Literature DB >> 21345958

Mobility and interactions of coronavirus nonstructural protein 4.

Marne C Hagemeijer1, Mustafa Ulasli, Annelotte M Vonk, Fulvio Reggiori, Peter J M Rottier, Cornelis A M de Haan.   

Abstract

Green fluorescent protein (GFP)-tagged mouse hepatitis coronavirus nonstructural protein 4 (nsp4) was shown to localize to the endoplasmic reticulum (ER) and to be recruited to the coronavirus replicative structures. Fluorescence loss in photobleaching and fluorescence recovery after photobleaching experiments demonstrated that while the membranes of the ER are continuous with those harboring the replicative structures, the mobility of nsp4 at the latter structures is relatively restricted. In agreement with that observation, nsp4 was shown to be engaged in homotypic and heterotypic interactions, the latter with nsp3 and nsp6. In addition, the coexpression of nsp4 with nsp3 affected the subcellular localization of the two proteins.

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Year:  2011        PMID: 21345958      PMCID: PMC3126240          DOI: 10.1128/JVI.00042-11

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  38 in total

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  31 in total

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10.  Extensive coronavirus-induced membrane rearrangements are not a determinant of pathogenicity.

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