Bending the genome.

Abstract:

:

journal_name

Nat Methods

journal_title

Nature methods

authors

Rusk N

doi

10.1038/s41592-018-0270-1

subject

pub_date

2019-01-01 00:00:00

pages

18

issue

1

eissn

1548-7091

issn

1548-7105

pii

10.1038/s41592-018-0270-1

journal_volume

16

pub_type

杂志文章
  • High-resolution mass spectrometry of small molecules bound to membrane proteins.

    abstract::Small molecules are known to stabilize membrane proteins and to modulate their function and oligomeric state, but such interactions are often hard to precisely define. Here we develop and apply a high-resolution, Orbitrap mass spectrometry-based method for analyzing intact membrane protein-ligand complexes. Using this...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3771

    authors: Gault J,Donlan JA,Liko I,Hopper JT,Gupta K,Housden NG,Struwe WB,Marty MT,Mize T,Bechara C,Zhu Y,Wu B,Kleanthous C,Belov M,Damoc E,Makarov A,Robinson CV

    更新日期:2016-04-01 00:00:00

  • Dynamic characterization of growth and gene expression using high-throughput automated flow cytometry.

    abstract::Cells adjust to changes in environmental conditions using complex regulatory programs. These cellular programs are the result of an intricate interplay between gene expression, cellular growth and protein degradation. Technologies that enable simultaneous and time-resolved measurements of these variables are necessary...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2879

    authors: Zuleta IA,Aranda-Díaz A,Li H,El-Samad H

    更新日期:2014-04-01 00:00:00

  • CLARITY for mapping the nervous system.

    abstract::With potential relevance for brain-mapping work, hydrogel-based structures can now be built from within biological tissue to allow subsequent removal of lipids without mechanical disassembly of the tissue. This process creates a tissue-hydrogel hybrid that is physically stable, that preserves fine structure, proteins ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2481

    authors: Chung K,Deisseroth K

    更新日期:2013-06-01 00:00:00

  • Super-resolution imaging in live Caulobacter crescentus cells using photoswitchable EYFP.

    abstract::The commonly used, monomeric EYFP enabled imaging of intracellular protein structures beyond the optical resolution limit ('super-resolution' imaging) in living cells. By combining photoinduced activation of single EYFP fusions and time-lapse imaging, we obtained sub-40 nm resolution images of the filamentous superstr...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1258

    authors: Biteen JS,Thompson MA,Tselentis NK,Bowman GR,Shapiro L,Moerner WE

    更新日期:2008-11-01 00:00:00

  • Identification of differentially methylated cell types in epigenome-wide association studies.

    abstract::An outstanding challenge of epigenome-wide association studies (EWASs) performed in complex tissues is the identification of the specific cell type(s) responsible for the observed differential DNA methylation. Here we present a statistical algorithm called CellDMC ( https://github.com/sjczheng/EpiDISH ), which can ide...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0213-x

    authors: Zheng SC,Breeze CE,Beck S,Teschendorff AE

    更新日期:2018-12-01 00:00:00

  • Stable long-term chronic brain mapping at the single-neuron level.

    abstract::Stable in vivo mapping and modulation of the same neurons and brain circuits over extended periods is critical to both neuroscience and medicine. Current electrical implants offer single-neuron spatiotemporal resolution but are limited by such factors as relative shear motion and chronic immune responses during long-t...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3969

    authors: Fu TM,Hong G,Zhou T,Schuhmann TG,Viveros RD,Lieber CM

    更新日期:2016-10-01 00:00:00

  • Screening for functional circular RNAs using the CRISPR-Cas13 system.

    abstract::Circular RNAs (circRNAs) produced from back-spliced exons are widely expressed, but individual circRNA functions remain poorly understood owing to the lack of adequate methods for distinguishing circRNAs from cognate messenger RNAs with overlapping exons. Here, we report that CRISPR-RfxCas13d can effectively discrimin...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-020-01011-4

    authors: Li S,Li X,Xue W,Zhang L,Yang LZ,Cao SM,Lei YN,Liu CX,Guo SK,Shan L,Wu M,Tao X,Zhang JL,Gao X,Zhang J,Wei J,Li J,Yang L,Chen LL

    更新日期:2021-01-01 00:00:00

  • Comparing the performance of biomedical clustering methods.

    abstract::Identifying groups of similar objects is a popular first step in biomedical data analysis, but it is error-prone and impossible to perform manually. Many computational methods have been developed to tackle this problem. Here we assessed 13 well-known methods using 24 data sets ranging from gene expression to protein d...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3583

    authors: Wiwie C,Baumbach J,Röttger R

    更新日期:2015-11-01 00:00:00

  • A versatile tool for conditional gene expression and knockdown.

    abstract::Drug-inducible systems allowing the control of gene expression in mammalian cells are invaluable tools for genetic research, and could also fulfill essential roles in gene- and cell-based therapy. Currently available systems, however, often have limited in vivo functionality because of leakiness, insufficient levels o...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth846

    authors: Szulc J,Wiznerowicz M,Sauvain MO,Trono D,Aebischer P

    更新日期:2006-02-01 00:00:00

  • Annotating the unannotated.

    abstract::By combining activity-based proteomics and metabolomics, researchers have developed a new systems biology strategy for characterizing enzymes in the context of metabolic networks. ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth0107-8b

    authors: Doerr A

    更新日期:2007-01-01 00:00:00

  • Cell-type-specific signaling networks in heterocellular organoids.

    abstract::Despite the widespread adoption of organoids as biomimetic tissue models, methods to comprehensively analyze cell-type-specific post-translational modification (PTM) signaling networks in organoids are absent. Here, we report multivariate single-cell analysis of such networks in organoids and organoid cocultures. Simu...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-020-0737-8

    authors: Qin X,Sufi J,Vlckova P,Kyriakidou P,Acton SE,Li VSW,Nitz M,Tape CJ

    更新日期:2020-03-01 00:00:00

  • Blotting protein complexes from native gels to electron microscopy grids.

    abstract::We report a simple and generic method for the direct transfer of protein complexes separated by native gel electrophoresis to electron microscopy grids. After transfer, sufficient material remains in the gel for identification and characterization by mass spectrometry. The method should facilitate higher-throughput si...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1840

    authors: Knispel RW,Kofler C,Boicu M,Baumeister W,Nickell S

    更新日期:2012-01-08 00:00:00

  • Fast, high-contrast imaging of animal development with scanned light sheet-based structured-illumination microscopy.

    abstract::Recording light-microscopy images of large, nontransparent specimens, such as developing multicellular organisms, is complicated by decreased contrast resulting from light scattering. Early zebrafish development can be captured by standard light-sheet microscopy, but new imaging strategies are required to obtain high-...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1476

    authors: Keller PJ,Schmidt AD,Santella A,Khairy K,Bao Z,Wittbrodt J,Stelzer EH

    更新日期:2010-08-01 00:00:00

  • Measurement of mechanical tractions exerted by cells in three-dimensional matrices.

    abstract::Quantitative measurements of cell-generated forces have heretofore required that cells be cultured on two-dimensional substrates. We describe a technique to quantitatively measure three-dimensional traction forces exerted by cells fully encapsulated in well-defined elastic hydrogel matrices. Using this approach we mea...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1531

    authors: Legant WR,Miller JS,Blakely BL,Cohen DM,Genin GM,Chen CS

    更新日期:2010-12-01 00:00:00

  • A guide to designing germline-dependent epigenetic inheritance experiments in mammals.

    abstract::Recent work has demonstrated that environmental factors experienced by parents can affect their offspring across multiple generations, and that such transgenerational transmission can depend on the germline. Causal evidence for the involvement of germ cells is rare, however, and the underlying molecular mechanisms rem...

    journal_title:Nature methods

    pub_type: 杂志文章,评审

    doi:10.1038/nmeth.4181

    authors: Bohacek J,Mansuy IM

    更新日期:2017-02-28 00:00:00

  • FRETting for a more detailed interactome.

    abstract::A quantitative high-throughput FRET-based method of screening fluorescent protein fusion libraries brings the promise of more detailed interactome maps. ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth0207-112b

    authors: Kaganman I

    更新日期:2007-02-01 00:00:00

  • Development and applications of single-cell transcriptome analysis.

    abstract::Dissecting the relationship between genotype and phenotype is one of the central goals in developmental biology and medicine. Transcriptome analysis is a powerful strategy to connect genotype to phenotype of a cell. Here we review the history, progress, potential applications and future developments of single-cell tra...

    journal_title:Nature methods

    pub_type: 历史文章,杂志文章,评审

    doi:10.1038/nmeth.1557

    authors: Tang F,Lao K,Surani MA

    更新日期:2011-04-01 00:00:00

  • High-throughput genetic interaction mapping in the fission yeast Schizosaccharomyces pombe.

    abstract::Epistasis analysis, which reports on the extent to which the function of one gene depends on the presence of a second, is a powerful tool for studying the functional organization of the cell. Systematic genome-wide studies of epistasis, however, have been limited, with the majority of data being collected in the buddi...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth1098

    authors: Roguev A,Wiren M,Weissman JS,Krogan NJ

    更新日期:2007-10-01 00:00:00

  • Bright monomeric red fluorescent protein with an extended fluorescence lifetime.

    abstract::Fluorescent proteins have become extremely popular tools for in vivo imaging and especially for the study of localization, motility and interaction of proteins in living cells. Here we report TagRFP, a monomeric red fluorescent protein, which is characterized by high brightness, complete chromophore maturation, prolon...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth1062

    authors: Merzlyak EM,Goedhart J,Shcherbo D,Bulina ME,Shcheglov AS,Fradkov AF,Gaintzeva A,Lukyanov KA,Lukyanov S,Gadella TW,Chudakov DM

    更新日期:2007-07-01 00:00:00

  • Quantifying domain-ligand affinities and specificities by high-throughput holdup assay.

    abstract::Many protein interactions are mediated by small linear motifs interacting specifically with defined families of globular domains. Quantifying the specificity of a motif requires measuring and comparing its binding affinities to all its putative target domains. To this end, we developed the high-throughput holdup assay...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3438

    authors: Vincentelli R,Luck K,Poirson J,Polanowska J,Abdat J,Blémont M,Turchetto J,Iv F,Ricquier K,Straub ML,Forster A,Cassonnet P,Borg JP,Jacob Y,Masson M,Nominé Y,Reboul J,Wolff N,Charbonnier S,Travé G

    更新日期:2015-08-01 00:00:00

  • Single-cell systems biology by super-resolution imaging and combinatorial labeling.

    abstract::Fluorescence microscopy is a powerful quantitative tool for exploring regulatory networks in single cells. However, the number of molecular species that can be measured simultaneously is limited by the spectral overlap between fluorophores. Here we demonstrate a simple but general strategy to drastically increase the ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2069

    authors: Lubeck E,Cai L

    更新日期:2012-06-03 00:00:00

  • Streaming fragment assignment for real-time analysis of sequencing experiments.

    abstract::We present eXpress, a software package for efficient probabilistic assignment of ambiguously mapping sequenced fragments. eXpress uses a streaming algorithm with linear run time and constant memory use. It can determine abundances of sequenced molecules in real time and can be applied to ChIP-seq, metagenomics and oth...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2251

    authors: Roberts A,Pachter L

    更新日期:2013-01-01 00:00:00

  • Marker-independent identification of glioma-initiating cells.

    abstract::Tumor-initiating cells with stem cell properties are believed to sustain the growth of gliomas, but proposed markers such as CD133 cannot be used to identify these cells with sufficient specificity. We report an alternative isolation method purely based on phenotypic qualities of glioma-initiating cells (GICs), avoidi...

    journal_title:Nature methods

    pub_type: 杂志文章,收录出版

    doi:10.1038/nmeth.1430

    authors: Clément V,Marino D,Cudalbu C,Hamou MF,Mlynarik V,de Tribolet N,Dietrich PY,Gruetter R,Hegi ME,Radovanovic I

    更新日期:2010-03-01 00:00:00

  • Terminal exon characterization with TECtool reveals an abundance of cell-specific isoforms.

    abstract::Sequencing of RNA 3' ends has uncovered numerous sites that do not correspond to the termination sites of known transcripts. Through their 3' untranslated regions, protein-coding RNAs interact with RNA-binding proteins and microRNAs, which regulate many properties, including RNA stability and subcellular localization....

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0114-z

    authors: Gruber AJ,Gypas F,Riba A,Schmidt R,Zavolan M

    更新日期:2018-10-01 00:00:00

  • Highly multiplexed simultaneous detection of RNAs and proteins in single cells.

    abstract::To enable the detection of expression signatures specific to individual cells, we developed PLAYR (proximity ligation assay for RNA), a method for highly multiplexed transcript quantification by flow and mass cytometry that is compatible with standard antibody staining. When used with mass cytometry, PLAYR allowed for...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3742

    authors: Frei AP,Bava FA,Zunder ER,Hsieh EW,Chen SY,Nolan GP,Gherardini PF

    更新日期:2016-03-01 00:00:00

  • Monitoring multiple distances within a single molecule using switchable FRET.

    abstract::The analysis of structure and dynamics of biomolecules is important for understanding their function. Toward this aim, we introduce a method called 'switchable FRET', which combines single-molecule fluorescence resonance energy transfer (FRET) with reversible photoswitching of fluorophores. Typically, single-molecule ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.1502

    authors: Uphoff S,Holden SJ,Le Reste L,Periz J,van de Linde S,Heilemann M,Kapanidis AN

    更新日期:2010-10-01 00:00:00

  • High-performance probes for light and electron microscopy.

    abstract::We describe an engineered family of highly antigenic molecules based on GFP-like fluorescent proteins. These molecules contain numerous copies of peptide epitopes and simultaneously bind IgG antibodies at each location. These 'spaghetti monster' fluorescent proteins (smFPs) distributed well in neurons, notably into sm...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3365

    authors: Viswanathan S,Williams ME,Bloss EB,Stasevich TJ,Speer CM,Nern A,Pfeiffer BD,Hooks BM,Li WP,English BP,Tian T,Henry GL,Macklin JJ,Patel R,Gerfen CR,Zhuang X,Wang Y,Rubin GM,Looger LL

    更新日期:2015-06-01 00:00:00

  • Nanoscale imaging of RNA with expansion microscopy.

    abstract::The ability to image RNA identity and location with nanoscale precision in intact tissues is of great interest for defining cell types and states in normal and pathological biological settings. Here, we present a strategy for expansion microscopy of RNA. We developed a small-molecule linker that enables RNA to be cova...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3899

    authors: Chen F,Wassie AT,Cote AJ,Sinha A,Alon S,Asano S,Daugharthy ER,Chang JB,Marblestone A,Church GM,Raj A,Boyden ES

    更新日期:2016-08-01 00:00:00

  • scGen predicts single-cell perturbation responses.

    abstract::Accurately modeling cellular response to perturbations is a central goal of computational biology. While such modeling has been based on statistical, mechanistic and machine learning models in specific settings, no generalization of predictions to phenomena absent from training data (out-of-sample) has yet been demons...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-019-0494-8

    authors: Lotfollahi M,Wolf FA,Theis FJ

    更新日期:2019-08-01 00:00:00

  • Neutron-encoded mass signatures for multiplexed proteome quantification.

    abstract::We describe a protein quantification method called neutron encoding that exploits the subtle mass differences caused by nuclear binding energy variation in stable isotopes. These mass differences are synthetically encoded into amino acids and incorporated into yeast and mouse proteins via metabolic labeling. Mass spec...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.2378

    authors: Hebert AS,Merrill AE,Bailey DJ,Still AJ,Westphall MS,Strieter ER,Pagliarini DJ,Coon JJ

    更新日期:2013-04-01 00:00:00