29th January 2015, 17h. Anfiteatro A IBMC,
Rua do Campo Alegre 823, Porto
Abstract
Many
processes in cell and molecular biology can be
described by biochemical reaction networks. It
is useful to study these networks using
computer simulations because they allow us to
quantitatively investigate hypotheses about
the networks. Deterministic simulations are sufficient to predict average
behaviors at the population level, but they
cannot address questions about noise, random
switching between stable states of the system,
or the behaviors of systems with very few
molecules of key species. These topics are
investigated with stochastic simulations.
In this first
Bridges talk, we will review, in an intuitive,
and hopeffuly comprehensive manner,
some key Stochastic Simulation Algorithms used
in Sistems Biology. We will give several illustrations of
these methods [pdf
presentation]
Date/Venue
12th March 2015, 17h.
Anfiteatro 0.31 Dep Matemática FCUP
Rua do Campo Alegre, 687, Porto
Title
Mechanics
of the contractile ring during cytokinesis
Brief background and aims
of our lab:
We have been exploring the power of
quantitative live imaging assays to study
cytokinesis in the early C. elegans embryo.
Cytokinesis
requires the assembly and constriction of a
contractile ring at the equator of the mother
cell. The contractile ring is an acto-myosin
filamentous structure which constricts while
bringing behind it the plasma membrane,
generating a physical barrier between the two
daughter cells. The ring is thought to
constrict via the action of myosin motor
activity that slides actin filaments past one
another and actin filament depolymerization.
The whole process of assembly and constriction
of the ring takes 6 minutes in our system. Due
to the contractile ring highly transient and
dynamic nature, the understanding of its
mechanics is challenging and yet poorly
understood.
Mathematical models exist but suffer from a
lack of quantitative in vivo data. They
generally use parameters from in vitro data
obtained from a mix of experimental setups/
molecules of different organisms. The aim of
our lab is to gather quantitative information
about the dynamic behavior of contractile ring
components, the roles of actin filament
dynamics, myosin II motility, and actin
regulators during contractile ring
constriction, as well as about the
ultra-structural organization of the
contractile ring. We expect that these
parameters, all derived from the same
experimental system, will allow us to
significantly improve our understanding of the
mechanics of the contractile ring as well as
develop computational models aimed at
recapitulating the process of contractile ring
assembly and constriction. To generate new
models, whose predictions we will be able to
test in our highly tractable experimental
system, we are currently seeking to establish
collaborations with mathematicians and
biophysicists.
Topics I would like
to address in the seminar:
The seminar I propose to present would be
entitled "Mechanics of the contractile ring
during cytokinesis"
and would consist of the description of
results we have already obtained:
1) when we use a laser microsurgery assay to
probe how the constricting contractile ring
responds to discontinuities in its structure
2) when we follow constricting rings in the
presence of myosin mutants that have already
been characterized in vitro and are known to
slide actin filaments at different velocities.