Multiscale Modeling in Biology

Speaker: 

Professor Mark Alber

Institution: 

University of Notre Dame

Time: 

Friday, November 14, 2008 - 2:00pm

Location: 

RH 440R

Multiscale modeling approach typical of systems biology tends to mix continuous, discrete, \
deterministic, and probabilistic submodels. To prevent the loss of blood following a break \
in blood vessels, components in blood and the vessel wall interact rapidly to form a clot t\
o limit hemorrhage. In this talk we will describe a multiscale hybrid model of thrombus for\
mation consisting of components for modeling viscous, incompressible blood plasma; coagulat\
ion pathway; quiescent and activated platelets; blood cells; activating chemicals; fibrinog\
en; the vessel walls and their interactions. At macro scale blood flow is described by the \
incompressible Navier-Stokes equations and is numerically solved using the projection metho\
d. At micro scale, cell movement, cell-cell adhesion, cell-flow and cell-vessel wall intera\
ctions are described through an extended stochastic discrete Cellular Potts Model (CPM). Si\
mulation results show development of an inhomogeneous internal structure of the clot confir\
med by the preliminary experimental data. It is also demonstrated that dependence of the cl\
ot size on the blood flow rate in simulations is close to the one observed experimentally.

In the second half of the talk a continuous limit will be discussed of a two-dimensional st\
ochastic CPM describing cells moving in a medium and reacting to each other through direct \
contact, cell-cell adhesion, and long range chemotaxis. Contrary to classical Keller-Segel \
model, solutions of the obtained equation do not collapse in finite time and can be used ev\
en when relative volume occupied by cells is quite large. A very good agreement was demonst\
rated between CPM Monte Carlo simulations and numerical solutions of the obtained macroscop\
ic nonlinear diffusion equation. Combination of microscopic and macroscopic models was used\
to simulate growth of structures similar to early vascular networks.

Xu, Z., Chen, N., Kamocka, M.M., Rosen, E.D., and M.S. Alber [2008], Multiscale Model of Th\
rombus Development, Journal of the Royal Society Interface 5 705-722.

Alber, M., Chen, N., Lushnikov, P., and S. Newman [2007], Continuous macroscopic limit of a\
discrete stochastic model for interaction of living cells, Physical Review Letters 99 1681\
02.

Lushnikov, P.P., Chen, N., and M.S. Alber, Macroscopic dynamics of biological cells interac\
ting via chemotaxis and direct contact, Physical Review E (to appear).

What is different about the ergodic theory of stochastic PDEs (vs ODEs)

Speaker: 

Professor Jonathan Mattingly

Institution: 

Duke University

Time: 

Friday, November 14, 2008 - 4:00pm

Location: 

RH 306

I will discuss the difficulties which arise when one considers the
long time behavior of a stochastically forced PDE. I will try to
highlight that there are different cases which require very different
ideas. Some cases can be seen as extensions of what is done in finite
dimensions, others require new tools and ideas. I will concentrate on
the case of degenerately forced SPDEs. I will describe an extension of
Hormander's "sum of squares theorem" to hypo-elliptic operators in
infinite dimensions. I will discuss the concert examples of the 2D
Navier Stokes equations on the torus and sphere as well as a class of
reaction diffusion equations. In these contexts the discussion will
center on the transfer of randomness between scales.

The Topology of DNA-Protein Interactions

Speaker: 

Dr. Dorothy Buck

Institution: 

Applied Mathematics, Imperial College London

Time: 

Monday, December 1, 2008 - 4:00pm

Location: 

RH 306

he central axis of the famous DNA double helix is
often topologically constrained or even circular.
The topology of this axis can influence which
proteins interact with the underlying DNA. Subsequently, in all cells there are
proteins whose primary function is to change the DNA axis
topology -- for example converting a torus link into an unknot.
Additionally, there are several protein families that change the axis
topology as a by-product of their interaction with DNA.

This talk will describe typical DNA conformations, and the families of
proteins that change these conformations. I'll present a few examples
illustrating how 3-manifold topology has been useful in understanding certain
DNA-protein interactions, and discuss the most common topological techniques
used to attack these problems.

Phase-filed models for multiphase complex fluids: modeling, numerical analysis and simulations

Speaker: 

Professor Jie Shen

Institution: 

Purdue University

Time: 

Monday, March 30, 2009 - 4:00pm

Location: 

RH 306

I shall present an energetic variational phase field model for
multiphase incompressible flows which leads to a set of coupled
nonlinear system consisting a phase equation and the Navier-Stokes
equations. We shall pay particular attention to situations with large
density ratios as they lead to formidable challenges in both analysis
and simulation.

I shall present efficient and accurate numerical schemes for solving
this coupled nonlinear system, and show ample numerical results (air
bubble rising in water, Newtonian bubble rising in a polymeric fluid, defect
motion in a liquid crystal flow, etc.) which not only demonstrate the
effectiveness of the numerical schemes, but also validate the
flexibility and robustness of the phase-field model.

Reflectionless measures

Speaker: 

Christian Remling

Institution: 

University of Oklahoma

Time: 

Thursday, November 13, 2008 - 2:00pm

Location: 

RH 306

Reflectionless measures are interesting objects because
they arise as limiting measures of spectral measures of arbitrary
Schr"odinger operators with some absolutely continuous spectrum.
In this talk, I'd like to review the definition and some background
material and then discuss more recent work, joint with Alexei Poltoratski,
on reflectionless measures.

Pisot tilings of the line and the discrete spectrum conjecture

Speaker: 

Professor Robert Williams

Institution: 

UT Austin

Time: 

Tuesday, November 18, 2008 - 3:00pm

Location: 

RH 440 R

I will present some of the results by Marcy Barge and Jaroslaw Kwapisz (based on their paper "Geometric Theory of unimidular Pisot substitutions", Amer. J. Math., vol. 128 (2006), no. 5, pp. 1219--1282).

There are two classical ways of studying substitution tilings of the line: symbolic dynamics, and endomorphisms of ``train tracks". The authors give a strikingly new geometric approach and in particular show that if the tiling has a unimodular Pisot matrix of dimension d, then there is a factor onto the d-dimensional torus. In fact, they have a preprint removing the unimodular assumption. I propose to begin defining tilings and the tiling space X of a tiling T. X is a compact metric space that contains all tilings which have the same local patterns as T. In dimension 1 (the subject of this talk) X is similar to a solenoid.

I will not assume any familiarity with tiling theory.

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