Molecular dissection of the Semliki Forest virus homotrimer reveals two functionally distinct regions of the fusion protein

Don L. Gibbons, Margaret Kielian

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Semliki Forest virus (SFV) is an enveloped alphavirus that infects cells via a membrane fusion reaction triggered by the acidic pH of endosomes. In response to low pH, the E1 proteins on the virus membrane undergo a series of conformational changes, resulting in the formation of a stable E1 homotrimer. Little is known about the structural basis of either the E1 conformational changes or the resulting homotrimer or about the mechanism of action of the homotrimer in fusion. Here, the E1 homotrimer was formed in vitro from either virus or soluble E1 ectodomain and then probed by various perturbants, proteases, or glycosidase. The preformed homotrimer was extremely stable to moderately harsh conditions and proteases. By contrast, mild reducing conditions selectively disrupted the N-terminal region of trimeric E1, making it accessible to proteolytic cleavage and producing E1 fragments that retained trimer interactions. Trypsin digestion produced a fragment missing a portion of the N terminus just proximal to the putative fusion peptide. Digestion with elastase produced several fragments with cleavage sites between residues 78 and 102, resulting in the loss of the putative fusion peptide and the release of membrane-bound E1 ectodomain as a soluble trimer. Elastase also cleaved the homotrimer within an E1 loop located near the fusion peptide in the native E1 structure. Mass spectrometry was used to map the C termini of several differentially produced and fully functional E1 ectodomains. Together, our data identify two separate regions of the SFV E1 ectodomain, one responsible for target membrane association and one necessary for trimer interactions.

Original languageEnglish (US)
Pages (from-to)1194-1205
Number of pages12
JournalJournal of Virology
Volume76
Issue number3
StatePublished - 2002

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Semliki Forest virus
Semliki forest virus
Dissection
elastase
Pancreatic Elastase
peptides
Peptides
Membranes
Digestion
Peptide Hydrolases
proteinases
digestion
Alphavirus
Viruses
viruses
Proteins
Membrane Fusion
endosomes
proteins
glycosidases

ASJC Scopus subject areas

  • Immunology

Cite this

Molecular dissection of the Semliki Forest virus homotrimer reveals two functionally distinct regions of the fusion protein. / Gibbons, Don L.; Kielian, Margaret.

In: Journal of Virology, Vol. 76, No. 3, 2002, p. 1194-1205.

Research output: Contribution to journalArticle

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