4.6 Article

Structure of a Dengue Virus Envelope Protein Late-Stage Fusion Intermediate

期刊

JOURNAL OF VIROLOGY
卷 87, 期 4, 页码 2287-2293

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AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.02957-12

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  1. NIH [U54AI057159]
  2. National Institutes of Health, National Institute of General Medical Sciences [8 P41 GM103403-10]
  3. Howard Hughes Medical Institute
  4. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy (DOE) [DE-AC02-05CH11231]
  5. National Center for Research Resources [5P41RR015301-10]
  6. U.S. DOE [DE-AC02-06CH11357]

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The final stages of dengue virus fusion are thought to occur when the membrane-proximal stem drives the transmembrane anchor of the viral envelope protein (E) toward the fusion loop, buried in the target cell membrane. Crystal structures of E have lacked this essential stem region. We expressed and crystallized soluble mutant forms of the dengue virus envelope protein (sE) that include portions of the juxtamembrane stem. Their structures represent late-stage fusion intermediates. The proximal part of the stem has both intra- and intermolecular interactions, so the chain zips up along the trimer seam. The penultimate interaction we detected involves the conserved residue F402, which has hydrophobic contacts with a conserved surface on domain II. These interactions do not require any larger-scale changes in trimer packing. The techniques for expression and crystallization of sE containing stem reported here may allow further characterization of the final stages of flavivirus fusion.

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