View source for 4qlr


==Llama nanobody n02 raised against EAEC T6SS TssM==
<StructureSection load='4qlr' size='340' side='right'caption='[[4qlr]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[4qlr]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Lama_glama Lama glama]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4QLR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4QLR FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.7&#8491;</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4qlr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4qlr OCA], [https://pdbe.org/4qlr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4qlr RCSB], [https://www.ebi.ac.uk/pdbsum/4qlr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4qlr ProSAT]</span></td></tr>
</table>
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== Publication Abstract from PubMed ==
The type VI secretion system (T6SS) is a secretion pathway widespread in Gram-negative bacteria that targets toxins in both prokaryotic and eukaryotic cells. Although most T6SSs identified so far are involved in inter-bacterial competition, a few are directly required for full virulence of pathogens. The T6SS comprises 13 core proteins that assemble a large complex structurally and functionally similar to a phage contractile tail structure anchored to the cell envelope by a trans-membrane spanning stator. The central part of this stator, TssM, is a 1129-amino-acid protein anchored in the inner membrane that binds to the TssJ outer membrane lipoprotein. In this study, we have raised camelid antibodies against the purified TssM periplasmic domain. We report the crystal structure of two specific nanobodies that bind to TssM in the nanomolar range. Interestingly, the most potent nanobody, nb25, competes with the TssJ lipoprotein for TssM binding in vitro suggesting that TssJ and the nb25 CDR3 loop share the same TssM binding site or causes a steric hindrance preventing TssM-TssJ complex formation. Indeed, periplasmic production of the nanobodies displacing the TssM-TssJ interaction inhibits the T6SS function in vivo. This study illustrates the power of nanobodies to specifically target and inhibit bacterial secretion systems.

Inhibition of Type VI Secretion by an Anti-TssM Llama Nanobody.,Nguyen VS, Logger L, Spinelli S, Desmyter A, Le TT, Kellenberger C, Douzi B, Durand E, Roussel A, Cascales E, Cambillau C PLoS One. 2015 Mar 26;10(3):e0122187. doi: 10.1371/journal.pone.0122187., eCollection 2015. PMID:25811612<ref>PMID:25811612</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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<div class="pdbe-citations 4qlr" style="background-color:#fffaf0;"></div>

==See Also==
*[[Antibody 3D structures|Antibody 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Lama glama]]
[[Category: Large Structures]]
[[Category: Cambillau C]]
[[Category: Cascales E]]
[[Category: Desmyter A]]
[[Category: Douzi B]]
[[Category: Durand E]]
[[Category: Kellenberger C]]
[[Category: Le TTH]]
[[Category: Nguyen VS]]
[[Category: Roussel A]]
[[Category: Spinelli S]]