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2015/06/30

Nature Methods Contents: July 2015 Volume 12 pp 587 - 692

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Nature Methods


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TABLE OF CONTENTS

July 2015 Volume 12, Issue 7

In This Issue
Editorial
This Month
Correspondence
Research Highlights
Commentary
Technology Feature
News and Views
Perspective
Analysis
Brief Communications
Articles
Corrigenda
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In This Issue

Top

In This Issue   

Editorial

Top

Summer reading: popular science and 'lab lit'   p587
doi:10.1038/nmeth.3474
An idiosyncratic selection of science-themed books for the summer.

This Month

Top

The Author File: Stefan Kappe   p589
Vivien Marx
doi:10.1038/nmeth.3445
A way to generate recombinant progeny of Plasmodium falciparum for genetics experiments, and the virtues of scuba diving.

Points of View: Unentangling complex plots   p591
Gregor McInerny and Martin Krzywinski
doi:10.1038/nmeth.3451
Carefully designed subplots scaled to the data are often superior to a single complex overview plot.

Correspondence

Top

iSMS: single-molecule FRET microscopy software   pp593 - 594
Søren Preus, Sofie L Noer, Lasse L Hildebrandt, Daniel Gudnason and Victoria Birkedal
doi:10.1038/nmeth.3435

InferenceMAP: mapping of single-molecule dynamics with Bayesian inference   pp594 - 595
Mohamed El Beheiry, Maxime Dahan and Jean-Baptiste Masson
doi:10.1038/nmeth.3441

Chemically defined, albumin-free human cardiomyocyte generation   pp595 - 596
Xiaojun Lian, Xiaoping Bao, Misha Zilberter, Mattias Westman, André Fisahn et al.
doi:10.1038/nmeth.3448

Research Highlights

Top

Catching Pol II in the act
Two methods capture the pausing behavior of RNA polymerase II as it generates messages from mammalian genomes.

A machine to manage modifications
An automated platform mass-produces RNAs incorporating a wide variety of precisely positioned chemical alterations.

Cryo-EM goes high-resolution
The highest-resolution structure solved by cryo-electron microscopy to date reveals what it takes to reach the resolution realm of X-ray crystallography.

Reproducibly generating organ buds in vitro
Coculture of three cell types on hydrogel with the appropriate stiffness enables the generation of functional organ buds.

Chemogenetic manipulation of neurons
The family of designer receptors now includes an orthogonally activated member for multiplexed chemogenetic control of neural activity.

Methods in Brief

Inhibition with BOLT | Chromatin accessibility in single cells | RNA structure by solid-state NMR | A high-throughput platform for studying chemotaxis

Tools in Brief

Optogenetic access to opioid signaling | Sub-primed pluripotent stem cells | Efficient transduction of proteins into eukaryotic cells | Neurons on the blink

Methods
JOBS of the week
Postdoctoral researcher: Simulations of the properties and morphology of polymers
KU Leuven
Scientia Fellows – 2nd Call: Marie Curie Postdoctoral Fellowships in Health Sciences
University of Oslo
Two PhD positions – Systems Biology / Bioinformatics / Computational Biology
University of Regina
PhD position Pathways of nanoparticle uptake and trafficking by cells (1.0 fte)
Rijksuniversiteit Groningen
Postdoctoral Training Fellowship in Cancer Genomics
The Francis Crick Institute
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Methods
EVENT
SMODIA "Statistical Methods for Omics Data Integration and Analysis 2015"
14th Sept - 16th Sept 2015
Valencia, Spain
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Commentary

Top

Mass spectrometrists should search only for peptides they care about   pp605 - 608
William Stafford Noble
doi:10.1038/nmeth.3450
A Commentary proposes that in order to improve statistical power in mass spectrometry-based proteomics data analysis, irrelevant peptides should be removed from the database prior to searching.

Technology Feature

Top

Metabolism: feeding fruit flies   pp609 - 612
Vivien Marx
doi:10.1038/nmeth.3443
Measuring how much a fruit fly eats opens the door to studies of metabolism and aging. But the assays are hotly debated.

News and Views

Top

Co-opting CRISPR to deliver functional RNAs   pp613 - 614
Pei-Chun Lin and Jacob E Corn
doi:10.1038/nmeth.3452
Portions of the CRISPR-Cas9 guide RNA can be reworked to carry functional RNA cargos to genomic loci.

See also: Article by Shechner et al.

Perspective

Top

Pathway and network analysis of cancer genomes   pp615 - 621
Pau Creixell, Jüri Reimand, Syed Haider, Guanming Wu, Tatsuhiro Shibata, Miguel Vazquez, Ville Mustonen, Abel Gonzalez-Perez, John Pearson, Chris Sander, Benjamin J Raphael, Debora S Marks, B F Francis Ouellette, Alfonso Valencia, Gary D Bader, Paul C Boutros, Joshua M Stuart, Rune Linding, Nuria Lopez-Bigas and Lincoln D Stein for the Mutation Consequences and Pathway Analysis working group of the International Cancer Genome Consortium
doi:10.1038/nmeth.3440
International Cancer Genome Consortium members review and recommend approaches to pathway and network analysis to uncover molecular processes that contribute to tumor biology.

Analysis

Top

Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection OPEN   pp623 - 630
Adam D Ewing, Kathleen E Houlahan, Yin Hu, Kyle Ellrott, Cristian Caloian et al.
doi:10.1038/nmeth.3407
The first report of the ICGC-TCGA DREAM Somatic Mutation Calling Challenge introduces the BAMSurgeon tool for accurate tumor simulation and reports the performance of 248 submissions in calling single-nucleotide variants from three pairs of synthetic tumor-normal genome benchmarks.

Brief Communications

Top

Plasmodium falciparum genetic crosses in a humanized mouse model   pp631 - 633
Ashley M Vaughan, Richard S Pinapati, Ian H Cheeseman, Nelly Camargo, Matthew Fishbaugher et al.
doi:10.1038/nmeth.3432
A human-liver chimeric mouse supports the growth of recombinant Plasmodium falciparum progeny, enabling easy analysis of genetic crosses between parasite strains.

Structural analysis of multicellular organisms with cryo-electron tomography   pp634 - 636
Jan Harapin, Mandy Börmel, K Tanuj Sapra, Damian Brunner, Andres Kaech et al.
doi:10.1038/nmeth.3401
Tissues from multicellular organisms can be imaged by cryo-electron tomography using an optimized combination of vitrification, milling and application of fiducial markers.

Functional differentiation of human pluripotent stem cells on a chip   pp637 - 640
Giovanni G Giobbe, Federica Michielin, Camilla Luni, Stefano Giulitti, Sebastian Martewicz et al.
doi:10.1038/nmeth.3411
This paper shows that microfluidic perfusion frequency can be optimized to improve the differentiation of human pluripotent stem cells along different lineages, and uses this principle to achieve functional hPSC differentiation directly on a chip.

3D high- and super-resolution imaging using single-objective SPIM   pp641 - 644
Remi Galland, Gianluca Grenci, Ajay Aravind, Virgile Viasnoff, Vincent Studer et al.
doi:10.1038/nmeth.3402
Light-sheet microscopy using a single objective and micromirrors to orient the light sheet enables high- and super-resolution imaging of cells and embryos on a standard microscope.

In vivo single-cell labeling by confined primed conversion   pp645 - 648
William P Dempsey, Lada Georgieva, Patrick M Helbling, Ali Y Sonay, Thai V Truong et al.
doi:10.1038/nmeth.3405
Primed conversion of proteins such as Dendra2 confines photoconversion to a limited 3Dvolume through a sequential absorption process relying on illumination with two separate low-intensity lasers and enables precise targeting of single cells.

Probing a cell-embedded megadalton protein complex by DNP-supported solid-state NMR   pp649 - 652
Mohammed Kaplan, Abhishek Cukkemane, Gydo C P van Zundert, Siddarth Narasimhan, Mark Daniëls et al.
doi:10.1038/nmeth.3406
Dynamic nuclear polarization-based solid-state nuclear magnetic resonance spectroscopyis applied to study the structure of a large bacterial membrane protein complex in its cellular environment.

Traction microscopy to identify force modulation in subresolution adhesions   pp653 - 656
Sangyoon J Han, Youbean Oak, Alex Groisman and Gaudenz Danuser
doi:10.1038/nmeth.3430
An analytical method, with accompanying software, is described for improved fidelity in traction force microscopy and is used to measure forces at emerging focal adhesions at high resolution.

Dexterous robotic manipulation of alert adult Drosophila for high-content experimentation   pp657 - 660
Joan Savall, Eric Tatt Wei Ho, Cheng Huang, Jessica R Maxey and Mark J Schnitzer
doi:10.1038/nmeth.3410
A robotic system is described that uses machine vision guidance to pick, manipulate, inspect and dissect individual flies, enabling large-scale and automated approaches to the analysis of morphology, behavior and neural dynamics.

Application of BRET to monitor ligand binding to GPCRs   pp661 - 663
Leigh A Stoddart, Elizabeth K M Johnstone, Amanda J Wheal, Joëlle Goulding, Matthew B Robers et al.
doi:10.1038/nmeth.3398
Bioluminescence resonance energy transfer, from the substrate of a luciferase fused with a G protein-coupled receptor to a fluorescent dye covalently linked to a receptor ligand, allows the profiling of ligand affinity and binding kinetics.

Articles

Top

Multiplexable, locus-specific targeting of long RNAs with CRISPR-Display   pp664 - 670
David M Shechner, Ezgi Hacisuleyman, Scott T Younger and John L Rinn
doi:10.1038/nmeth.3433
CRISPR-Display is a modular and flexible platform that targets natural or synthetic noncoding RNA domains to specific genomic loci for functional studies and synthetic biology.

See also: News and Views by Lin & Corn

Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture   pp671 - 678
Anca M PaÅŸca, Steven A Sloan, Laura E Clarke, Yuan Tian, Christopher D Makinson et al.
doi:10.1038/nmeth.3415
A method for 3D differentiation of human pluripotent stem cells yields brain cortical spheroids with functional neurons and astrocytes. The spheroids can be sliced for imaging and electrophysiological studies.

Automated determination of fibrillar structures by simultaneous model building and fiber diffraction refinement   pp679 - 684
Wojciech Potrzebowski and Ingemar André
doi:10.1038/nmeth.3399
A computational approach[mdash]including a cross-validation metric[mdash]for automated model building and refinement using X-ray fiber diffraction data is described and applied to solve structures of protein fibers.

A microfluidic device for label-free, physical capture of circulating tumor cell clusters   pp685 - 691
A Fatih Sarioglu, Nicola Aceto, Nikola Kojic, Maria C Donaldson, Mahnaz Zeinali et al.
doi:10.1038/nmeth.3404
The Cluster-Chip provides highly efficient and gentle capture of circulating tumor cell clusters from milliliters of unprocessed whole blood, making it possible to study how these clusters contribute to metastasis.

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Corrigenda

Top

Corrigendum: Fast native-SAD phasing for routine macromolecular structure determination   p692
Tobias Weinert, Vincent Olieric, Sandro Waltersperger, Ezequiel Panepucci, Lirong Chen et al.
doi:10.1038/nmeth0715-692a

Corrigendum: Simultaneous all-optical manipulation and recording of neural circuit activity with cellular resolution in vivo   p692
Adam M Packer, Lloyd E Russell, Henry W P Dalgleish and Michael Häusser
doi:10.1038/nmeth0715-692b

Corrigendum: Fixation-resistant photoactivatable fluorescent proteins for CLEM   p692
Maria G Paez-Segala, Mei G Sun, Gleb Shtengel, Sarada Viswanathan, Michelle A Baird et al.
doi:10.1038/nmeth0715-692c

Corrigendum: Accurate macromolecular structures using minimal measurements from X-ray free-electron lasers   p692
Johan Hattne, Nathaniel Echols, Rosalie Tran, Jan Kern, Richard J Gildea et al.
doi:10.1038/nmeth0715-692d

Top
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