Our lab studies molecular and cellular mechanisms for actin assembly and actin-based cell motility. We want to understand how actin filaments assemble, how they interact with other cytoskeletal components and membranes, and how these interactions dictate cell shape and movement. The MIRA goals are: 1) combining existing grants, 2) promoting flexibility in new research directions, and 3) promoting stability and mentoring. 1) Existing Grants. Mechanisms for Transendothelial Migration is the current title of a long-standing grant focused on actin assembly and membranes. Transendothelial migration is a new area for us, one that emerged from studies on how NK cells migrate, find and kill their target cells. We are interested in how immune and cancer cells cross the endothelium of the vasculature during physiological and pathological processes. The migrating cell and the endothelial cell both actively participate, changing shape and exerting force as a result of actin filaments interacting with the plasma membrane and intracellular membranous organelles. Regulation of Actin Capping Protein is the current title of a newer grant focused on novel mechanisms of regulation of actin capping protein. Capping protein is a key regulator of the availability and activity of actin- filament barbed ends. Recent discoveries of novel regulators of capping protein have revealed unexpected insights that dramatically change our view of actin assembly in cells. We now know that regulators target capping protein to sites where cells need to assemble actin filaments and that they tune its filament-capping activity to a level that is physiologically relevant for the concentrations of the reactants and kinetics of the reactions. 2) Flexibility and New Research Directions. I have been successful in pursuing new directions, using new experimental systems, and adapting to new technologies, as described in my Biosketch. New areas for our lab in this proposal include novel connections between cytoskeleton filament systems, the use of zebrafish as a vertebrate model system, light-induced control of protein activity, and super-resolution correlative light and electron microscopy. 3) Mentoring and Stability. The MIRA FAQ mentions more time for conduct of research and mentoring junior scientists in a more stable environment, which resonates strongly with me. I enjoy serving as a mentor, and I am very proud of the success of our lab trainees and my faculty colleagues, within and outside of our department. In terms of stability, while we are grateful for our success in securing continued funding for our research, our ability to make transitions and explore new directions will be made more facile and efficient by the MIRA mechanism.
Cells change shape and move, normally and as part of various diseases. Molecules inside the cells are responsible, and we study how these molecules work. Our results are important to a wide range of diseases, including cancer, infections and arthritis.
| Johnson, Britney; McConnell, Patrick; Kozlov, Alex G et al. (2018) Allosteric Coupling of CARMIL and V-1 Binding to Capping Protein Revealed by Hydrogen-Deuterium Exchange. Cell Rep 23:2795-2804 |
| Kim, Joanna; Cooper, John A (2018) Septins regulate junctional integrity of endothelial monolayers. Mol Biol Cell 29:1693-1703 |
| Yen, Matthew; Qi, Zongtai; Chen, Xuhua et al. (2018) Transposase mapping identifies the genomic targets of BAP1 in uveal melanoma. BMC Med Genomics 11:97 |
| Kiehart, Daniel P; Cooper, John A (2018) Contractile protein biochemistry in the Pollard Lab in Baltimore. Biophys Rev 10:1483-1485 |
| Onken, Michael D; Makepeace, Carol M; Kaltenbronn, Kevin M et al. (2018) Targeting nucleotide exchange to inhibit constitutively active G protein ? subunits in cancer cells. Sci Signal 11: |
| Johnston, Adam B; Hilton, Denise M; McConnell, Patrick et al. (2018) A novel mode of capping protein-regulation by twinfilin. Elife 7: |
| Stark, Benjamin C; Lanier, M Hunter; Cooper, John A (2017) CARMIL family proteins as multidomain regulators of actin-based motility. Mol Biol Cell 28:1713-1723 |
| Santiago-Tirado, Felipe H; Onken, Michael D; Cooper, John A et al. (2017) Trojan Horse Transit Contributes to Blood-Brain Barrier Crossing of a Eukaryotic Pathogen. MBio 8: |
| Stewart-Hutchinson, Phillip J; Szasz, Taylor P; Jaeger, Emily R et al. (2017) Technical Advance: New in vitro method for assaying the migration of primary B cells using an endothelial monolayer as substrate. J Leukoc Biol 102:941-948 |
| Zhou, Julie Y; Szasz, Taylor P; Stewart-Hutchinson, Phillip J et al. (2016) L-Plastin promotes podosome longevity and supports macrophage motility. Mol Immunol 78:79-88 |
Showing the most recent 10 out of 11 publications
