6idl

<table><tr><td colspan='2'>[[6idl]] is a 9 chain structure with sequence from [https://en.wikipedia.org/wiki/Dengue_virus_3 Dengue virus 3] and [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6IDL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6IDL FirstGlance]. <br>

</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=6idl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6idl OCA], [https://pdbe.org/6idl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6idl RCSB], [https://www.ebi.ac.uk/pdbsum/6idl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6idl ProSAT]</span></td></tr>

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== Publication Abstract from PubMed ==

Dengue virus (DENV) particles are released from cells in different maturation states. Fully immature DENV (immDENV) is generally non-infectious, but can become infectious when complexed with anti-precursor membrane (prM) protein antibodies. It is unknown how anti-prM antibody-coated particles can undergo membrane fusion since the prM caps the envelope (E) protein fusion loop. Here, we determined cryoelectron microscopy (cryo-EM) maps of the immDENV:anti-prM complex at different pH values, mimicking the extracellular (pH 8.0) or endosomal (pH 5.0) environments. At pH 5.0, there are two structural classes with fewer antibodies bound than at pH 8.0. These classes may represent different maturation states. Molecular simulations, together with the measured high-affinity pr:antibody interaction (versus the weak pr:E interaction) and also the low pH cryo-EM structures, suggest how antibody:pr complex can dislodge from the E protein at low pH. This exposes the E protein fusion loop enhancing virus interaction with endosomes.

 

Mechanism of Enhanced Immature Dengue Virus Attachment to Endosomal Membrane Induced by prM Antibody.,Wirawan M, Fibriansah G, Marzinek JK, Lim XX, Ng TS, Sim AYL, Zhang Q, Kostyuchenko VA, Shi J, Smith SA, Verma CS, Anand G, Crowe JE Jr, Bond PJ, Lok SM Structure. 2018 Oct 30. pii: S0969-2126(18)30370-8. doi:, 10.1016/j.str.2018.10.009. PMID:30471923<ref>PMID:30471923</ref>

 

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>

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<references/>

[[Category: Human]]

[[Category: Fibriansah, G]]

[[Category: Kostyuchenko, V A]]

[[Category: Lok, S M]]

[[Category: Ng, T S]]

[[Category: Shi, J]]

[[Category: Wirawan, M]]

[[Category: Zhang, Q]]

[[Category: Virus]]