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TABLE OF CONTENTS
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October 2016 Volume 23, Issue 10 |
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 | Editorial News and Views Articles |  | Advertisement |  |  |  | nature.com webcasts Springer Nature presents a custom webcast on Advancements in single-cell RNA-seq: differential expression analysis and immune profiling November 3, 2016; 9AM PDT, 12PM EDT, 4PM GMT, 5PM CET Learn about the latest advancements in single-cell RNA-seq and its application in whole transcriptome analysis and immune profiling. Register for FREE Sponsored by Takara Bio USA, Inc. | |
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nature.com webcasts Springer Nature presents a custom webcast on: Optimizing sensitivity and specificity in the RT-QuIC assay using BMG plate readers Date: Wednesday October 19, 2016 Time: 8AM PDT, 11AM EDT, 4PM BST, 5PM CEST Register for FREE at And learn how the RT-QuIC assay is currently being used as a diagnostic in the clinical setting for CJD and has the potential to be a valuable screening tool. Sponsored by: BMG LABTECH | | |
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Cell Death & Disease is an online-only, open access journal seeking to promote diverse and integrated areas of experimental and internal medicine with its specialities, including cancer, cancer metabolism, immunity and neuroscience.
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Where are the data? p871 doi:10.1038/nsmb.3307 Here, we announce two policy changes across Nature journals: data-availability statements in all published papers and official Worldwide Protein Data Bank (wwPDB) validation reports for peer review. |
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News and Views | Top |
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Nature Insight: The Protein World This Insight highlights four exciting topics in contemporary protein science: de novo designed proteins; how cells monitor and regulate the proteome; the rise of cryo-electron microscopy; and proteome analysis through high-resolution mass spectrometry. | | |
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Protecting genome integrity during CRISPR immune adaptation pp876 - 883 Addison V Wright and Jennifer A Doudna doi:10.1038/nsmb.3289 Cas1-Cas2 integrase achieves full-site integration only for proper targets and protospacers, whereas at non-CRISPR sites, integration stalls at the half-site intermediate, thereby protecting host genome integrity during CRISPR immune adaptation. |
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Membrane insertion of a Tc toxin in near-atomic detail pp884 - 890 Christos Gatsogiannis, Felipe Merino, Daniel Prumbaum, Daniel Roderer, Franziska Leidreiter et al. doi:10.1038/nsmb.3281 A cryo-EM structure of toxin component TcdA1 embedded in lipid nanodiscs reveals details of the mechanism used by this bacterial toxin to insert into the host cell membrane. |
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Staphylococcal SCCmec elements encode an active MCM-like helicase and thus may be replicative pp891 - 898 Ignacio Mir-Sanchis, Christina A Roman, Agnieszka Misiura, Ying Z Pigli, Susan Boyle-Vavra et al. doi:10.1038/nsmb.3286 One of the conserved proteins of the Staphylococcus aureus mobile genomic island responsible for methicillin resistance is an active MCM-like helicase, thus suggesting replication that would enhance the efficiency of horizontal gene transfer.
See also: News and Views by Ramsay |
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Glycan shield and epitope masking of a coronavirus spike protein observed by cryo-electron microscopy pp899 - 905 Alexandra C Walls, M Alejandra Tortorici, Brandon Frenz, Joost Snijder, Wentao Li et al. doi:10.1038/nsmb.3293 Cryo-EM and mass spectrometry analyses of the spike glycoprotein trimer from coronavirus HcoV-NL63 reveal an extensive glycan shield that covers the protein surface, including an epitope targeted by neutralizing antibodies against several coronaviruses. |
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Natively glycosylated HIV-1 Env structure reveals new mode for antibody recognition of the CD4-binding site pp906 - 915 Harry B Gristick, Lotta von Boehmer, Anthony P West Jr, Michael Schamber, Anna Gazumyan et al. doi:10.1038/nsmb.3291 Crystal structures of HIV Env trimer with native glycosylation in complex with neutralizing antibodies reveal a glycan shield of high-mannose and complex-type N-glycan and indicate a path for germline-targeting vaccine design. |
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A minimized human insulin-receptor-binding motif revealed in a Conus geographus venom insulin pp916 - 920 John G Menting, Joanna Gajewiak, Christopher A MacRaild, Danny Hung-Chieh Chou, Maria M Disotuar et al. doi:10.1038/nsmb.3292 Structural elucidation and biochemical analysis of a cone snail insulin venom that binds and activates the human insulin receptor may permit design of ultrafast-acting insulin analogs for diabetes therapy.
See also: News and Views by De Meyts |
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A molecular code for endosomal recycling of phosphorylated cargos by the SNX27-retromer complex pp921 - 932 Thomas Clairfeuille, Caroline Mas, Audrey S M Chan, Zhe Yang, Maria Tello-Lafoz et al. doi:10.1038/nsmb.3290 A systematic analysis reveals that acidic or phosphorylated residues upstream of the PDZ-binding motif contribute to efficient recognition of cargos by the SNX27 PDZ domain, thus leading to the identification of hundreds of potential new SNX27 ligands. |
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The DDB1-DCAF1-Vpr-UNG2 crystal structure reveals how HIV-1 Vpr steers human UNG2 toward destruction pp933 - 940 Ying Wu, Xiaohong Zhou, Christopher O Barnes, Maria DeLucia, Aina E Cohen et al. doi:10.1038/nsmb.3284 The crystal structure of HIV-1 accessory protein Vpr in complex with human UNG2 and DDB1-DCAF1 provides insight into how the viral protein directs UNG2 for degradation. |
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Methyl transfer by substrate signaling from a knotted protein fold pp941 - 948 Thomas Christian, Reiko Sakaguchi, Agata P Perlinska, Georges Lahoud, Takuhiro Ito et al. doi:10.1038/nsmb.3282 The structurally constrained knotted configuration of the RNA methyltransferase TrmD captures the free energy of substrate binding to facilitate catalysis. |
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