The perforin pore facilitates the delivery of cationic cargos

Sarah Elizabeth Stewart, Stephanie Kondos, Antony Yaron Matthews, Michael D'Angelo, Michelle Anne Dunstone, James Whisstock, Joseph A Trapani, Phillip Ian Bird

Research output: Contribution to journalArticleResearchpeer-review

17 Citations (Scopus)

Abstract

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.
Original languageEnglish
Pages (from-to)9172 - 9181
Number of pages10
JournalJournal of Biological Chemistry
Volume289
Issue number13
DOIs
Publication statusPublished - 2014

Cite this

Stewart, Sarah Elizabeth ; Kondos, Stephanie ; Matthews, Antony Yaron ; D'Angelo, Michael ; Dunstone, Michelle Anne ; Whisstock, James ; Trapani, Joseph A ; Bird, Phillip Ian. / The perforin pore facilitates the delivery of cationic cargos. In: Journal of Biological Chemistry. 2014 ; Vol. 289, No. 13. pp. 9172 - 9181.
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abstract = "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.",
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The perforin pore facilitates the delivery of cationic cargos. / Stewart, Sarah Elizabeth; Kondos, Stephanie; Matthews, Antony Yaron; D'Angelo, Michael; Dunstone, Michelle Anne; Whisstock, James; Trapani, Joseph A; Bird, Phillip Ian.

In: Journal of Biological Chemistry, Vol. 289, No. 13, 2014, p. 9172 - 9181.

Research output: Contribution to journalArticleResearchpeer-review

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AU - Stewart, Sarah Elizabeth

AU - Kondos, Stephanie

AU - Matthews, Antony Yaron

AU - D'Angelo, Michael

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AU - Whisstock, James

AU - Trapani, Joseph A

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AB - 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.

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