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Interactions between PE2, E1, and 6K required for assembly of alphaviruses studied with chimeric viruses

Yao, Jian Sheng and Strauss, Ellen G. and Strauss, James H. (1996) Interactions between PE2, E1, and 6K required for assembly of alphaviruses studied with chimeric viruses. Journal of Virology, 70 (11). pp. 7910-7920. ISSN 0022-538X. PMCID PMC190863.

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During the assembly of alphaviruses, a preassembled nucleocapsid buds through the cell plasma membrane to acquire an envelope containing two virally encoded glycoproteins, E2 and E1. Using two chimeric viruses, we have studied interactions between E1, E2, and a viral peptide called 6K, which are required for budding. A chimeric Sindbis virus (SIN) in which the 6K gene had been replaced with that from Ross River virus (RR) produced wild-type levels of nucleocapsids and abundant PE2/E1 heterodimers that were processed and transported to the cell surface. However, only about 10% as much chimeric virus as wild-type virus was assembled, demonstrating that there is a sequence-specific interaction between 6K and the glycoproteins required for efficient virus assembly. In addition, the conformation of E1 in the E2/E1 heterodimer on the cell surface was different for the chimeric virus from that for the wild type, suggesting that one function of 6K is to promote proper folding of E1 in the heterodimer. A second chimeric SIN, in which both the 6K and E1 genes, as well as the 3' nontranslated region, were replaced with the corresponding regions of RR also resulted in the production of large numbers of intracellular nucleocapsids and of PE2/E1 heterodimers that were cleaved and transported to the cell surface. Budding of this chimera was severely impaired, however, and the yield of the chimera was only approximately 10^(-7) of the SIN yield in a parallel infection. The conformation of the SIN E2/RR E1 heterodimer on the cell surface was different from that of the SIN E2/SIN E1 heterodimer, and no interaction between viral glycoproteins and nucleocapsids at the cell plasma membrane could be detected in the electron microscope. We suggest that proper folding of the E2/E1 heterodimer must occur before the E2 tail is positioned properly in the cytoplasm for budding and before heterodimer trimerization can occur to drive virus budding.

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Additional Information:© 1996 by the American Society for Microbiology. Received 16 January 1996/Accepted 21 July 1996 We are grateful to J. E. Edens for assistance and training in electron microscopy, to Y. Shirako for stimulating discussions during the course of these experiments, and to E. Lenches for expert technical assistance. This work has been supported by grants AI 20612 and AI 10793 from NIH.
Funding AgencyGrant Number
NIHAI 20612
NIHAI 10793
Issue or Number:11
PubMed Central ID:PMC190863
Record Number:CaltechAUTHORS:YAOjvir96
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ID Code:2463
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Deposited On:04 Apr 2006
Last Modified:02 Oct 2019 22:53

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