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To quantify fate-circuit dynamics in HIV, we have developed microwell 'finger' devices for long-term time-lapse imaging of donor-derived primary T cells, which are non-adherent (Razooky et al. Lab on A Chip 2012). These devices enable tracking of HIV expression dynamics in single cells over periods of > 100 hours.
Microwell Time-Lapse Microscopy
Time-Lapse Microscopy of Lymphocytes
In parallel, we are also engineering new cell-culture approaches for better in vitro control of viral infection dynamics. Recently, we demonstrated the feasibility of using acoustic forces (Jung et al. 2015, below) for high-efficiency continuous sorting of cells from viruses in fluidic devices.

Current projects focus on design, fabrication, and optimization of similar devices for long-term cell culturing and quantification of fate circuits in viruses and other biological systems.