TINE CURK GROUP
Contact:
Northwestern University
Dept. of Mat. Sci. & Eng.
2220 Campus Drive, Cook 2036
Evanston, IL 60208
email: [surname][at]northwestern.edu
Google scholar
Welcome!
I am currently a Marie Curie postdoctoral fellow at Northwestern University, working in the group of
Prof. Erik Luijten and collaborating with the group of
Prof. Samuel I. Stupp.
Education:
Charge regulation in molecules, polyelectrolytes and nanoparticles
Nanoparticles, polyelectrolytes and biomolecules in solution acquire charge through the dissociation or association of surface groups. Thus, a proper description of their electrostatic interactions requires sampling of protonation states and the use of charge-regulating boundary conditions rather than the commonly employed constant-charge approximation. Charge regulation effects can qualitatively change structures due to global charge redistribution, stabilizing asymmetric constructs. We provide an open-source implementation of the charge-regulation solver for the LAMMPS molecular dynamics package.
Optimal packing of polymers (DNA) in viral capsids.
Although the free energy of a genome packing into a virus is dominated by DNA-DNA interactions, ordering of the DNA inside the capsid is elasticity driven, suggesting general solutions with DNA organized into spool-like domains. Using analytical calculations and computer simulations of a long elastic filament confined to a spherical container, we show that the ground state is not a single spool as assumed hitherto, but an ordering mosaic of multiple homogeneously ordered domains. At low densities, we observe concentric spools, while at higher densities, other morphologies emerge, which resemble topological links.
Designing superselective targeting in multivalent polymers
We rationalized design rules for super-selective targeting using multivalent polymers, in collaboration with Dr. Galina Dubacheva at ENS Paris-Saclay and Prof. Ralf Richter at Leeds. We have also improved the sequence design of nucleotide probes for pathogen genome detection in collaboration with Prof. Rosalind J. Allen at Edinburgh
Designing multivalent interactions
Interactions with multicomponent membranes are difficult to predict due to Here we analytically derived design rules for multicomponent interactions and, supported by Monte Carlo simulations, demonstrated a general route towards targeting multicomponent cell membranes. We also show the effect of intrinsic curvature of receptors, in collaboration with Andjela Saric at UCL. Work on immune response via activation of TLR9 receptors by multivalent DNA--peptide aggregates led to a breakthrough in our understanding of immune system activation by DNA-peptide complexes on the cellular level and points to a physical origin of certain autoimmune diseases like Psoriasis. In collaboration with the experimental group of Gerard Wong at UCLA,
Phase behavior of polymer–nanoparticle composites
We showed how confining nanoparticles to polymer brushes leads to microphase separation and pattern formation. Patterns can be controlled by external fields, thus opening up new routes for the design of thin structured films.