2np0

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(New page: 200px<br /><applet load="2np0" size="450" color="white" frame="true" align="right" spinBox="true" caption="2np0, resolution 2.62&Aring;" /> '''Crystal structure of...)
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[[Image:2np0.jpg|left|200px]]<br /><applet load="2np0" size="350" color="white" frame="true" align="right" spinBox="true"
caption="2np0, resolution 2.62&Aring;" />
caption="2np0, resolution 2.62&Aring;" />
'''Crystal structure of the Botulinum neurotoxin type B complexed with synaptotagamin-II ectodomain'''<br />
'''Crystal structure of the Botulinum neurotoxin type B complexed with synaptotagamin-II ectodomain'''<br />
==Overview==
==Overview==
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Botulinum neurotoxins (BoNTs) are potent bacterial toxins that cause, paralysis at femtomolar concentrations by blocking neurotransmitter, release. A 'double receptor' model has been proposed in which BoNTs, recognize nerve terminals via interactions with both gangliosides and, protein receptors that mediate their entry. Of seven BoNTs (subtypes A-G), the putative receptors for BoNT/A, BoNT/B and BoNT/G have been identified, but the molecular details that govern recognition remain undefined. Here, we report the crystal structure of full-length BoNT/B in complex with the, synaptotagmin II (Syt-II) recognition domain at 2.6 A resolution. The, structure of the complex reveals that Syt-II forms a short helix that, binds to a hydrophobic groove within the binding domain of BoNT/B. In, addition, mutagenesis of amino acid residues within this interface on, Syt-II affects binding of BoNT/B. Structural and sequence analysis reveals, that this hydrophobic groove is conserved in the BoNT/G and BoNT/B, subtypes, but varies in other clostridial neurotoxins. Furthermore, molecular docking studies using the ganglioside G(T1b) indicate that its, binding site is more extensive than previously proposed and might form, contacts with both BoNT/B and synaptotagmin. The results provide, structural insights into how BoNTs recognize protein receptors and reveal, a promising target for blocking toxin-receptor recognition.
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Botulinum neurotoxins (BoNTs) are potent bacterial toxins that cause paralysis at femtomolar concentrations by blocking neurotransmitter release. A 'double receptor' model has been proposed in which BoNTs recognize nerve terminals via interactions with both gangliosides and protein receptors that mediate their entry. Of seven BoNTs (subtypes A-G), the putative receptors for BoNT/A, BoNT/B and BoNT/G have been identified, but the molecular details that govern recognition remain undefined. Here we report the crystal structure of full-length BoNT/B in complex with the synaptotagmin II (Syt-II) recognition domain at 2.6 A resolution. The structure of the complex reveals that Syt-II forms a short helix that binds to a hydrophobic groove within the binding domain of BoNT/B. In addition, mutagenesis of amino acid residues within this interface on Syt-II affects binding of BoNT/B. Structural and sequence analysis reveals that this hydrophobic groove is conserved in the BoNT/G and BoNT/B subtypes, but varies in other clostridial neurotoxins. Furthermore, molecular docking studies using the ganglioside G(T1b) indicate that its binding site is more extensive than previously proposed and might form contacts with both BoNT/B and synaptotagmin. The results provide structural insights into how BoNTs recognize protein receptors and reveal a promising target for blocking toxin-receptor recognition.
==About this Structure==
==About this Structure==
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2NP0 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Clostridium_botulinum Clostridium botulinum] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with ZN, CA and CL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Bontoxilysin Bontoxilysin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.69 3.4.24.69] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2NP0 OCA].
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2NP0 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Clostridium_botulinum Clostridium botulinum] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=CL:'>CL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Bontoxilysin Bontoxilysin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.69 3.4.24.69] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NP0 OCA].
==Reference==
==Reference==
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[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Arndt, J.W.]]
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[[Category: Arndt, J W.]]
[[Category: Chai, Q.]]
[[Category: Chai, Q.]]
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[[Category: Stevens, R.C.]]
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[[Category: Stevens, R C.]]
[[Category: CA]]
[[Category: CA]]
[[Category: CL]]
[[Category: CL]]
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[[Category: synaptotagamin]]
[[Category: synaptotagamin]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 12:49:30 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:09:19 2008''

Revision as of 16:09, 21 February 2008


2np0, resolution 2.62Å

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Crystal structure of the Botulinum neurotoxin type B complexed with synaptotagamin-II ectodomain

Overview

Botulinum neurotoxins (BoNTs) are potent bacterial toxins that cause paralysis at femtomolar concentrations by blocking neurotransmitter release. A 'double receptor' model has been proposed in which BoNTs recognize nerve terminals via interactions with both gangliosides and protein receptors that mediate their entry. Of seven BoNTs (subtypes A-G), the putative receptors for BoNT/A, BoNT/B and BoNT/G have been identified, but the molecular details that govern recognition remain undefined. Here we report the crystal structure of full-length BoNT/B in complex with the synaptotagmin II (Syt-II) recognition domain at 2.6 A resolution. The structure of the complex reveals that Syt-II forms a short helix that binds to a hydrophobic groove within the binding domain of BoNT/B. In addition, mutagenesis of amino acid residues within this interface on Syt-II affects binding of BoNT/B. Structural and sequence analysis reveals that this hydrophobic groove is conserved in the BoNT/G and BoNT/B subtypes, but varies in other clostridial neurotoxins. Furthermore, molecular docking studies using the ganglioside G(T1b) indicate that its binding site is more extensive than previously proposed and might form contacts with both BoNT/B and synaptotagmin. The results provide structural insights into how BoNTs recognize protein receptors and reveal a promising target for blocking toxin-receptor recognition.

About this Structure

2NP0 is a Protein complex structure of sequences from Clostridium botulinum and Mus musculus with , and as ligands. Active as Bontoxilysin, with EC number 3.4.24.69 Full crystallographic information is available from OCA.

Reference

Structural basis of cell surface receptor recognition by botulinum neurotoxin B., Chai Q, Arndt JW, Dong M, Tepp WH, Johnson EA, Chapman ER, Stevens RC, Nature. 2006 Dec 21;444(7122):1096-100. Epub 2006 Dec 13. PMID:17167418

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