Wednesday, October 5, 2016

Nature Structural & Molecular Biology Contents: 2016 Volume #23 pp 871-948

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TABLE OF CONTENTS

October 2016 Volume 23, Issue 10

Editorial
News and Views
Articles
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Editorial

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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.

News and Views

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Structural basis for the poisonous activity of a predator's venom insulin   pp872 - 874
Pierre De Meyts
doi:10.1038/nsmb.3304
A potent toxin present in the venom of a fish-hunting cone snail is a minimized insulin (Con-Ins G1) lacking key residues involved in the receptor binding of most insulins. New data show that Con-Ins G1 nevertheless binds potently to the human insulin receptor, owing to a rearrangement that compensates for the lack of a critical binding residue.

See also: Article by Menting et al.

Replicating methicillin resistance?   pp874 - 875
Joshua P Ramsay
doi:10.1038/nsmb.3303
Methicillin resistance in the clinically important bacterium Staphylococcus aureus (MRSA) has evolved in multiple S. aureus lineages through acquisition of chromosomally integrating mobile genetic elements named SCCmec. Now Rice and colleagues show that the conserved SCCmec cch gene encodes an active DNA helicase, thus suggesting that extrachromosomal replication is part of the enigmatic SCCmec horizontal-transfer mechanism.

See also: Article by Mir-Sanchis et al.

Structural & Molecular Biology
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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.
 
 

Articles

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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.

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.

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

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.

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.

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

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.

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.

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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