Wednesday, December 3, 2014

Nature Structural & Molecular Biology Contents: 2014 Volume #21 pp 1017-1106

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Nature Structural & Molecular Biology
TABLE OF CONTENTS

December 2014 Volume 21, Issue 12

Meeting Report
News and Views
Articles
Brief Communication
Analysis
Corrigenda
Erratum

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Meeting Report

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The Hsp90 ensemble: coordinated Hsp90-cochaperone complexes regulate diverse cellular processes   pp1017 - 1021
Serena Schwenkert, Thorsten Hugel and Marc B Cox
doi:10.1038/nsmb.2927
The Seventh International Conference on the Hsp90 Chaperone Machine took place in October 2014, in Seeon, Germany. The program highlighted recent findings in a variety of areas, including structures of heat-shock protein 90 (Hsp90)-client protein complexes, coordination of Hsp90 with cochaperones, new cellular and physiological roles for Hsp90 and therapeutic targeting of the Hsp90 ensemble for the treatment of disease and prevention of infection.

News and Views

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Dynamic activation of apoptosis: conformational ensembles of cIAP1 are linked to a spring-loaded mechanism   pp1022 - 1023
Michelle L Gill and R Andrew Byrd
doi:10.1038/nsmb.2925
cIAP1 undergoes a dramatic conformational change during activation that is now shown to be due to the dynamic and metastable nature of the closed form of the enzyme. The discovery of such a striking mechanism for functional control was enabled by state-of-the-art enzymological and biophysical methods.

See also: Article by Phillips et al.

Optimizing membrane-protein biogenesis through nonoptimal-codon usage   pp1023 - 1025
Alexey S Morgunov and M Madan Babu
doi:10.1038/nsmb.2926
Two studies provide insights into the distinct strategies used by prokaryotes and eukaryotes to pause translation in order to facilitate cotranslational targeting of membrane proteins to the translocon.

See also: Analysis by Pechmann et al.

Putting a finger in the ring   pp1025 - 1027
John McCullough and Wesley I Sundquist
doi:10.1038/nsmb.2928
Two complementary papers demonstrate that the homologous type II transmembrane proteins LAP1 and LULL1 adopt nucleotide-free AAA+ ATPase folds and donate arginine fingers to complete the active sites of Torsin AAA+ ATPases. Activated Torsin complexes appear to function in nuclear and endoplasmic reticulum membrane-remodeling processes, including a nuclear vesiculation pathway that carries large cellular and viral cargoes from the nucleus into the cytoplasm.

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Articles

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Reconstitution of active human core Mediator complex reveals a critical role of the MED14 subunit   pp1028 - 1034
Murat A Cevher, Yi Shi, Dan Li, Brian T Chait, Sohail Malik et al.
doi:10.1038/nsmb.2914
Reconstitution of a 15-subunit functional human Mediator complex establishes direct physical and functional interactions of key MED subunits with both Pol II and TFIID to support transcriptional activation and identifies subunits critical for module association and assembly.

Structural basis for membrane targeting of the BBSome by ARL6   pp1035 - 1041
André Mourão, Andrew R Nager, Maxence V Nachury and Esben Lorentzen
doi:10.1038/nsmb.2920
The BBSome is required for formation of primary cilia, sensory organelles whose dysfunction is linked to genetic disorders. Lorentzen and colleagues offer insight into BBSome membrane recruitment, providing a molecular rationale for common disease mutations.

Structural basis for interaction of a cotranslational chaperone with the eukaryotic ribosome   pp1042 - 1046
Yixiao Zhang, Chengying Ma, Yi Yuan, Jing Zhu, Ningning Li et al.
doi:10.1038/nsmb.2908
Cryo-EM structures of the co-translational chaperone RAC in association with the ribosome suggest that RAC regulates protein translation by mechanically coupling cotranslational folding with the peptide-elongation cycle.

BRD4 assists elongation of both coding and enhancer RNAs by interacting with acetylated histones   pp1047 - 1057
Tomohiko Kanno, Yuka Kanno, Gary LeRoy, Eric Campos, Hong-Wei Sun et al.
doi:10.1038/nsmb.2912
BRD4, a key target of the clinically relevant BET inhibitor JQ1, thought to function by releasing Pol II from promoter-proximal pausing, is shown to promote Pol II elongation by acting as a histone chaperone.

Stapled HIV-1 peptides recapitulate antigenic structures and engage broadly neutralizing antibodies   pp1058 - 1067
Gregory H Bird, Adriana Irimia, Gilad Ofek, Peter D Kwong, Ian A Wilson et al.
doi:10.1038/nsmb.2922
Peptide hydrocarbon stapling is used to generate protease-resistant HIV-1 MPER antigens that mimic the conformation of viral epitopes and that are recognized by two different broadly neutralizing antibodies to HIV.

Internal motions prime cIAP1 for rapid activation   pp1068 - 1074
Aaron H Phillips, Allyn J Schoeffler, Tsutomu Matsui, Thomas M Weiss, John W Blankenship et al.
doi:10.1038/nsmb.2916
Proapoptotic signals trigger the transition of cIAP1 from an autoinhibited monomeric form to an activated dimer. NMR and time-resolved SAXS analyses reveal the conformational dynamics of the cIAP1 monomer that facilitates rapid and irreversible activation.

See also: News and Views by Gill & Byrd

Cryo-EM reveals different coronin binding modes for ADP– and ADP–BeFx actin filaments   pp1075 - 1081
Peng Ge, Zeynep A Oztug Durer, Dmitri Kudryashov, Z Hong Zhou and Emil Reisler
doi:10.1038/nsmb.2907
Cryo-EM analyses of coronin in complex with F-actin in its ADP-bound or ADP–BeFx–bound state and fitting of atomic models explain the nucleotide-dependent effects of coronin on cofilin-assisted remodeling of F-actin.

Caspase-activated phosphoinositide binding by CNT-1 promotes apoptosis by inhibiting the AKT pathway   pp1082 - 1090
Akihisa Nakagawa, Kelly D Sullivan and Ding Xue
doi:10.1038/nsmb.2915
Work in Caenorhabditis elegans identifies a substrate for CED-3 caspase during apoptosis, CNT-1. The cleavage product of CNT-1 localizes to the plasma membrane and blocks the activation of AKT by PIP3, suppressing AKT's prosurvival effects.

Structural determinants of integrin β-subunit specificity for latent TGF-β   pp1091 - 1096
Xianchi Dong, Nathan E Hudson, Chafen Lu and Timothy A Springer
doi:10.1038/nsmb.2905
Integrin α-β heterodimers recognize ligands with RGD peptide motifs, but how they differentiate between the numerous RGD-containing proteins is unknown. Here, Springer and colleagues elucidate the structural basis for ligand binding specificity of the integrin β subunit.

Brief Communication

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Structure of AMP-PNP–bound BtuCD and mechanism of ATP-powered vitamin B12 transport by BtuCD–F   pp1097 - 1099
Vladimir M Korkhov, Samantha A Mireku, Dmitry B Veprintsev and Kaspar P Locher
doi:10.1038/nsmb.2918
A new crystal structure of BtuCD, a bacterial ABC transporter that uses ATP hydrolysis to drive vitamin B12 uptake, bound to an AMP-PNP nucleotide, completes the structural elucidation of intermediates in the transport cycle and reveals how ATP accelerates transport.

Analysis

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Local slowdown of translation by nonoptimal codons promotes nascent-chain recognition by SRP in vivo   pp1100 - 1105
Sebastian Pechmann, Justin W Chartron and Judith Frydman
doi:10.1038/nsmb.2919
Analyses of yeast codon usage and ribosome profiling data reveal a nonoptimal codon cluster in the mRNAs of ER-targeted proteins, downstream of the SRP-binding site, that would slow down translation to promote SRP interaction.

See also: News and Views by Morgunov & Babu

Corrigenda

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Corrigendum: mRNA-mRNA duplexes that autoelicit Staufen1-mediated mRNA decay   p1106
Chenguang Gong, Yalan Tang and Lynne E Maquat
doi:10.1038/nsmb1214-1106a

Corrigendum: Overlapping chromatin-remodeling systems collaborate genome wide at dynamic chromatin transitions   p1106
Stephanie A Morris, Songjoon Baek, Myong-Hee Sung, Sam John, Malgorzata Wiench et al.
doi:10.1038/nsmb1214-1106b

Erratum

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Erratum: An asymmetric PAN3 dimer recruits a single PAN2 exonuclease to mediate mRNA deadenylation and decay   p1106
Stefanie Jonas, Mary Christie, Daniel Peter, Dipankar Bhandari, Belinda Loh et al.
doi:10.1038/nsmb1214-1106c

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