Tuesday, May 31, 2016

Nature Methods Contents: June 2016 Volume 13 pp 459 - 535

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Nature Methods

TABLE OF CONTENTS

June 2016 Volume 13, Issue 6

In This Issue
Editorial
This Month
Research Highlights
Technology Feature
News and Views
Brief Communications
Articles
Corrigendum
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In This Issue

Top

In This Issue   

Editorial

Top

Mark the methods in human embryo research   p459
doi:10.1038/nmeth.3896
Research on human embryos depends on precious samples that are inherently variable. Rigorous methods reporting should be the goal of published papers in the field.

This Month

Top

The Author File: Richard D. Cummings   p461
Vivien Marx
doi:10.1038/nmeth.3874
A bleaching method for glycobiology and some impromptu fund-raising at the piano.

Points of View: Binning high-resolution data   p463
Martin Krzywinski
doi:10.1038/nmeth.3873
Limitations in print resolution and visual acuity impose limits on data density and detail.

Research Highlights

Top

RNA structure from sequence
An approach taken from protein structure prediction makes it possible to computationally identify secondary and tertiary contacts in RNA.

PCR for cellular forces
A 'mechanically induced catalytic amplification reaction' reads out receptor-mediated forces in cells.

Of TRIBE and RNA tagging
Genetic approaches profile RNA-protein interactions.

Sensing calcium in red
Red-shifted calcium sensors are advantageous for deep-tissue imaging, dual-color applications and combining with optogenetic tools.

Retraining an editor as a mapmaker
A sequence-specific labeling system based on CRISPR/Cas9 enables simultaneous imaging of multiple chromosomal sites in live cells.

Tunable light-sheet microscopy
Tiling light-sheet microscopy improves live cell imaging of multicellular organisms.

Methods in Brief

Improved RNA interactomes | Nanopores for multiplexed protein sensing | Variants that change transcription factor binding | Open-source software for structured illumination

Tools in Brief

Tracking β-galactosidase activity in vivo | Mapping nanopore sequence reads | Optimized tracing of neural circuits | Fast RNA-seq quantification

Methods
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Technology Feature

Top

PCR: the price of infidelity   pp475 - 479
Vivien Marx
doi:10.1038/nmeth.3868
Infidelity is painful in life and in the lab. The former is better left to other publications; the latter is best not ignored, especially in the context of PCR-based DNA amplification.

News and Views

Top

Expansion microscopy passes its first test   pp481 - 482
Hylkje Geertsema and Helge Ewers
doi:10.1038/nmeth.3872
Simplification of expansion microscopy makes it broadly accessible and compatible with other approaches.

See also: Brief Communication by Chozinski et al.

Redesigning CLIP for efficiency, accuracy and speed   pp482 - 483
Georges Martin and Mihaela Zavolan
doi:10.1038/nmeth.3870
Two new approaches for target profiling of RNA-binding proteins require less cell material, avoid radioactive reagents and give more accurate data in a shorter time compared to previous methods.

See also: Brief Communication by Zarnegar et al. | Article by Van Nostrand et al.

Brief Communications

Top

Expansion microscopy with conventional antibodies and fluorescent proteins   pp485 - 488
Tyler J Chozinski, Aaron R Halpern, Haruhisa Okawa, Hyeon-Jin Kim, Grant J Tremel et al.
doi:10.1038/nmeth.3833
Improved sample preparation methods allow super-resolution imaging by expansion microscopy using endogenous fluorescent protein signal and conventional fluorescently labeled antibodies.

See also: News and Views by Geertsema & Ewers

irCLIP platform for efficient characterization of protein-RNA interactions   pp489 - 492
Brian J Zarnegar, Ryan A Flynn, Ying Shen, Brian T Do, Howard Y Chang et al.
doi:10.1038/nmeth.3840
The use of a biotinylated adaptor conjugated to an infrared dye allows rapid, sensitive, and quantitative analysis of protein-RNA interactions.

See also: News and Views by Martin & Zavolan

Automated mapping of phenotype space with single-cell data   pp493 - 496
Nikolay Samusik, Zinaida Good, Matthew H Spitzer, Kara L Davis and Garry P Nolan
doi:10.1038/nmeth.3863
X-shift software allows automated mapping of phenotypic space from large mass cytometry data sets. X-shift and the new representation algorithm Divisive Marker Tree provide a rapid, deterministic approach to navigating complex cellular systems.

An unbiased metric of antiproliferative drug effect in vitro   pp497 - 500
Leonard A Harris, Peter L Frick, Shawn P Garbett, Keisha N Hardeman, B Bishal Paudel et al.
doi:10.1038/nmeth.3852
Conventional metrics for assessing antiproliferative drug effect have time-dependent biases that may skew results. The drug-induced proliferation rate can be used as an alternative metric for accurate and reproducible assessment of drug performance.

siFLIM: single-image frequency-domain FLIM provides fast and photon-efficient lifetime data   pp501 - 504
Marcel Raspe, Katarzyna M Kedziora, Bram van den Broek, Qiaole Zhao, Sander de Jong et al.
doi:10.1038/nmeth.3836
Single-image fluorescence lifetime imaging microscopy (siFLIM) uses a modulated-FLIM camera to record lifetimes in a single snapshot, allowing for photon-efficient and quantitative lifetime imaging of rapid cellular processes.

Monovar: single-nucleotide variant detection in single cells   pp505 - 507
Hamim Zafar, Yong Wang, Luay Nakhleh, Nicholas Navin and Ken Chen
doi:10.1038/nmeth.3835
Monovar efficiently detects single-nucleotide variants in single-cell DNA sequence data with high sensitivity and specificity.

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Articles

Top

Robust transcriptome-wide discovery of RNA-binding protein binding sites with enhanced CLIP (eCLIP)   pp508 - 514
Eric L Van Nostrand, Gabriel A Pratt, Alexander A Shishkin, Chelsea Gelboin-Burkhart, Mark Y Fang et al.
doi:10.1038/nmeth.3810
Enhanced CLIP yields complex libraries of RNA components of ribonucleoprotein complexes and maintains single-nucleotide resolution of binding sites. eCLIP enables large scale profiling, as demonstrated with the binding profiles of 73 RBPs in two human cancer cell lines.

See also: News and Views by Martin & Zavolan

Automated structure modeling of large protein assemblies using crosslinks as distance restraints   pp515 - 520
Mathias Ferber, Jan Kosinski, Alessandro Ori, Umar J Rashid, María Moreno-Morcillo et al.
doi:10.1038/nmeth.3838
A method and accompanying software tool enables automated modeling of large macromolecular complexes using experimental crosslinking mass spectrometry data as distance restraints, as demonstrated for the 17-subunit yeast RNA polymerase III complex.

Growth rate inhibition metrics correct for confounders in measuring sensitivity to cancer drugs   pp521 - 527
Marc Hafner, Mario Niepel, Mirra Chung and Peter K Sorger
doi:10.1038/nmeth.3853
Growth inhibition metrics allow for robust measurement of drug efficacy independent of variables such as cell growth rate, seeding density, and growth medium; they are a practical alternative to metrics such as IC50 and offer enhanced reproducibility.

Oxidative release of natural glycans for functional glycomics   pp528 - 534
Xuezheng Song, Hong Ju, Yi Lasanajak, Matthew R Kudelka, David F Smith et al.
doi:10.1038/nmeth.3861
Treating glycoproteins with household bleach releases N- and O-glycans for further structural probing. Bleach treatment of glycosphingolipids releases glycan nitriles.

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Corrigendum

Top

Corrigendum: Analyzing outliers: influential or nuisance?   p535
Naomi Altman and Martin Krzywinski
doi:10.1038/nmeth0616-535

Top
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