A group of cell and developmental biologists requests funds for a shared facility for deconvolution microscopy.
The aim of the proposal is to provide a state-of-the-art system in which microscope, deconvolution software, computer, cameras, and environmental chamber are integrated for optimal imaging of subcellular structures in a variety of organisms. The facility is planned to provide capability for time-lapse study of live cells as well as fixed cells. FRAP capability is requested for studies of the dynamics of proteins in cells expressing GFP- tagged proteins. The applicants routinely use confocal microscopy, but for some aspects of their studies, the increased signal-to-noise possible with deconvolution will allow detection of experimental details not feasible with confocal images of their specimens. A deconvolution microscope system would open up exciting new possibilities for all of these biologists. ? ?
Sanger, Joseph W; Wang, Jushuo; Holloway, Beth et al. (2009) Myofibrillogenesis in skeletal muscle cells in zebrafish. Cell Motil Cytoskeleton 66:556-66 |
Du, Aiping; Sanger, Jean M; Sanger, Joseph W (2008) Cardiac myofibrillogenesis inside intact embryonic hearts. Dev Biol 318:236-46 |
Wang, Jushuo; Shaner, Nathan; Mittal, Balraj et al. (2005) Dynamics of Z-band based proteins in developing skeletal muscle cells. Cell Motil Cytoskeleton 61:34-48 |
Geng, Jinming; Shin, Marcus E; Gilbert, Penney M et al. (2005) Saccharomyces cerevisiae Rab-GDI displacement factor ortholog Yip3p forms distinct complexes with the Ypt1 Rab GTPase and the reticulon Rtn1p. Eukaryot Cell 4:1166-74 |