Projects per year
Cytotoxic lymphocytes eliminate virally infected or neoplastic cells through the action of cytotoxic proteases (granzymes). The pore-forming protein perforin is essential for delivery of granzymes into the cytoplasm of target cells; however the mechanism of this delivery is incompletely understood. Perforin contains a membrane attack complex/perforin (MACPF) domain and oligomerizes to form an aqueous pore in the plasma membrane; therefore the simplest (and best supported) model suggests that granzymes passively diffuse through the perforin pore into the cytoplasm of the target cell. Here we demonstrate that perforin preferentially delivers cationic molecules while anionic and neutral cargoes are delivered inefficiently. Furthermore, another distantly related pore-forming MACPF protein, pleurotolysin (from the oyster mushroom), also favors the delivery of cationic molecules, and efficiently delivers human granzyme B. We propose that this facilitated diffusion is due to conserved features of oligomerized MACPF proteins, which may include an anionic lumen.
|Pages (from-to)||9172 - 9181|
|Number of pages||10|
|Journal||Journal of Biological Chemistry|
|Publication status||Published - 2014|
- 1 Finished
Control of proteases in infectious, degenerative and cardiovascular disease
Whisstock, J., Bird, P., Bottomley, S., Buckle, A., Pike, R. & Smith, I.
National Health and Medical Research Council (NHMRC) (Australia)
1/01/08 → 31/12/12