2).Lyn(U!3,SH2).Rec(a!2,b Y!3).Rec(a!1,g ∼ Y) -> Lig(l!1,l!2).Lyn(U!3,SH2).Rec(a!2,b Y!3).Rec(a!1,g ∼ pY) pLg Lig(l!1,l!2).Lyn(U,SH2!3).Rec(a!2,b pY!3).Rec(a!1,g ∼ Y) -> Lig(l!1,l!2).Lyn(U,SH2!3).Rec(a!2,b pY!3).Rec(a!1,g ∼ pY) pLgs Rec(b ∼ pY) + Lyn(U,SH2) Rec(b ∼ pY!1).Lyn(U,SH2!1) kpLs, kmLsRec(g ∼ pY) + Syk(tSH2) Rec(g ∼ pY!1).Syk(tSH2!1) kpS, kmS Lig(l!1,l!2).Lyn(U!3,SH2).Rec(a!2,b ∼ Y!3).Rec(a!1,g pY!4).Syk(tSH2!4,l ∼ Y) -> Lig(l!1,l!2).Lyn(U!3,SH2).Rec(a!2,b ∼ Y!3).Rec(a!1,g pY!4).Syk(tSH2!4,l ∼ pY) pLS

7 Method 1: Individual rules How are components transformed by a rule? Advantage Rules are easily visualized. Problem Locally comprehensible, globally incomprehensible.

8 Method 2: Contact map How do molecules bind? Advantages All molecules, components, states, and binding interactions are presented. Can be generated automatically (GetBonNie, RuleBender, Rulebase/Kappa). Problems Lacks clear representation of enzyme-substrate relationships. Does not always show accurate substructure.

9 Method 3: Molecular interaction map How do molecules interact, and how do interactions affect each other? Advantage Catalytic interactions are distinguishable from binding interactions. Each molecule is shown only once. Problem Too much information (context). Maps become cluttered for complex networks.

10 What do we need from a diagram? A comprehensive representation of molecules and interactions in a model. Understandable, not overloaded with information. Connections to rules and biological knowledge.

11 Outline Methods for model visualization Extended contact map and model guide Applications: large-scale models of immunoreceptor signaling

12 Extended contact map What is the big picture of molecules and interactions in a model?

13 Extended contact map Multiple levels of nesting to show protein substructure.

14 Extended contact map Multiple levels of nesting to show protein substructure. Distinguish different types of interactions (binding vs. catalysis).

15 Extended contact map Multiple levels of nesting to show protein substructure. Distinguish different types of interactions (binding vs. catalysis).

16 Extended contact map Multiple levels of nesting to show protein substructure. Distinguish different types of interactions (binding vs. catalysis). Show sites of post- translational modification.

17 Extended contact map Use tags to show locations of molecules.

18 Extended contact map Use tags to show locations of molecules. Use shading to indicate hierarchy of molecules in signaling.

19 Extended contact map Use tags to show locations of molecules. Use shading to indicate hierarchy of molecules in signaling. Connect interactions to rules, where context is accounted for.

20 Extended contact map Use tags to show locations of molecules. Use shading to indicate hierarchy of molecules in signaling. Connect interaction to rule(s), where context is accounted for.

21 Annotation: Model guide 88

22 Can we model and visualize other common processes in cell signaling?

23 Ubiquitination cascade E1 catalyzes transfer of ubiquitin from itself to E2. E3 catalyzes transfer of ubiquitin from E2 to target protein.

24 HRas HRas is a GTPase.

25 HRas HRas is a GTPase, stimulated by RasGAP.

26 HRas HRas is a GTPase, stimulated by RasGAP. Nucleotide exchange stimulated by Sos1.

27 HRas HRas is a GTPase, stimulated by RasGAP. Nucleotide exchange stimulated by Sos1. Sos1 allosterically activated by binding HRas.

28 HRas HRas is a GTPase, stimulated by RasGAP. Nucleotide exchange stimulated by Sos1. Sos1 allosterically activated by binding HRas. Raf-1 binds GTP- bound HRas.

29 Outline Methods for model visualization Extended contact map and model guide Applications: large-scale models of immunoreceptor signaling

30 Conclusions As we formulate larger models, it will be necessary to have a consistent means of model visualization and annotation. An extended contact map and model guide annotate a signal-transduction system in a form that is both visual and executable. http://bionetgen.org/index.php/Extended_Contact_Maps

31 Thanks! Bill Hlavacek Bin Hu Michael Blinov Thierry Emonet Jim Faeder Byron Goldstein Ryan Gutenkunst Jason Haugh Tomasz Lipniacki Richard Posner Jin Yang

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