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Items: 1 to 20 of 74

1.
2.

Role of endocytosis and low pH in murine hepatitis virus strain A59 cell entry.

Eifart P, Ludwig K, Böttcher C, de Haan CA, Rottier PJ, Korte T, Herrmann A.

J Virol. 2007 Oct;81(19):10758-68. Epub 2007 Jul 11.

3.

Cleavage of group 1 coronavirus spike proteins: how furin cleavage is traded off against heparan sulfate binding upon cell culture adaptation.

de Haan CA, Haijema BJ, Schellen P, Wichgers Schreur P, te Lintelo E, Vennema H, Rottier PJ.

J Virol. 2008 Jun;82(12):6078-83. doi: 10.1128/JVI.00074-08. Epub 2008 Apr 9.

4.

Structural basis for coronavirus-mediated membrane fusion. Crystal structure of mouse hepatitis virus spike protein fusion core.

Xu Y, Liu Y, Lou Z, Qin L, Li X, Bai Z, Pang H, Tien P, Gao GF, Rao Z.

J Biol Chem. 2004 Jul 16;279(29):30514-22. Epub 2004 Apr 27.

6.

Furin cleavage of the SARS coronavirus spike glycoprotein enhances cell-cell fusion but does not affect virion entry.

Follis KE, York J, Nunberg JH.

Virology. 2006 Jul 5;350(2):358-69. Epub 2006 Mar 7.

7.

Furin processing and proteolytic activation of Semliki Forest virus.

Zhang X, Fugère M, Day R, Kielian M.

J Virol. 2003 Mar;77(5):2981-9.

9.

A second SARS-CoV S2 glycoprotein internal membrane-active peptide. Biophysical characterization and membrane interaction.

Guillén J, Pérez-Berná AJ, Moreno MR, Villalaín J.

Biochemistry. 2008 Aug 5;47(31):8214-24. doi: 10.1021/bi800814q. Epub 2008 Jul 11.

PMID:
18616295
10.

Proteolytic activation of tick-borne encephalitis virus by furin.

Stadler K, Allison SL, Schalich J, Heinz FX.

J Virol. 1997 Nov;71(11):8475-81.

11.

Prototype foamy virus envelope glycoprotein leader peptide processing is mediated by a furin-like cellular protease, but cleavage is not essential for viral infectivity.

Duda A, Stange A, Lüftenegger D, Stanke N, Westphal D, Pietschmann T, Eastman SW, Linial ML, Rethwilm A, Lindemann D.

J Virol. 2004 Dec;78(24):13865-70.

12.

Severe acute respiratory syndrome coronavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides.

Bosch BJ, Martina BE, Van Der Zee R, Lepault J, Haijema BJ, Versluis C, Heck AJ, De Groot R, Osterhaus AD, Rottier PJ.

Proc Natl Acad Sci U S A. 2004 Jun 1;101(22):8455-60. Epub 2004 May 18.

13.
14.

The carbohydrate-binding plant lectins and the non-peptidic antibiotic pradimicin A target the glycans of the coronavirus envelope glycoproteins.

van der Meer FJ, de Haan CA, Schuurman NM, Haijema BJ, Verheije MH, Bosch BJ, Balzarini J, Egberink HF.

J Antimicrob Chemother. 2007 Oct;60(4):741-9. Epub 2007 Aug 18.

PMID:
17704516
15.

Spike protein assembly into the coronavirion: exploring the limits of its sequence requirements.

Bosch BJ, de Haan CA, Smits SL, Rottier PJ.

Virology. 2005 Apr 10;334(2):306-18.

16.

Palmitoylation of the cysteine-rich endodomain of the SARS-coronavirus spike glycoprotein is important for spike-mediated cell fusion.

Petit CM, Chouljenko VN, Iyer A, Colgrove R, Farzan M, Knipe DM, Kousoulas KG.

Virology. 2007 Apr 10;360(2):264-74. Epub 2006 Nov 28.

17.

Genetic analysis of the SARS-coronavirus spike glycoprotein functional domains involved in cell-surface expression and cell-to-cell fusion.

Petit CM, Melancon JM, Chouljenko VN, Colgrove R, Farzan M, Knipe DM, Kousoulas KG.

Virology. 2005 Oct 25;341(2):215-30. Epub 2005 Aug 15.

19.

Protease-mediated entry via the endosome of human coronavirus 229E.

Kawase M, Shirato K, Matsuyama S, Taguchi F.

J Virol. 2009 Jan;83(2):712-21. doi: 10.1128/JVI.01933-08. Epub 2008 Oct 29.

20.

Coronavirus escape from heptad repeat 2 (HR2)-derived peptide entry inhibition as a result of mutations in the HR1 domain of the spike fusion protein.

Bosch BJ, Rossen JW, Bartelink W, Zuurveen SJ, de Haan CA, Duquerroy S, Boucher CA, Rottier PJ.

J Virol. 2008 Mar;82(5):2580-5. Epub 2007 Dec 12.

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