MNIBS 2005-2009 Multiscale Modeling of Nanostructured Interfaces for Biological Sensors
NMP-NSF-1 EU-NSF Coordinated activities in computational materials research
The kinetics of protein adsorption are studied using a generalized diffusion approach which shows that the time-determining step in the adsorption is the crossing of the kinetic barrier presented by the polymers and already adsorbed proteins. The potential of mean-force between the adsorbing protein and the polymer-protein surface changes as a function of time due to the deformation of the polymer layers as the proteins adsorb. Furthermore, the range and strength of the repulsive interaction felt by the approaching proteins increases with grafted polymer molecular weight and surface coverage. The effect of molecular weight on the kinetics is very complex and different than its role on the equilibrium adsorption isotherms. The very large kinetic barriers make the timescale for the adsorption process very long and the computational effort increases with time, thus, an approximate kinetic approach is developed. The kinetic theory is based on the knowledge that the time-determining step is crossing the potential-of-mean- force barrier. Kinetic equations for two states ( adsorbed and bulk) are written where the kinetic coefficients are the product of the Boltzmann factor for the free energy of adsorption (desorption) multiplied by a preexponential factor determined from a Kramers-like theory. The predictions from the kinetic approach are in excellent quantitative agreement with the full diffusion equation solutions demonstrating that the two most important physical processes are the crossing of the barrier and the changes in the barrier with time due to the deformation of the polymer layer as the proteins adsorb/desorb. The kinetic coefficients can be calculated a priori allowing for systematic calculations over very long timescales. It is found that, in many cases where the equilibrium adsorption shows a finite value, the kinetics of the process is so slow that the experimental system will show no adsorption. This effect is particularly important at high grafted polymer surface coverage. The construction of guidelines for molecular weight/surface coverage necessary for kinetic prevention of protein adsorption in a desired timescale is shown. The time-dependent desorption is also studied by modeling how adsorbed proteins leave the surface when in contact with a pure water solution. It is found that the kinetics of desorption are very slow and depend in a nonmonotonic way in the polymer chain length. When the polymer layer thickness is shorter than the size of the protein, increasing polymer chain length, at fixed surface coverage, makes the desorption process faster. For polymer layers with thickness larger than the protein size, increases in molecular weight results in a longer time for desorption. This is due to the grafted polymers trapping the adsorbed proteins and slowing down the desorption process. These results offer a possible explanation to some experimental data on adsorption. Limitations and extension of the developed approaches for practical applications are discussed. [hide]
Scientific Board
Manuel Laso (PI)
Universidad Politecnica Madrid, Spain ►
Juan J. de Pablo
University of Madison, United States ►
Orlando Guzman
Universidad Autonoma Metropolitana, Mexico ►
Martin Kroger
ETH Zurich, Germany/Switzerland ►
Monica Olvera de la Cruz
Northwestern University, United States ►
Hans-Christian Ottinger
ETH Zurich, Switzerland ►
Igal Szleifer
Purdue University, United States ►
Doros Theodorou
National Technical University of Athens, Greece ►
Scientific Stuff
Rodolfo Bermejo
Universidad Politecnica Madrid, Spain ►
David Catandeda
Universidad Autonoma Metropolitan, Mexico ►
Faith Coldren
Universidad Politecnica Madrid, Spain ►
Katerina Foteinopoulou
Universidad Politecnica Madrid, Spain ►
Brian Gettelfinger
University of Madison, United States ►
Francisco Hung
University of Madison, United States ►
Patrick Ilg
ETH Zurich, Switzerland ►
Nieves Jimeno
Universidad Politecnica Madrid, Spain ►
Nikos Karayiannis
Universidad Politecnica Madrid, Spain ►
Adrien Leygue
National Technical University of Athens, Greece ►
Sharon Loverde
Northwestern University, United States ►
Grigoris Megariotis
National Technical University of Athens, Greece ►
Shihong Meng
Purdue University, United States ►
Juan Luis Prieto
Universidad Politecnica Madrid, Spain ►
Jose Velez
Universidad Autonoma Metropolitan, Mexico ►
Antonia Vyrkou
National Technical University of Athens, Greece ►
Multiscale Modeling of Nanostructured Interfaces for Biological Sensors
The unusual properties of liquid cyrstals have been known and very profitably exploited for more than half a century. Yet they still seem to keep useful surprises in store: the realization that liquid crystalline materials can be applied to detect the presence of peptides, proteins and toxins is very new. The first experiments on liquid crystal-based biosensors are only a few years old. Understanding how these sensors can, under favourable conditions, detect individual molecules is still a work in progress, which requires a combined, multi-level approach. The development of such a multi-level, hierachical modelling technique was the primary objective of MNIBS. In addition to its intrinsic scientific value, a thorough understanding of the mechanisms of the extreme sensitivity of liquid crystals to certain biological molecules would make it possible to design sensors tailored to specific proteins or viruses. The most striking, and most useful, feature of liquid crystals in the context of biosensors is their ability to "amplify" a signal at the molecular level. The arrival of a single protein molecule at the exposed surface of a liquid crystal has been observed to trigger a re-organization of the liquid crystal around the protein. This remarkable amplification effect that takes place in liquid crystal sensors is triggered by an event at the molecular level (a few nanometers) and spontaneously develops macroscopic size (a few milimeters). It is thus not surprising that the techniques used to model the ordering transtion of liquid crystal molecules around the protein cannot be applied to the spreading of ordering to macroscopic size. Conversely, those continuum models that are the most natural framework to describe macroscopic behaviour have no molecular resolution. There is thus no single, all-encompassing technique that can tackle the amplification problem MNIBS has addressed this apparent impasse by means of a hierarchical strategy, in which different techniques, each ideally suited to a particular length and time scale, are combined in a thermodynamically consistent way. MNIBS was jointly funded by the EC and the NSF. Contractors on the EC side were the Universidad Politecnica de Madrid (UPM), the National Technical University Athens (NTUA) and the Eidgenössische Technische Hochschule Zurich (ETH Zurich). A new contractor joined the Consortium on January 1st 2007: the Universidad Autonoma de Mexico, funded also by the EC under its call FP6-2006-TTC-TU-Priority-3. US contractors were the University of Wisconsin-Madison (UW), Northwestern University (NW) and Purdue University (PU). An outstanding success of MNIBS was the fruitful collaboration of groups from the EC, USA, and Mexico. Thanks to the joint character of the Call, EC and US groups received independent but coordinated financial support. A TTC project enabled the Mexican group to join the project after its first year. Given the variety of modelling techniques used in MNIBS, it was a prerequisite to include in the Consortium the leading experts in the fields, which not always reside in EC member countries. The joint Call scheme has proved to be a very flexible tool for enabling collaboration beyond the borders of the EC. All participants in MNIBS have contributed highly specialized expertise in areas as diverse as atomistic molecular modelling, mesoscopic, stochastic techniques, dynamic mean field and single-molecule theory, and continuum mechanics. Overall thermodynamic consistency was given high priority. A group specializing in non-equilibrium thermodynamics was charged with the task of guaranteeing that information transfer across the different spatial and temporal scales complied with thermodynamic consistency. In this respect, one of the most prominent successes of MINBS was the effective integration of all modelling techniques into a multiscale tool that went all the way from the molecular to the macroscopic level:The successful meshing of the three description levels into a practical simulation and design tool by means of a thermodynamically consistent formalism was a very satisfactory confirmation of the ideas advanced in the proposal phase. As a result of the convergence of all the modelling techniques developed or applied in MNIBS, a first principles simulation and design of LC-based, single-molecule sensors for proteins and toxins is now possible. Several of the techniques developed in the project represent the current state-of-the-art in the simulation of soft condensed matter at the micro-, meso-, and macroscopic levels. These advances are reflected in over 40 publications in top level journals, including several Physical Review Letters, Soft Matter, Journal of Physical Chemistry B, etc. MNIBS also made a significant contribution to dissemination and outreach through successful contacts with a number of industrial and academic partners. In view of the successful achievement of all objectives, and thanks to a contract extension granted by the EC, such dissemination activities were given greater priority than originally planned. The predictive power of the modelling hierarchy developed in MNIBS has also attracted the attention of companies keen on the large scale manufacturing of liquid crystal sensors by low cost processes such as inkjet printing. These collaborations born from MNIBS have resulted in long-lasting collaborations with industrial partners (both SMEs and large multinationals), and in the diffusion of MNIBS-related methods in industrial areas where they had been unknown up to now.
- at the microscopic (atomistic) level, the dynamic behaviour of both the liquid cruystal and the biological molecule have been studied in great detail. Phase transitions, analyte dynamics, and diffusive behaviour could be fully characterized and quantitatively described.
- at the mesoscopic level, a series of coarse-grained representations were developed based on widely differing methodologies, all of which have proved to be capable of describing LC-analyte interaction based on a few parameters extracted from the microscopic level simulations.
- at the macroscopic level, three independent and parallel routes (continuum mechanical, micro-macro, and Lattice Bolzmann) to the design of actual liquid crystal sensors have been pursued. All three have been developed to the point of practical utility.
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