David S. Hage
Charles Bessey Professor
Hamilton Hall 704
402.472.2744
dhage@unlserve.unl.edu
Hage Research Group
Faculty & Research |
Faculty Directory |
Recent Publications | Videos | Research Story
Current Research
Our laboratory uses biological ligands in high performance liquid chromatography (HPLC) and capillary electrophoresis (CE) for the analysis of clinical, pharamaceutical, and environmental agents. One area of our work is in the use of antibodies and antibody mimics to create rapid chromatographic-based immunoassays. An example is a series of new methods we have recently created for the measuring the free, or biologically-active, fraction of drugs and hormones in blood or serum. These methods make use of antibodies with special microcolumns and supports that allow these separations to be performed in milliseconds. Similar work has been performed to create selective extraction systems and field-portable devices to isolate and analyze environmental contaminants in water.

A second area of research in our group is in the use of separation methods to study biological interactions. For example, we use immobilized proteins in HPLC columns to examine the equilibrium constants and rate constants for these proteins as they bind to drugs or other proteins in the body. This information is used to help us develop better analytical methods for these proteins and drugs or to help characterize how such agents behave in the body. The same information can be used to help develop and optimize HPLC and CE systems that employ proteins as binding agents for chiral separations.

We use various tools along with HPLC and CE to help us in our work. Part of this involves the development of new strategies for immobilizing biological ligands like proteins onto solid supports for use in HPLC systems. We are also interested in using new types of supports for this purpose, with both silica-based materials and monolithic columns being employed in our work. Various spectroscopic methods are used to help us characterize these materials, including absorbance spectroscopy, fluorescence spectroscopy, and mass spectrometry. Computer modeling and work with chromatographic theory is also utilized in our group to help us better understand the separation methods we are creating and to design new formats for these methods.


- Biochemical separations
- Bioanalytical chemistry
- Affinity chromatography
- High performance liquid chromatography
- Chromatographic immunoassays
- Biointeraction chromatography
- Drug-protein binding studies
- Biomolecule immobilization
- Monolithic columns
A graduate or postdoctoral student in my group can expect to receive training in bioanalytical chemistry and significant exposure to one or more of the following specialties: high performance liquid chromatography and affinity chromatography; capillary electrophoresis; biomolecular applications of mass spectrometry; methods for protein immobilization, modification, and characterization; separation methods for studying biological interactions; protein-based chiral separations; method development for pharmaceutical, clinical and environmental analysis; theory of chromatography and affinity-based separations.


