[Todos] PROXIMOS SEMINARIOS
Fernando V. Molina
fmolina en qi.fcen.uba.ar
Jue Jul 24 13:33:08 ART 2008
Lunes 28 de julio de 2008 - 13 hs
Aula de Seminarios del INQUIMAE, 3er piso Pab. II
Prof. Igal Szleifer
Department of Biomedical Engineering
Northwestern University
Ligand-receptor binding in confined environments: from specific
protein adsorption to nanoparticle attachment
Abstract:
Ligand-receptor binding is a ubiquitous process in biology and it has
been the basis for the design of biosensors and drug delivery
systems. The question that we address in this presentation is what is
the best way to optimize binding when the ligands and receptors are
in a confined environment. This important practical question is one
example of the more general problem of the effect of confinement in
chemical equilibrium reactions. To understand this question we will
present predictions form a molecular theoretical approach that
enables us to understand the relationship between molecular
organization, packing and ligand-receptor binding. Explicit
comparisons with experimental observations will be shown where the
predictions of the theory are in very good agreement with
experimental observations. We will discuss three different scenarios.
The first is when both ligand and receptor are attached to surfaces,
in the presence of polymer spacers. This case is relevant for cell
binding and in the case of interactions between liposomes and cell
membranes. The second problem relates to the way in which the binding
of proteins to surfaces and nanoparticles can be optimized using
polymer molecules as spacers. The last case involves the binding of
polymer-coated nanoparticles to surfaces. In these systems we discuss
the role that surface mobility of the ligands has on the binding and
how this effect can be used to optimize targeted drug delivery. The
results of the theory will be summarized in terms of how to design
surface coatings for surfaces and nanoparticles that optimize binding
by the proper understanding of the coupling between molecular
interactions, confinement and the flexibility of polymer molecules.
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