Another triple-spanning envelope protein among intracellularly budding RNA viruses: the torovirus E protein.

Another triple-spanning envelope protein among intracellularly budding RNA viruses: the torovirus E protein.
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DOI:
10.1016/0042-6822(91)90606-c
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发表时间:
1991-06
期刊:
影响因子:
3.7
通讯作者:
Rottier PJ
Rottier PJ
中科院分区:
医学3区
文献类型:
--
作者:
Den Boon JA;Snijder EJ;Locker JK;Horzinek MC;Rottier PJ

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The nucleotide sequence of the Berne virus envelope (E) protein gene was determined and its 26.5K translation product was identified by in vitro transcription and translation. Computer analysis of the protein sequence revealed the characteristics of a class III membrane protein lacking a cleaved signal sequence but containing three successive transmembrane α-helices in the N-terminal half, much the same as the coronavirus membrane (M) protein. The disposition of the E protein in the membrane was studied by in vitro translation in the presence of microsomes and by subsequent proteinase K digestion. Only small portions of either end of the polypeptide were found to be exposed on opposite sides of the vesicle membranes. Experiments with a hybrid E protein (EM) containing the C-terminal tail of a coronavirus M protein, to which an anti-peptide serum was available, showed that this C-terminus was present at the cytoplasmic side of the membrane, which is another similarity to the coronavirus M protein. Immunofluorescence experiments indicated that the EM protein, expressed by a recombinant vaccinia virus, accumulated in intracellular membranes, predominantly those of the endoplasmic reticulum. The common features of the torovirus E and the coronavirus M protein support our hypothesis that an evolutionary relationship exists between these groups of intracellularly budding viruses.
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