The viral G protein-coupled receptor ORF74 hijacks β-arrestins for endocytic trafficking in response to human chemokines

Research output: Contribution to journalJournal articleResearchpeer-review

  • Sabrina M. De Munnik
  • Kooistra, Albert Jelke
  • Jody Van Offenbeek
  • Saskia Nijmeijer
  • Chris De Graaf
  • Martine J. Smit
  • Rob Leurs
  • Henry F. Vischer

Kaposi's sarcoma-associated herpesvirus-infected cells express the virally encoded G protein-coupled receptor ORF74. Although ORF74 is constitutively active, it binds human CXC chemokines that modulate this basal activity. ORF74-induced signaling has been demonstrated to underlie the development of the angioproliferative tumor Kaposi's sarcoma. Whereas G protein-dependent signaling of ORF74 has been the subject of several studies, the interaction of this viral GPCR with β-arrestins has hitherto not been investigated. Bioluminescence resonance energy transfer experiments demonstrate that ORF74 recruits β-arrestins and subsequently internalizes in response to human CXCL1 and CXCL8, but not CXCL10. Internalized ORF74 traffics via early endosomes to recycling and late endosomes. Site-directed mutagenesis and homology modeling identified four serine and threonine residues at the distal end of the intracellular carboxyl-terminal of ORF74 that are required for β-arrestin recruitment and subsequent endocytic trafficking. Hijacking of the human endocytic trafficking machinery is a previously unrecognized action of ORF74.

Original languageEnglish
Article numbere0124486
JournalPLOS ONE
Volume10
Issue number4
ISSN1932-6203
DOIs
Publication statusPublished - 20 Apr 2015
Externally publishedYes

ID: 199375904