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Cleavage of group 1 coronavirus spike proteins: how furin cleavage is traded off against heparan sulfate binding upon cell culture adaptation

  • C.A.M. de Haan
  • , B.J. Haijema
  • , P. Schellen
  • , P.J. Wichgers Schreur
  • , E. Lintelo, te
  • , H. Vennema
  • , P.J.M. Rottier

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

A longstanding enigmatic feature of the group 1 coronaviruses is the uncleaved phenotype of their spike protein, an exceptional property among class I fusion proteins. Here, however, we show that some group 1 coronavirus spike proteins carry a furin enzyme recognition motif and can actually be cleaved, as demonstrated for a feline coronavirus. Interestingly, this feature can be lost during cell culture adaptation by a single mutation in the cleavage motif; this, however, preserves a heparan sulfate binding motif and renders infection by the virus heparan sulfate dependent. We identified a similar cell culture adaptation for the human coronavirus OC43
Original languageEnglish
Pages (from-to)6078-6083
JournalJournal of Virology
Volume82
Issue number12
DOIs
Publication statusPublished - 2008
Externally publishedYes

Keywords

  • feline infectious peritonitis
  • extended host-range
  • bacteriophage-t7 rna-polymerase
  • murine coronavirus
  • proteolytic cleavage
  • functional-characterization
  • enteric coronavirus
  • endoprotease furin
  • sars coronavirus
  • aminopeptidase-n

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