Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hocine Yezid"'
Autor:
Christophe Chopard, Phuoc Bao Viet Tong, Petra Tóth, Malvina Schatz, Hocine Yezid, Solène Debaisieux, Clément Mettling, Antoine Gross, Martine Pugnière, Annie Tu, Jean-Marc Strub, Jean-Michel Mesnard, Nicolas Vitale, Bruno Beaumelle
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-15 (2018)
It is not clear whether and how incoming HIV-1 Tat accumulates in uninfected cells. Here, Chopard et al. show that, in uninfected cells, incoming Tat is palmitoylated on Cys31 by DHHC-20, which increases its affinity for PI(4,5)P2 and results in its
Externí odkaz:
https://doaj.org/article/0b76da00f3d140a9bf12b239560dc94a
Publikováno v:
Viruses, Vol 12, Iss 9, p 1025 (2020)
Bovine herpesvirus 1 (BHV-1) causes respiratory infection and abortion in cattle. Following a primary infection, BHV-1 establishes lifelong latency in the trigeminal ganglia (TG). Periodic reactivation of the latent virus in TG neurons results in ant
Externí odkaz:
https://doaj.org/article/fad4dcc06a9f4747b5509ae4eca2c863
Publikováno v:
Viruses
Volume 12
Issue 9
Viruses, Vol 12, Iss 1025, p 1025 (2020)
Volume 12
Issue 9
Viruses, Vol 12, Iss 1025, p 1025 (2020)
Bovine herpesvirus 1 (BHV-1) causes respiratory infection and abortion in cattle. Following a primary infection, BHV-1 establishes lifelong latency in the trigeminal ganglia (TG). Periodic reactivation of the latent virus in TG neurons results in ant
Publikováno v:
Virology. 548
Bovine herpesvirus envelope glycoprotein E (gE) and, in particular, the gE cytoplasmic tail (CT) is a virulence determinant in cattle. Also, the gE CT contributes to virus cell-to-cell spread and anterograde neuronal transport. In this study, our goa
Publikováno v:
Journal of Virology
Alphaherpesvirus envelope glycoprotein N (gN) and gM form a covalently linked complex. Bovine herpesvirus type 1 (BHV-1) U L 49.5 (a gN homolog) contains two predicted cysteine residues, C42 and C78. The C42 is highly conserved among the alphaherpesv
Publikováno v:
Traffic. 13:355-363
HIV-1 encodes for the small basic protein Tat (86–101 residues) that drastically enhances the efficiency of viral transcription. The mechanism enabling Tat nuclear import is not yet clear, but studies using reporter proteins fused to the Tat basic
Autor:
Hocine Yezid, Solène Debaisieux, Antoine Gross, Daniel Henaff, Simon Lachambre, Clément Mettling, Sébastien Besteiro, Christophe Chopard, Jean-Michel Mesnard, Bruno Beaumelle
Publikováno v:
Nature Communications
Nature Communications, 2015, 6 (1), pp.6211. ⟨10.1038/ncomms7211⟩
Nature Communications, Nature Publishing Group, 2015, 6 (1), ⟨10.1038/ncomms7211⟩
Nature Communications, Nature Publishing Group, 2015, 6 (1), pp.6211. ⟨10.1038/ncomms7211⟩
Nature Communications, 2015, 6 (1), pp.6211. ⟨10.1038/ncomms7211⟩
Nature Communications, Nature Publishing Group, 2015, 6 (1), ⟨10.1038/ncomms7211⟩
Nature Communications, Nature Publishing Group, 2015, 6 (1), pp.6211. ⟨10.1038/ncomms7211⟩
International audience; Most macrophages remain uninfected in HIV-1-infected patients. Nevertheless, the phagocytic capacity of phagocytes from these patients is impaired, favouring the multiplication of opportunistic pathogens. The basis for this ph
Phosphatidylinositol-(4,5)-bisphosphate enables efficient secretion of HIV-1 Tat by infected T-cells
Autor:
Françoise Sanchez, Bruno Beaumelle, Solène Debaisieux, Clément Mettling, Yea-Lih Lin, Fabienne Rayne, Anne Bonhoure, Laurence Briant, Nathalie Chazal, Hocine Yezid, Erwann P. Loret, Christian Roy, Martine Pugnière, Stefan T. Arold, Karidia Konate
Publikováno v:
EMBO Journal
EMBO Journal, EMBO Press, 2010, 29 (8), pp.1348-1362. ⟨10.1038/emboj.2010.32⟩
EMBO Journal, 2010, 29 (8), pp.1348-1362. ⟨10.1038/emboj.2010.32⟩
EMBO Journal, EMBO Press, 2010, 29 (8), pp.1348-1362. ⟨10.1038/emboj.2010.32⟩
EMBO Journal, 2010, 29 (8), pp.1348-1362. ⟨10.1038/emboj.2010.32⟩
International audience; Human immunodeficiency virus type 1 (HIV-1) transcription relies on its transactivating Tat protein. Although devoid of a signal sequence, Tat is released by infected cells and secreted Tat can affect uninfected cells, thereby
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4354dd2a3ae446c007eff4335d1dc9d
https://hal.archives-ouvertes.fr/hal-02147182/document
https://hal.archives-ouvertes.fr/hal-02147182/document
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2009, 284 (34), pp.22736-46. ⟨10.1074/jbc.M109.023705⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2009, 284 (34), pp.22736-46. ⟨10.1074/jbc.M109.023705⟩
International audience; The human immunodeficiency virus, type 1, transactivating protein Tat is a small protein that is strictly required for viral transcription and multiplication within infected cells. The infected cells actively secrete Tat using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a4d262029e77e808ef01fc5ae3d83eb
https://hal.archives-ouvertes.fr/hal-00420513
https://hal.archives-ouvertes.fr/hal-00420513
Autor:
Sylvie Brassart-Pasco, Jessica Thevenard, Nicolas Floquet, Hocine Yezid, François-Xavier Maquart, Jean-Marc Nuzillard, Laurent Ramont, Manuel Dauchez, Elise Prost, Alain J.P. Alix, Jean-Claude Monboisse
Publikováno v:
Chemistry & biology
Chemistry & biology, 2006, 13, pp.1307-1315
Chemistry & biology, 2006, 13, pp.1307-1315
We previously demonstrated that the NC1[alpha3(IV)185-191] CNYYSNS peptide inhibited in vivo tumor progression. The YSNS motif formed a beta turn crucial for biological activity. The aim of the present study was to design a YSNSG cyclopeptide with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d76e24d9c9c9f102838c20464566ee3
https://hal.archives-ouvertes.fr/hal-00134047
https://hal.archives-ouvertes.fr/hal-00134047