Tissue functional properties arise from physical and chemical processes occurring at cellular and subcellular length scales. Specifically, the physical state of tissues (e.g., osmotic and mechanical properties, state of hydration, charge density) must all be characterized on distance scales below 100 nm. Understanding the interaction of polyelectrolytes with ions represents knowledge that is critical to clarifying the basic physics of ion binding as well as physical mechanisms affecting a large number of biological processes. In biology, osmotic pressure is particularly important in regulating and mediating physiological processes. To help understand the nature of physical/chemical interactions in biomolecules and biomolecular assemblies, we have developed an experimental approach to study their structure (morphology) and thermodynamic properties simultaneously as a function of the length scale (spatial resolution) by combining macroscopic osmotic swelling pressure measurements and small-angle scattering measurements. Swelling pressure measurements probe the system in the large length scale range, thus providing information on the overall thermodynamic response. Small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS) allow us to investigate biopolymer molecules and assemblies in their natural environment and to correlate the changes in the environmental conditions (e.g., ion concentration, ion valance, pH, temperature) with physical properties such as molecular conformation and osmotic pressure. SANS and SAXS simultaneously provide information about the size of different structural elements and their respective contribution to the osmotic properties. Combining these measurements allows us to determine the length scales governing the macroscopic thermodynamic properties. This information cannot be obtained by other techniques. We have studied the effect of multivalent cations, particularly calcium ions, on the structure of various model systems mimicking soft tissues. Divalent cations are ubiquitous in the biological milieu, yet existing theories do not adequately explain their effect on and interactions with charged macromolecules. Moreover, experiments to study these interactions are difficult to perform, particularly in solution, because above a low ion concentration threshold multivalent cations generally cause phase separation or precipitation of charged molecules. Since macroscopic phase separation does not occur in cross-linked gels, we have overcome this limitation by cross-linking our biopolymers, greatly extending the range of ion concentrations over which the system remains stable. In previous studies, this new non-destructive procedure has been used to investigate cross-linked gels of a model synthetic polymer, polyacrylic acid, and different biopolymers such as DNA, hyaluronic acid and chondroitin sulfate to determine the size of the structural elements that contribute to the osmotic concentration fluctuations. We have combined SANS and SAXS to estimate the osmotic modulus of hyaluronic acid solutions in the presence of monovalent and divalent counterions. We studied the collective diffusion processes in these solutions by dynamic light scattering and determined the osmotic modulus from the relaxation response. We developed an experimental procedure to determine the distribution of counterions around charged biopolymer molecules using anomalous small-angle X-ray scattering measurements. We analyzed a series of models of network elasticity that address essential physical aspects of rigid chain biopolymer systems. Specifically, we applied our approach to understand the binding mechanism in glucose sensors made from smart zwitterionic hydrogels containing boronic acid moieties. Based on systematic SANS and osmotic pressure measurements we provided a thermodynamic explanation for the enhanced selectivity of these gels for glucose relative to fructose. This class of material has a great potential in the development of implantable continuous glucose sensors for use in diabetes. We developed a procedure to control the size, compactness and stability of DNA nanoparticles by mediating the interaction between ions and DNA. We quantified the effects of salt, pH and temperature on their stability and biological activity. These polyplexes are pathogen-like particles having a size (70 300 nm) and shape resembling spherical viruses that naturally evolved to deliver nucleic acids to the cells. They contain the pDNA in the interior surrounded by synthetic polymer bearing sugar residues on the surface recognized by the M cells and dendritic cells as pathogens. Because we can control the stability and biological activity of DNA nanoparticles, we believe that this knowledge can provide a solid foundation for developing new DNA-based vaccines for the treatment of various diseases.

Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
2012
Total Cost
$254,252
Indirect Cost
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State
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Horkay, Ferenc; Nishi, Kengo; Shibayama, Mitsuhiro (2017) Decisive test of the ideal behavior of tetra-PEG gels. J Chem Phys 146:164905
Gao, Yuan; Nieuwendaal, Ryan; Dimitriadis, Emilios K et al. (2016) Supramolecular Self-assembly of a Model Hydrogelator: Characterization of Fiber Formation and Morphology. Gels 2:
Huang, Peng; Gao, Yuan; Lin, Jing et al. (2015) Tumor-Specific Formation of Enzyme-Instructed Supramolecular Self-Assemblies as Cancer Theranostics. ACS Nano 9:9517-27
Eliav, Uzi; Komlosh, Michal E; Basser, Peter J et al. (2014) Collagen composition and content-dependent contrast in porcine annulus fibrosus achieved by using double quantum and magnetization transfer filtered UTE MRI. Magn Reson Med 71:388-93
T?ke, E R; L?rincz, O; Csiszovszki, Z et al. (2014) Exploitation of Langerhans cells for in vivo DNA vaccine delivery into the lymph nodes. Gene Ther 21:566-74
Bai, Ruiliang; Basser, Peter J; Briber, Robert M et al. (2014) NMR Water Self-Diffusion and Relaxation Studies on Sodium Polyacrylate Solutions and Gels in Physiologic Ionic Solutions. J Appl Polym Sci 131:
Chandran, Preethi L; Dimitriadis, Emilios K; Lisziewicz, Julianna et al. (2014) DNA nanoparticles with core-shell morphology. Soft Matter 10:7653-60
Gao, Yuan; Kuang, Yi; Du, Xuewen et al. (2013) Imaging self-assembly dependent spatial distribution of small molecules in a cellular environment. Langmuir 29:15191-200
L?rincz, Orsolya; T?ke, Enik? R; Somogyi, Eszter et al. (2012) Structure and biological activity of pathogen-like synthetic nanomedicines. Nanomedicine 8:497-506
Horkay, Ferenc; Basser, Peter J; Hecht, Anne-Marie et al. (2010) Counterion and pH-Mediated Structural Changes in Charged Biopolymer Gels. Macromol Symp 291-292:354-361

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