High-throughput determination of in vivo DNA sequence preferences for Cas protein binding using Library-ChIP.

Abstract:

:The specificity of CRISPR-Cas systems for nucleic acid targets is determined by a combination of binding and cleavage. Understanding the mechanisms by which Cas proteins specifically select their targets is critical for the development of CRISPR-Cas systems for biotechnology applications. Moreover, the specificity of CRISPR-Cas systems plays an important role in prokaryote evolution due to its role in distinguishing self from nonself. Here, I describe Library-ChIP, a high-throughput method for measuring Cas protein occupancy at many DNA sequence variants in a native prokaryotic host. Library-ChIP can be used to identify the determinants of specificity for Cas protein binding to nucleic acid targets.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Wade JT

doi

10.1016/bs.mie.2018.10.019

subject

Has Abstract

pub_date

2019-01-01 00:00:00

pages

117-132

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(18)30434-8

journal_volume

616

pub_type

杂志文章
  • Genetic Manipulation of Neurofilament Protein Phosphorylation.

    abstract::Neurofilament biology is important to understanding structural properties of axons, such as establishment of axonal diameter by radial growth. In order to study the function of neurofilaments, a series of genetically modified mice have been generated. Here, we describe a brief history of genetic modifications used to ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2015.07.027

    authors: Jones MR,Villalón E,Garcia ML

    更新日期:2016-01-01 00:00:00

  • Real-time cell assays of phospholipase A(2)s using fluorogenic phospholipids.

    abstract::Phospholipase A(2)s (PLA(2)s) are a superfamily of enzymes involved in production of a wide variety of lipid mediators, including arachidonic acid, lysophospholipids, platelet activation factor, and eicosanoids. Fluorescence-based, real-time cellular activity assays for PLA(2)s have been developed as a tool for studyi...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(07)34002-0

    authors: Manna D,Cho W

    更新日期:2007-01-01 00:00:00

  • Monitoring abscopal responses to radiation in mice.

    abstract::Focal radiation therapy has the potential to generate systemic tumor-targeting immune responses so potent as to eradicate anatomically distant, non-irradiated malignant lesions, a phenomenon commonly referred to as "the abscopal response." In cancer patients, bona fide abscopal responses are rare, although the recent ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2019.04.014

    authors: Rodriguez-Ruiz ME,Yamazaki T,Buqué A,Bloy N,Silva VAO,Stafford L,Sato A,Galluzzi L

    更新日期:2020-01-01 00:00:00

  • Nitric oxide production by primary liver cells isolated from amino acid diet-fed rats.

    abstract::Primary mixed liver cells were isolated from rats that had been fed an amino acid (AA) diet in which natural protein was replaced with a defined mixture of pure AAs. Nitric oxide (NO) production from these cells in vitro was monitored using a nitric oxide (NO)-selective fluorescent probe, diaminofluorescein, followed ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)96045-X

    authors: Kotake Y,Kishida H,Nakae D,Floyd RA

    更新日期:2005-01-01 00:00:00

  • The delitto perfetto approach to in vivo site-directed mutagenesis and chromosome rearrangements with synthetic oligonucleotides in yeast.

    abstract::In vivo genome manipulation through site-directed mutagenesis and chromosome rearrangements has been hindered by the difficulty in achieving high frequencies of targeting and the intensive labor required to create altered genomes that do not contain any heterologous sequence. Here we describe our approach, referred to...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)09019-1

    authors: Storici F,Resnick MA

    更新日期:2006-01-01 00:00:00

  • X-ray microdiffraction of biominerals.

    abstract::Biominerals have complex and heterogeneous architectures, hence diffraction experiments with spatial resolutions between 500 nm and 10 μm are extremely useful to characterize them. X-ray beams in this size range are now routinely produced at many synchrotrons. This chapter provides a review of the different hard X-ray...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/B978-0-12-416617-2.00021-7

    authors: Tamura N,Gilbert PU

    更新日期:2013-01-01 00:00:00

  • Sedimentation Equilibrium Analysis of ClpB Self-Association in Diluted and Crowded Solutions.

    abstract::ClpB belongs to the Hsp100 family of ring-forming heat-shock proteins involved in degradation of unfolded/misfolded proteins and in reactivation of protein aggregates. ClpB monomers reversibly associate to form the hexameric molecular chaperone that, together with the DnaK system, has the ability to disaggregate stres...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2015.04.007

    authors: Alfonso C,del Castillo U,Martín I,Muga A,Rivas G

    更新日期:2015-01-01 00:00:00

  • Amphipathic agents for membrane protein study.

    abstract::Membrane proteins (MPs) are insoluble in aqueous media as a result of incompatibility between the hydrophilic property of the solvent molecules and the hydrophobic nature of MP surfaces, normally associated with lipid membranes. Amphipathic compounds are necessary for extraction of these macromolecules from the native...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2014.12.021

    authors: Sadaf A,Cho KH,Byrne B,Chae PS

    更新日期:2015-01-01 00:00:00

  • Chapter 8. Proteomic mapping of the vascular endothelium in vivo for vascular targeting.

    abstract::The mapping and characterization of the vasculature using proteomics offers the opportunity to better understand the steps and molecular mechanisms involved in vascular development, and angiogenesis in particular. Proteomics has many key advantages over genomics, especially in directly determining protein expression. ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(08)03008-5

    authors: Griffin NM,Schnitzer JE

    更新日期:2008-01-01 00:00:00

  • Purification and use of granzyme B.

    abstract::Granzyme B (GrB) is the primary molecular mediator of apoptosis by cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells. It is a unique mammalian aspartic acid-cleaving serine protease. On T cell receptor activation, GrB is released from the CTL cytoplasmic granules by exocytosis, enters the target cells and, ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/s0076-6879(00)22013-2

    authors: Shi L,Yang X,Froelich CJ,Greenberg AH

    更新日期:2000-01-01 00:00:00

  • Investigating Histone Acetylation Stoichiometry and Turnover Rate.

    abstract::Histone acetylation is a dynamic epigenetic modification that functions in the regulation of DNA-templated reactions, such as transcription. This lysine modification is reversibly controlled by histone (lysine) acetyltransferases and deacetylases. Here, we present methods employing isotopic labeling and mass spectrome...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.01.007

    authors: Fan J,Baeza J,Denu JM

    更新日期:2016-01-01 00:00:00

  • Analysis of metabolomic profiling data acquired on GC-MS.

    abstract::Gas chromatography-mass spectrometry (GC-MS) is one of the three most popular analytical platforms for metabolomics and is largely employed for the study of oncometabolism. Large volumes of data are usually generated in a GC-MS experiment, and many analytical steps are required to extract biologically relevant informa...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-801329-8.00016-7

    authors: Koo I,Wei X,Zhang X

    更新日期:2014-01-01 00:00:00

  • Bioluminescence as a classroom tool for scientist volunteers.

    abstract::There is a great need for practicing scientists to volunteer their time and expertise in the K-12th grade science classroom. We have found that bioluminescence is a fun and exciting way to teach basic science concepts and is an excellent tool for the volunteering scientist. We have had very positive reactions from bot...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/s0076-6879(00)05517-8

    authors: Hammer M,Andrade JD

    更新日期:2000-01-01 00:00:00

  • Isolation and identification of eukaryotic initiation factor 4A as a molecular target for the marine natural product Pateamine A.

    abstract::Natural products continue to demonstrate their utility both as therapeutics and as molecular probes for the discovery and mechanistic deconvolution of various cellular processes. However, this utility is dampened by the inherent difficulties involved in isolating and characterizing new bioactive natural products, in o...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(07)31014-8

    authors: Low WK,Dang Y,Schneider-Poetsch T,Shi Z,Choi NS,Rzasa RM,Shea HA,Li S,Park K,Ma G,Romo D,Liu JO

    更新日期:2007-01-01 00:00:00

  • Chapter 9 the duffy antigen receptor for chemokines.

    abstract::The Duffy blood group antigen is a serpentine protein with seven transmembrane domains that is not coupled to G-proteins or other known intracellular effectors. In addition to erythrocytes, it is also expressed in endothelial cells and neurons. In recent years the Duffy antigen has received much attention because of i...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(09)05409-3

    authors: Rot A,Horuk R

    更新日期:2009-01-01 00:00:00

  • Monitoring gasdermin pore formation in vitro.

    abstract::The gasdermin (GSDM) family consists of gasdermin A (GSDMA), B (GSDMB), C (GSDMC), D (GSDMD), E or DNFA5 (GSDME), and DFNB59 in human. Expressed in the skin, gastrointestinal tract, and various immune cells, GSDMs mediate homeostasis and inflammation upon activation by caspases and unknown proteases. In particular, GS...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2019.04.024

    authors: Xia S,Ruan J,Wu H

    更新日期:2019-01-01 00:00:00

  • Gene expression omnibus: microarray data storage, submission, retrieval, and analysis.

    abstract::The Gene Expression Omnibus (GEO) repository at the National Center for Biotechnology Information archives and freely distributes high-throughput molecular abundance data, predominantly gene expression data generated by DNA microarray technology. The database has a flexible design that can handle diverse styles of bot...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(06)11019-8

    authors: Barrett T,Edgar R

    更新日期:2006-01-01 00:00:00

  • The role of EFA6, exchange factor for Arf6, for tight junction assembly, functions, and interaction with the actin cytoskeleton.

    abstract::In polarized epithelial cells, the tight junction has been ascribed several functions including the regulation of the paracellular permeability, an impediment to the diffusion of molecules between the apical and basolateral domains, a site of delivery of transport vesicles for basolateral proteins, and a scaffold for ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)04029-2

    authors: Luton F

    更新日期:2005-01-01 00:00:00

  • Mammalian photoentrainment: results, methods, and approaches.

    abstract::Research on circadian biology over the past decade has paid increasing attention to the photoreceptor mechanisms that align the molecular clock to the 24-h light/dark cycle, and some of the results to emerge are surprising. For example, the rods and cones within the mammalian eye are not required for entrainment. A po...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(05)93037-1

    authors: Peirson SN,Thompson S,Hankins MW,Foster RG

    更新日期:2005-01-01 00:00:00

  • Assays of nuclear localization of R7/Gbeta5 complexes.

    abstract::Heterodimeric complexes between individual members of the R7 subfamily of regulators of G-protein signaling proteins and the Gbeta5 isoform of the heterotrimeric G-protein beta subunit family are strongly expressed in the cell nucleus in neurons and brain, as well as in the cytoplasm and plasma membrane. Native and re...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(04)90014-6

    authors: Simonds WF,Woodard GE,Zhang JH

    更新日期:2004-01-01 00:00:00

  • Recent Advances in Development of Genetically Encoded Fluorescent Sensors.

    abstract::Genetically encoded fluorescent sensors are essential tools in modern biological research, and recent advances in fluorescent proteins (FPs) have expanded the scope of sensor design and implementation. In this review we compare different sensor platforms, including Förster resonance energy transfer (FRET) sensors, flu...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/bs.mie.2017.01.019

    authors: Sanford L,Palmer A

    更新日期:2017-01-01 00:00:00

  • Determining cellular role of G alpha 12.

    abstract::Using the expression strategies described here, we have demonstrated a model system whereby the sequential signaling events involved in cell proliferation and subsequent transformation regulated by G alpha 12 can be investigated. The model system presented here can also be used to study the temporal interrelationships...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/s0076-6879(02)44722-2

    authors: Dermott JM,Dhanasekaran N

    更新日期:2002-01-01 00:00:00

  • Testing pulse detection algorithms with simulations of episodically pulsatile substrate, metabolite, or hormone release.

    abstract::Mathematical computer-assisted simulations of episodic hormone, substrate, or metabolite release can be accomplished using explicit algebra and high-speed microprocessors. Such simulations are useful to describe the behavior of single or multiple pulse generators, as well as the expected output of these systems. Simul...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/s0076-6879(94)40056-3

    authors: Veldhuis JD,Johnson ML

    更新日期:1994-01-01 00:00:00

  • Coupling antibody to cyanogen bromide-activated sepharose.

    abstract::Antibodies will be immobilized on a cyanogen bromide-activated Sepharose for subsequent use in pull-down assays or immunoaffinity purification. ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-420119-4.00003-3

    authors: Kavran JM,Leahy DJ

    更新日期:2014-01-01 00:00:00

  • Isolation and quantitation of adiponectin higher order complexes.

    abstract::Adiponectin is a circulating bioactive hormone secreted by adipocytes as oligomers ranging in size from 90 kDa trimers and 180 kDa hexamers to larger high molecular weight oligomers that may reach 18- or 36-mers in size. While total circulating adiponectin levels correlate well with metabolic health, it is the relativ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-411619-1.00013-6

    authors: Rutkowski JM,Scherer PE

    更新日期:2014-01-01 00:00:00

  • Predicting G-protein-coupled receptors families using different physiochemical properties and pseudo amino acid composition.

    abstract::G-protein-coupled receptors (GPCRs) initiate signaling pathways via trimetric guanine nucleotide-binding proteins. GPCRs are classified based on their ligand-binding properties and molecular phylogenetic analyses. Nonetheless, these later analyses are in most case dependent on multiple sequence alignments, themselves ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-407865-9.00004-2

    authors: Rehman ZU,Mirza MT,Khan A,Xhaard H

    更新日期:2013-01-01 00:00:00

  • Functional Characterization of Histone Chaperones Using SNAP-Tag-Based Imaging to Assess De Novo Histone Deposition.

    abstract::Histone chaperones-key actors in the dynamic organization of chromatin-interact with the various histone variants to ensure their transfer in and out of chromatin. In vitro chromatin assembly assays and isolation of protein complexes using tagged histone variants provided first clues concerning their binding specifici...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.04.004

    authors: Clément C,Vassias I,Ray-Gallet D,Almouzni G

    更新日期:2016-01-01 00:00:00

  • Computational methods for high-throughput comparative analyses of natural microbial communities.

    abstract::One of the most widely employed methods in metagenomics is the amplification and sequencing of the highly conserved ribosomal RNA (rRNA) genes from organisms in complex microbial communities. rRNA surveys, typically using the 16S rRNA gene for prokaryotic identification, provide information about the total diversity a...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-407863-5.00018-6

    authors: Preheim SP,Perrotta AR,Friedman J,Smilie C,Brito I,Smith MB,Alm E

    更新日期:2013-01-01 00:00:00

  • LC-MS-MS analysis of neutral eicosanoids.

    abstract::The neutral arachidonic acid derivatives N-arachidonoyl ethanolamine (anandamide or AEA), and 2-arachidonoylglycerol (2-AG) have been identified as endogenous ligands for the cannabinoid receptors. Additionally, these compounds have been identified as substrates of the second isoform of the cyclooxygenase enzyme (COX-...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(07)33005-X

    authors: Kingsley PJ,Marnett LJ

    更新日期:2007-01-01 00:00:00

  • Membrane protein expression and analysis in yeast.

    abstract::This protocol describes the expression and analysis of membrane proteins produced in yeast, as illustrated with Yarrowia lipolytica and Pichia pastoris. Step by step, we explain how to generate a yeast strain expressing the membrane protein of interest, how to prepare a membrane protein sample from yeast, and how to a...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2014.12.010

    authors: Claes K,Guerfal M,Callewaert N

    更新日期:2015-01-01 00:00:00