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ORF8a of SARS-CoV forms an ion channel: experiments and molecular dynamics simulations.

Identifieur interne : 001649 ( PubMed/Corpus ); précédent : 001648; suivant : 001650

ORF8a of SARS-CoV forms an ion channel: experiments and molecular dynamics simulations.

Auteurs : Cheng-Chang Chen ; Jens Krüger ; Issara Sramala ; Hao-Jen Hsu ; Peter Henklein ; Yi-Ming Arthur Chen ; Wolfgang B. Fischer

Source :

RBID : pubmed:20708597

English descriptors

Abstract

ORF8a protein is 39 residues long and contains a single transmembrane domain. The protein is synthesized using solid phase peptide synthesis and reconstituted into artificial lipid bilayers that forms cation-selective ion channels with a main conductance level of 8.9±0.8pS at elevated temperature (38.5°C). Computational modeling studies including multi nanosecond molecular dynamics simulations in a hydrated POPC lipid bilayer are done with a 22 amino acid transmembrane helix to predict a putative homooligomeric helical bundle model. A structural model of a pentameric bundle is proposed with cysteines, serines and threonines facing the pore.

DOI: 10.1016/j.bbamem.2010.08.004
PubMed: 20708597

Links to Exploration step

pubmed:20708597

Le document en format XML

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