Truncation of the COOH-terminal region of the paramyxovirus SV5 fusion protein leads to hemifusion but not complete fusion

Sangeeta Bagai, Robert A. Lamb*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

67 Scopus citations

Abstract

The role of the simian virus 5 (SV5) fusion (F) protein 20 residue COOH- terminal region, thought to represent the cytoplasmic tail, in fusion activity was examined by constructing a series of COOH-terminal truncation mutants. When the altered for proteins were expressed in eukaryotic cells, by using the vaccinia virus-T7 transient expression system, all the for proteins exhibited similar intracellular transport properties and all were expressed abundantly on the cell surface. Quantitative and qualitative cell fusion assays indicated that all of the for protein COOH-terminal truncation mutants mediated lipid mixing with similar kinetics and efficiency as that of wild- type for protein. However, the cytoplasmic content mixing activity decreased in parallel with the extent of the deletion in the for protein COOH-terminal truncation mutants. These data indicate that it is possible to separate the presumptive early step in the fusion reaction, hemifusion, and the final stage of fusion, content mixing, and that the presence of the for protein COOH-terminal region is important for the final steps of fusion.

Original languageEnglish (US)
Pages (from-to)73-84
Number of pages12
JournalJournal of Cell Biology
Volume135
Issue number1
DOIs
StatePublished - Oct 1996

ASJC Scopus subject areas

  • Cell Biology

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