Sandbox Reserved 818

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For that, the donor substrate used by PTX is '''NAD<sup>+</sup>''', which binds the toxin through '''Trp26''', '''Arg9''' and '''Cys41''' located in the ''active site of S1''. <br />
For that, the donor substrate used by PTX is '''NAD<sup>+</sup>''', which binds the toxin through '''Trp26''', '''Arg9''' and '''Cys41''' located in the ''active site of S1''. <br />
Concerning the acceptor substrate, it binds to the toxin through '''residues 180-219''' in the ''C-terminal region of S1''. These residues show indeed a high affinity for the G protein and are involved in the catalysis of the ADP-ribosylation. <br />
Concerning the acceptor substrate, it binds to the toxin through '''residues 180-219''' in the ''C-terminal region of S1''. These residues show indeed a high affinity for the G protein and are involved in the catalysis of the ADP-ribosylation. <br />
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In the S1 subunit, the ''catalytic residues'' '''His35''' and '''Glu129''' have been identified : His35 is involved in the ionization of the nucleophilic thiol of the cysteine residue in the G protein via its ε-N and the carboxylate group of the Glu129 side chain is in contact with the 2'-ribo-hydroxyl of the NAD<sup>+</sup>.
+
In the S1 subunit, the ''catalytic residues'' '''His35''' and '''Glu129''' have been identified: His35 is involved in the ionization of the nucleophilic thiol of the cysteine residue in the G protein via its ε-N and the carboxylate group of the Glu129 side chain is in contact with the 2'-ribo-hydroxyl of the NAD<sup>+</sup>.
==Toxic effects of pertussis toxin==
==Toxic effects of pertussis toxin==

Revision as of 15:07, 5 January 2014

This Sandbox is Reserved from 06/12/2018, through 30/06/2019 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1480 through Sandbox Reserved 1543.
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Image:1prt.png

Template:STRUCTURE 1prt

Contents

PERTUSSIS TOXIN

About this Structure

1prt is a 12 chain structure with sequence from Bordetella pertussis. The September 2005 RCSB PDB Molecule of the Month feature on Cholera Toxin by David S. Goodsell is 10.2210/rcsb_pdb/mom_2005_9. Full crystallographic information is available from OCA.


Introduction

Adding an introduction
3-7 sentences about what the protein or topic is and why it is important
first sentence should contain the name of the topic and it should be an interwiki link (so on the Hemoglobin page, you might start by writing "Hemoglobin is the protein...")
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Binding of pertussis toxin to its cellular targets

After being secreted, pertussis toxin (PTX) can interact with almost all mammalian cells, which explains the variety of biological activities of the toxin.
No specific receptors for PTX have been identified but many cell surface sialoglycoproteins are involved in the binding of PTX, together with glycoproteins: sugar moieties allow the recognition of the toxin and the carbohydrate sequence NeuAcα(2,6)-Galβ4GlcNAc is particularly important but sugar sequence alone is not sufficient.
PTX binds its target cells through the B oligomer: .

Toxin entry and trafficking in target cells

Mechanism of pertussis toxin

Pertussis toxin (PTX) acts on target cells through its A protomer which contains the enzymatically active S1 subunit.
This subunit catalyzes ADP-ribosylation of the α-subunit of trimeric G proteins, which disturbs functions of the target cells and therefore lead to various biological effects.

In facts, substrates of PTX are regulators of the membrane-bound adenylate cyclase. These G proteins bind GTP in order to transduce signals in the cell. When ADP-ribosylation by PTX occurs, the downregulation of the adenylate cyclase activity is inhibited. This inhibition leads to increase cAMP levels in cells, which explains the amount of biological activities of the toxin.

-> picture of the active site of the S1 subunit
labeled in green: key residues surrounding the NAD-binding cavity (Arg9, Trp26, Cys41)
labeled in blue: catalytic residues (His35, Glu129)

The ADP-ribosylation of trimeric G proteins occurs on a cysteine residue in the C-terminal part of the α-subunit.
For that, the donor substrate used by PTX is NAD+, which binds the toxin through Trp26, Arg9 and Cys41 located in the active site of S1.
Concerning the acceptor substrate, it binds to the toxin through residues 180-219 in the C-terminal region of S1. These residues show indeed a high affinity for the G protein and are involved in the catalysis of the ADP-ribosylation.
In the S1 subunit, the catalytic residues His35 and Glu129 have been identified: His35 is involved in the ionization of the nucleophilic thiol of the cysteine residue in the G protein via its ε-N and the carboxylate group of the Glu129 side chain is in contact with the 2'-ribo-hydroxyl of the NAD+.

Toxic effects of pertussis toxin

See Also

Reference

  • Stein PE, Boodhoo A, Armstrong GD, Cockle SA, Klein MH, Read RJ. The crystal structure of pertussis toxin. Structure. 1994 Jan 15;2(1):45-57. PMID:8075982
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