Our research focuses on events in the exocytotic pathway that occur in the highly specialized domain of the plasma membrane-cytoplasm interface. This region is superbly imaged by total internal reflection fluorescence microscopy (TIRFM), a technique that we use extensively in our research. In the previous grant period we developed a method that combines polarization and TIRFM (P-TIRFM) to image in real time topological changes in the plasma membrane with submicron spatial resolution. We can, for the first time, directly visualize topological features of the expanding fusion pore. The proposed studies will establish a framework for the understanding of the pathways taken by the granule membrane during and after fusion.
Aim 1 will exploit the strengths of P-TIRFM as well as amperometry to study mechanisms underlying fusion pore expansion. We will study the regulation of this process by dynamin (preliminary results), synaptotagmin and granule contents (preliminary results). The dynamin studies will be empowered by the opportunity provided by Dr. Pietro De Camilli (Yale University) to investigate mouse chromaffin cells without dynamins 1 and 2 from genetically altered mice.
Aim 2 is based upon our recent findings that 1) several granule membrane proteins remain colocalized for minutes in the plasma membrane, rather than dispersing and 2) clathrin puncta formation begins within 10 sec at fusion sites. We will investigate the novel concept that granule membrane proteins that remain colocalized in the plasma membrane after exocytosis (some of which bind clathrin adaptors) induce clathrin-mediated endocytosis (CME).
Aim 3 will build upon the same preliminary results motivating Aim 2 and will determine the relationship between curvature and the progression of protein interactions in compensatory, clathrin-mediated endocytosis.
Our research focuses on the mechanisms by which hormones and neurotransmitters are secreted from cells including neurons. These processes underlie the function of the cardiovascular, endocrine and nervous systems. The process (exocytosis) occurs by the stimulated fusion of a storage vesicle or granule with the cell (plasma) membrane. We have developed powerful microscopic techniques to image these events at the cell membrane in functioning cells. The proposed new studies will help us understand the mechanism of granule membrane fusion with the cell membrane and the subsequent fate of the granule membrane. These studies have direct application to processes that are required for health and malfunction in disease.
| Weiss, Annita Ngatchou; Bittner, Mary A; Holz, Ronald W et al. (2014) Protein mobility within secretory granules. Biophys J 107:16-25 |
| Weiss, Annita Ngatchou; Anantharam, Arun; Bittner, Mary A et al. (2014) Lumenal protein within secretory granules affects fusion pore expansion. Biophys J 107:26-33 |
| Bittner, Mary A; Aikman, Rachel L; Holz, Ronald W (2013) A nibbling mechanism for clathrin-mediated retrieval of secretory granule membrane after exocytosis. J Biol Chem 288:9177-88 |
| Axelrod, Daniel (2012) Fluorescence excitation and imaging of single molecules near dielectric-coated and bare surfaces: a theoretical study. J Microsc 247:147-60 |
| Anantharam, Arun; Axelrod, Daniel; Holz, Ronald W (2012) Real-time imaging of plasma membrane deformations reveals pre-fusion membrane curvature changes and a role for dynamin in the regulation of fusion pore expansion. J Neurochem 122:661-71 |
