Signaling in Single Cells, Microfabricated Systems for Cellular Analysis
1979 B.S. Physics, Louisiana State University;1985 M.D., Johns Hopkins University School of Medicine; 1987 Ph.D. Medical Physics/Medical Engineering, Massachusetts Institute of Technology; 1988 Postdoctoral Fellow, Massachusetts Institute of Technology; 1989-1994 NIH Postdoctoral Fellow, Dept. of Cell Biology and Neurobiology, Stanford University; 1994-2000 Assistant Professor, Dept. of Physiology and Biophysics and Center for Biomedical Engineering, University of California-Irvine: 1995 Searle Scholar Award; 1995 Beckman Young Investigator Award; 2000-2004 Associate Professor, Dept. of Physiology and Biophysics and Dept. of Biomedical Engineering, University of California-Irvine; 2003 UCI Midcareer Research Award; 2004 UCI College of Medicine Excellence in Teaching Award; 2004-2007 Professor, Dept. of Physiology and Biophysics, and Dept. of Biomedical Engineering,University of California-Irvine; 2005-2007 Professor, Dept. of Chemistry, and Dept. of Chemical Engineering and Materials Science, University of California-Irvine; 2007-current, Distinguished Professor, Dept. of Chemistry, University of North Carolina-Chapel Hill; also Professor & Chair, UNC/NCSU Joint Department of Biomedical Engineering; Fellow, American Institute for Medical and Biological Engineering (AIMBE), 2010
Research program in the Allbritton lab is a multidisciplinary effort that brings to bear principles and techniques from chemistry, physics, engineering, and materials science to develop new assays and technologies for biomedical applications. The ongoing work in the lab comprises three major focus areas: 1) analytical techniques for single-cell biochemical assays, 2) microfabricated platforms for sorting and cloning cells, and 3) microengineered systems for recapitulating organ level function. Many of the lab’s projects and extensive collaborations within these focus areas involve the development and application of new technologies for oncology and stem cell research.
Analytical Techniques for Single-Cell Biochemical Assays
The advent of effective pharmacologic compounds targeting specific signaling pathways for clinical applications has created a demand for enzymatic assays that can be performed on single cells in disease models and patient samples. Biochemical analyses of aberrant signaling pathways are now needed to direct the best treatment option as well as to assess treatment efficacy in individual patients. The goal of this research effort is to produce the instrumentation and chemical tools needed to directly assess the catalytic activity of kinases and other signaling molecules in living cells from disease models and cancer patients.
The lab has a long history in developing novel technologies using highly sensitive analytical methods including capillary- and microfluidic-based electrophoresis. Current research efforts are directed at the design and development of biochemical substrates using peptide and lipid chemistry to create reporters of cellular signal transduction. Instrumental advances in the areas of high-throughput single-cell analysis and lab-on-a-chip platforms for cell-based assays are also an active area of research and development. The ability to identify multiple aberrant signaling pathways simultaneously in a patient’s tumor would enable individualization of multiple targeted therapies for that patient and offer the hope of developing individualized and improved therapies to supplant the existing standard of care.
Microfabricated Platforms for Sorting and Cloning Cells
The lab has pioneered the development of novel microfabricated cell-array platforms to enable the analysis and isolation of cells while they remain on a culture substrate. Cells can be monitored at single or multiple time points and selected based on a wide range of criteria including morphology, fluorescence signatures, subcellular attributes, growth properties, and other time-dependent characteristics. These arrays are produced dewetting methods to form molded rafts on a poly(dimethylsiloxane) base. Individual rafts are selectively detached employing a microneedle. These arrays can be made in almost any size, for instance millimeter-sized arrays for use with total sample sizes of hundreds to a few thousand cells (e.g. needle biopsies), to arrays of many centimeters with millions of culture sites for high-throughput screening of rare cell populations (e.g. circulating tumor cells). Numerous biomedically relevant applications of these microfabricated cell arrays are being pursued including efficient cloning of murine embryonic stem cells for improved methods to create genetically engineered animals, isolation of cytolytic T lymphocytes based on their ability to kill tumor cells, and purification of circulating tumor cells and cancer stem cells from patient samples.
Microengineered Systems for Recapitulating Organ Level Function
The ability to monitor and control the environment at the cellular and tissue level is one of the most promising applications for microengineered systems. “Organ-on-a-chip” platforms provide exquisite control of experimental variables, yet recapitulate much of the physiology of an intact organ. The lab is pursuing development and application of microTAS devices to recapitulate the microenvironments of the intestine. Purified intestinal stem cells or intestinal crypts are used to re-create on shaped arrays and contain the differentiated cell lineages as well as stem cells. Methods to create gradients across these tissues are being developed to mimic the chemical gradients thought to exist in vivo. The intestinal fluidic chips will make it feasible to combine cellular components from different genetically engineered mice for fundamental studies of intestinal biology, use in drug screening, and applications in toxicology.