- Pore forming toxins
Pore forming toxins (PFTs) are
protein toxins, typically, (but not exclusively) produced by bacteria, such as "C.perfringens" and "S.aureus". They are frequently cytotoxic(i.e., they kill cells) as they create unregulated pores in the membrane of targeted cells.
Types of PFTs
PFTs can be divided into the following subcategories:
* Beta-pore forming toxins
** eg. α-
* Binary toxins
* Cholesterol-dependent cytolysins (CDCs)
** eg. Pneumolysin
* Small pore-forming toxins
Beta-pore forming toxins
β-PFTs are so-named because of their structural characteristics: they are composed mostly of β-strand-based domains. Whilst they frequently have divergent sequences, X-ray crystallographic structures have revealed some commonalities: α-haemolysin [Song L, Hobaugh MR, Shustak C, Cheley S, Bayley H, Gouaux JE Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore Science v274, p.1859-1866] and
Panton-Valentine leukocidinS [Guillet V, Roblin P, Werner S, Coraiola M, Menestrina G, Monteil H, Prevost G, Mourey L Crystal structure of leucotoxin S component: new insight into the Staphylococcal beta-barrel pore-forming toxins J. Biol. Chem. v279, p.41028-41037] are structurally related, as are aerolysin [Parker MW, Buckley JT, Postma JP, Tucker AD, Leonard K, Pattus F, Tsernoglou D Structure of the Aeromonas toxin proaerolysin in its water-soluble and membrane-channel states Nature v367, p.292-295] and Clostridial Epsilon-toxin [Cole AR, Gibert M, Popoff M, Moss DS, Titball RW, Basak AK Clostridium perfringens epsilon-toxin shows structural similarity to the pore-forming toxin aerolysin Nat Struct Mol Biol v11, p.797-798] .
Mode of action
β-PFTs are dimorphic proteins that exist as soluble
monomersand then assemble to form multimericassemblies that constitute the pore. Fig 1 shows the pore-form of α- Hemolysin, the only crystal structure of a β-PFT in its pore-form to-date. 7 α-Hemolysin monomers come together to create the mushroom-shaped pore. The 'cap' of the mushroom sits on the surface of the cell, and the 'stalk' of the mushroom penetrates the cell membrane, rendering it permeable (see later). The 'stalk' is composed of a 14-strand β-barrel, with two strands donated from each monomer. The Panton-Valentine Leucocidin S structure (PDB 1T5R) shows a highly related structure, but in its soluble monomeric state. This shows that the strands involved in forming the 'stalk' are in a very different conformation- shown in Fig 2.
The transition between soluble monomer and membrane associated heptamer is not a trivial one: it is believed that β-PFTs, follow as similar assembly pathway as the CDCs (see Cholesterol-dependent cytolysins later), in that they must first assemble on the cell-surface (in a receptor-mediated fashion in some cases) in a pre-pore state. Following this, the large-scale conformational change occurs in which the membrane spanning section is formed and inserted into the membrane.
Some β-PFTs such as clostridial ε-toxin and
Clostridium perfringensEnterotoxin (CPE) bind to the cell membrane via specific receptors - possibly certain claudins for CPE [Fujita K, Katahira J, Horiguchi Y, Sonoda N, Furuse M, Tsukita S. Clostridium perfringens enterotoxin binds to the second extracellular loop of claudin-3, a tight junction integral membrane protein."FEBS Lett". 2000 Jul 7;476(3):258-61. ] , possibly GPI anchors or other sugars for ε-toxin - these receptors help raise the local concentration of the toxins, allowing oligomerisation and pore formation.
The Cyto-lethal effects of the pore
When the pore is formed, the tight regulation of what can and cannot enter/leave a cell is disrupted. Ions and small molecules, such as
amino acidsand nucleotideswithin the cell flow out, and water from the surrounding tissue enters. The loss of important small molecules to the cell can disrupt protein synthesisand other crucial cellular reactions. The loss of ions, especially calciumcan cause cell signallingpathways to be spuriously activated or deactivated. The uncontrolled entry of water into a cell can cause the cell to swell up uncontrollably: initially, this causes a process called blebbing, where large parts of the cell membrane are distorted and give way under the mounting internal pressure. Ultimately this can cause the cell to burst.
"See the main article for more information on
Binary toxins [Barth, H "et al", Binary Bacterial Toxins: Biochemistry, Biology, and Applications of common "Clostridium" and "Bacillus" Proteins, (2004), "Micro. Mole. Biol. Rev. 68, p373] , such as
Anthraxlethal & edema toxins, "C.perfringens" Iota toxin and "C.difficile" cyto-lethal toxins consist of two components (hence "binary"):
* an emzymatic component - A
* a membrane-altering component - B
The B component facilitates the entry of the enzymatic 'payload' into the target cell, by forming homomeptameric pores, as shown above for βPFTs. The A component then enters the
cytosoland inhibits normal cell functions by one of the following means:
ADP-Ribosylation is a common enzymatic methods used by various bacterial toxins from various species. These toxins (including "C.perfringens" Iota toxin & "C.Botulinum C2 toxin) attach a ribosyl-ADP moiety to surface
Arginineresidue 117 of G-actin. This prevents G-actin assembling to form F-actin, and thus the cytoskeletonbreaks down, resulting in cell death.
Proteolysisof Mitogen-activated protein kinase kinases (MAPKK)=
The A component of
Anthrax toxinlethal toxin is zinc-metallo proteasewhich shows specificity for a conserved family of Mitogen-activated protein kinase kinases. The loss of these proteins results in a breakdown of cell signalling which in turn renders the cell insensitive to outside stimuli - therefore no immune responseis triggered.
intracellularlevels of cAMP Anthrax toxinEdema toxin triggers a calciumion influx into the target cell. This subsequently elevates intracellular cAMP levels. This can profoundly alter any sort of immune response, by inhibiting leucocyteproliferation, phagocytosisand pro inflammatory cytokinerelease.
CDCs, such as pneumolysin, from "S.pneumoniae", form pores as large as 260Å (26nm), containing between 30 and 44 monomer units. [S.J. Tilley, E.V. Orlova, R.J.C. Gilbert, P.W. Andrew and H.R. Saibil, Structural Basis of Pore Formationby the Bacterial Toxin Pneumolysin (2005) Cell 121 , pp. 247–256.]
Electron Microscopystudies of Pneumolysin show that it assembles into large multimeric peripheral membrane complexes before undergoing a conformational change in which a group of α-helices in each monomer change into extended, amphipathicβ-hairpins that span the membrane, in a manner reminiscent of α-haemolysin, albeit on a much larger scale (Fig 3). CDCs are homologous to the MACPFfamily of pore forming toxins and it is suggested that both families utilise a common mechanism (Fig 4).cite journal |author=Carlos J. Rosado, Ashley M. Buckle, Ruby H. P. Law, Rebecca E. Butcher, Wan-Ting Kan, Catherina H. Bird, Kheng Ung, Kylie A. Browne, Katherine Baran, Tanya A. Bashtannyk-Puhalovich, Noel G. Faux, Wilson Wong, Corrine J. Porter, Robert N. Pike, Andrew M. Ellisdon, Mary C. Pearce, Stephen P. Bottomley, Jonas Emsley, A. Ian Smith, Jamie Rossjohn, Elizabeth L. Hartland, Ilia Voskoboinik, Joseph A. Trapani, Phillip I. Bird, Michelle A. Dunstone, and James C. Whisstock |title=A Common Fold Mediates Vertebrate Defense and Bacterial Attack |journal=Science |year=2007, |doi=10.1126/science.1144706 |volume=317 |pages=1548 |pmid=17717151] [http://www.rcsb.org/pdb/explore/explore.do?structureId=2QP2] Eukaryote MACPFproteins function in immune defence and are found in proteins such as perforin and complement C9. [cite journal |author=Tschopp J, Masson D, Stanley KK |title=Structural/functional similarity between proteins involved in complement- and cytotoxic T-lymphocyte-mediated cytolysis |journal=Nature |volume=322 |issue=6082 |pages=831–4 |year=1986 |pmid=2427956 |doi=10.1038/322831a0]
mall pore-forming toxins
Q. Bacteria can invest an awful lot of time and energy in making these toxins: CPE can account for up to 15% of the dry mass of "C.perfringens" at the time of
sporulation, so why bother? : A(1). Food. After the target cell has ruptured and released its contents, the bacteria can scavenge the remains for nutrients.: A(2). Environment. The mammalian immune responsehelps create the anaerobic environment that anaerobic bacteria require.
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