Purification and Structural Analysis of Desmoplakin.

Abstract:

:Desmoplakin (DP) is an obligate component of desmosomes, where it links the desmosomal cadherin/plakoglobin/plakophilin assembly to intermediate filaments. DP contains a large amino-terminal domain (DPNT) that binds to the cadherin/plakoglobin/plakophilin complex, a central coiled-coil domain that dimerizes the molecule, and a C-terminal domain (DPCT) that binds to intermediate filaments. DPNT contains a plakin domain, comprising a set of spectrin-like repeats. DPCT contains three plakin repeat domains, each formed by 4.5 repeats of a sequence motif known as a plakin repeat that bind to intermediate filaments. Here, we review purification, biochemical characterization, and structural analysis of the DPNT plakin domain and the DPCT plakin repeat domains.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Choi HJ,Weis WI

doi

10.1016/bs.mie.2015.05.006

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

197-213

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(15)00304-3

journal_volume

569

pub_type

杂志文章
  • 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

  • G protein-coupled receptor internalization assays in the high-content screening format.

    abstract::High-content screening (HCS), a combination of fluorescence microscopic imaging and automated image analysis, has become a frequently applied tool to study test compound effects in cellular disease-modeling systems. This chapter describes the measurement of G protein-coupled receptor (GPCR) internalization in the HCS ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(06)14008-2

    authors: Haasen D,Schnapp A,Valler MJ,Heilker R

    更新日期:2006-01-01 00:00:00

  • Analysis of Nonsense-Mediated mRNA Decay at the Single-Cell Level Using Two Fluorescent Proteins.

    abstract::Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved mechanism of specific degradation of transcripts with a premature stop codon. NMD eliminates aberrant mRNAs arising from mutations, alternative splicing, and other events in cells. In addition, many normal transcripts undergo NMD. Recent studies demonst...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.02.008

    authors: Gurskaya NG,Pereverzev AP,Staroverov DB,Markina NM,Lukyanov KA

    更新日期:2016-01-01 00:00:00

  • Forward genetic screens to identify circadian rhythm mutants in mice.

    abstract::This article describes the methods and techniques used to produce mutagenized mice to conduct high-throughput forward genetic screens for circadian rhythm mutants in the mouse. In particular, we outline methods to safely prepare and administer the chemical mutagen N-nitroso-N-ethylurea (ENU) to mice. We also discuss t...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)93007-3

    authors: Siepka SM,Takahashi JS

    更新日期:2005-01-01 00:00:00

  • Methods for measuring HMGB1 release during immunogenic cell death.

    abstract::The exodus of the alarmin high mobility group box 1 (HMGB1) from the nucleus constitutes a crucial cellular danger signal and manifests as a sequential process in which HMGB1 first exits the nucleus into the cytoplasm and then is secreted or passively released through the permeabilized plasma membrane. Extracellular H...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2019.05.001

    authors: Zhao L,Liu P,Kepp O,Kroemer G

    更新日期:2019-01-01 00:00:00

  • GEF and glucosylation assays on liposome-bound Rac.

    abstract::Rac binds tightly to lipid membranes through a lipid modification. The influence of the lipid membrane environment on the multiple interactions of Rac has not been well documented. In this chapter, we detail a method to prepare geranyl-geranylated Rac bound to liposomes of defined composition. With this method, one ca...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(06)06006-X

    authors: Mesmin B,Antonny B

    更新日期:2006-01-01 00:00:00

  • Development of accurate force fields for the simulation of biomineralization.

    abstract::The existence of an accurate force field (FF) model that reproduces the free-energy landscape is a key prerequisite for the simulation of biomineralization. Here, the stages in the development of such a model are discussed including the quality of the water model, the thermodynamics of polymorphism, and the free energ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/B978-0-12-416617-2.00001-1

    authors: Raiteri P,Demichelis R,Gale JD

    更新日期:2013-01-01 00:00:00

  • Droplet confinement and fluorescence measurement of single molecules.

    abstract::We describe a method for molecular confinement and single-fluorophore sensitive measurement in aqueous nanodroplets in oil. The sequestration of individual molecules in droplets has become a useful tool in genomics and molecular evolution. Similarly, the use of single fluorophores, or pairs of fluorophores, to study b...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(10)72015-2

    authors: Goldner LS,Jofre AM,Tang J

    更新日期:2010-01-01 00:00:00

  • Aminocoumarins mutasynthesis, chemoenzymatic synthesis, and metabolic engineering.

    abstract::The aminocoumarin antibiotics novobiocin, clorobiocin and coumermycin A(1) are formed by different Streptomyces strains and are potent inhibitors of bacterial gyrase. Their biosynthetic gene clusters have been analyzed in detail by genetic and biochemical investigations. Heterologous expression of these gene clusters ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(09)04618-7

    authors: Heide L

    更新日期:2009-01-01 00:00:00

  • Rapid purification of native dynamin I and colorimetric GTPase assay.

    abstract::Dynamin I is a large GTPase enzyme required in membrane constriction and fission during multiple forms of endocytosis. The first method described here is for the rapid purification of native dynamin from peripheral membrane extracts of sheep brain using ammonium sulfate precipitation and affinity purification on recom...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)04049-8

    authors: Quan A,Robinson PJ

    更新日期:2005-01-01 00:00:00

  • TM4 microarray software suite.

    abstract::Powerful specialized software is essential for managing, quantifying, and ultimately deriving scientific insight from results of a microarray experiment. We have developed a suite of software applications, known as TM4, to support such gene expression studies. The suite consists of open-source tools for data managemen...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(06)11009-5

    authors: Saeed AI,Bhagabati NK,Braisted JC,Liang W,Sharov V,Howe EA,Li J,Thiagarajan M,White JA,Quackenbush J

    更新日期:2006-01-01 00:00:00

  • Transgenic models to understand hypoxia-inducible factor function.

    abstract::The hypoxia-inducible factor (HIF) is a heterodimeric basic helix-loop-helix (bHLH) transcription factor that controls the mammalian cellular transcriptional response to low oxygen tension by up-regulating genes including glycolytic enzymes and angiogenic factors, such as the vascular endothelial growth factor (VEGF)....

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(07)35005-2

    authors: Doedens A,Johnson RS

    更新日期:2007-01-01 00:00:00

  • Discovery of ligands for beta gamma subunits from phage-displayed peptide libraries.

    abstract::We have described a method using polyvalent peptide display on filamentous phage that can be used to identify ligands that bind to G protein beta gamma subunits. Also described is how to construct phage that have known beta gamma binding sequences fused to the coat protein to allow a competition analysis to be perform...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/s0076-6879(02)44740-4

    authors: Smrcka AV,Scott JK

    更新日期:2002-01-01 00:00:00

  • Mod-seq: A High-Throughput Method for Probing RNA Secondary Structure.

    abstract::It has become increasingly clear that large RNA molecules, especially long noncoding RNAs, function in almost all gene regulatory processes (Cech & Steitz, 2014). Many large RNAs appear to be structural scaffolds for assembly of important RNA/protein complexes. However, the structures of most large cellular RNA molecu...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2015.01.012

    authors: Lin Y,May GE,Joel McManus C

    更新日期:2015-01-01 00:00:00

  • Epitope tagging and protein surveillance.

    abstract::The epitope tagging approach offers advantages of economy, universality, and precision over the use of antibodies raised directly against a protein of interest. The latter strategy promises a potentially greater diversity of reagents and obviates the need to modify the protein, but it may not yield sufficiently high-a...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/0076-6879(91)94038-e

    authors: Kolodziej PA,Young RA

    更新日期:1991-01-01 00:00:00

  • Reconstituting Plant Secondary Metabolism in Saccharomyces cerevisiae for Production of High-Value Benzylisoquinoline Alkaloids.

    abstract::Benzylisoquinoline alkaloids (BIAs) constitute a diverse class of plant secondary metabolites that includes the opiate analgesics morphine and codeine. Collectively, BIAs exhibit a myriad of pharmacological activities, including antimicrobial, antitussive, antispasmodic, and anticancer properties. Despite 2500 known B...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.02.011

    authors: Pyne ME,Narcross L,Fossati E,Bourgeois L,Burton E,Gold ND,Martin VJ

    更新日期:2016-01-01 00:00:00

  • Imaging single mRNA molecules in yeast.

    abstract::Yeast cells in an isogenic population do not all display the same phenotypes. To study such variation within a population of cells, we need to perform measurements on each individual cell instead of measurements that average out the behavior of a cell over the entire population. Here, we provide the basic concepts and...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(10)70017-3

    authors: Youk H,Raj A,van Oudenaarden A

    更新日期:2010-01-01 00:00:00

  • Identification by MS/MS of disulfides produced by a functional redox transition.

    abstract::Among posttranslational modifications of proteins entailed with signal transduction, the redox transition is today brought to the focus as a major biochemical event accounting for the signaling functions of reactive oxygen species. Thermodynamic and kinetic criteria highlight hydroperoxides and protein disulfides as s...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/S0076-6879(10)73011-1

    authors: Mauri P,Toppo S,De Palma A,Benazzi L,Maiorino M,Ursini F

    更新日期:2010-01-01 00:00:00

  • In vivo expression technology for selection of bacterial genes specifically induced in host tissues.

    abstract::We have developed a genetic system, termed IVET (in vivo expression technology), designed to identify bacterial genes that are induced when a pathogen infects its host. A subset of these induced genes should include those that encode virulence factors, products specifically required for the infection process. The syst...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/0076-6879(94)35164-3

    authors: Slauch JM,Mahan MJ,Mekalanos JJ

    更新日期:1994-01-01 00:00:00

  • Xenopus laevis as Model System to Study DNA Damage Response and Replication Fork Stability.

    abstract::Although many players of the DNA damage response and DNA repair have been identified in several systems their biochemical role is still poorly understood. The use of the Xenopus laevis egg extract cell-free system allowed biochemical dissection of DNA replication and cell cycle events in a complex biological context. ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2017.03.018

    authors: Sannino V,Pezzimenti F,Bertora S,Costanzo V

    更新日期:2017-01-01 00:00:00

  • Reconstitution of cargo-dependent COPII coat assembly on proteoliposomes.

    abstract::The coat protein complex II (COPII) coat is responsible for direct capture of membrane cargo proteins and for the physical deformation of the endoplasmic reticulum (ER) membrane that drives the transport vesicle formation. The use of an in vitro reconstitution system comprising purified components is desirable for stu...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(05)04009-7

    authors: Sato K,Nakano A

    更新日期:2005-01-01 00:00:00

  • BioID Identification of Lamin-Associated Proteins.

    abstract::A- and B-type lamins support the nuclear envelope, contribute to heterochromatin organization, and regulate a myriad of nuclear processes. The mechanisms by which lamins function in different cell types and the mechanisms by which lamin mutations cause over a dozen human diseases (laminopathies) remain unclear. The id...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2015.08.008

    authors: Mehus AA,Anderson RH,Roux KJ

    更新日期:2016-01-01 00:00:00

  • Measuring the activity and structure of functional RNAs inside compartments formed by liquid-liquid phase separation.

    abstract::Liquid-liquid phase separation (LLPS) has been known to drive formation of biomolecular compartments, which can encapsulate RNA and proteins among other cosolutes. Such compartments, which lack a lipid membrane, have been implicated in origins of life scenarios as they can easily uptake and concentrate biomolecules, s...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2020.06.010

    authors: Poudyal RR,Meyer MO,Bevilacqua PC

    更新日期:2021-01-01 00:00:00

  • Pulsed EPR in the Study of Drug Binding in Cytochrome P450 and NOS.

    abstract::Pulsed EPR methods for the study of drug binding to heme-thiolate enzymes such as cytochrome P450 and nitric oxide synthase are discussed. HYSCORE and ENDOR methods to measure (1)H of axial ligands of the heme group are described with illustrations of water serving as the axial ligand in the drug-free enzyme and ligan...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2015.07.005

    authors: Cruce AA,Lockart M,Bowman MK

    更新日期:2015-01-01 00:00:00

  • Kinetic Isotope Effect Analysis of RNA 2'-O-Transphosphorylation.

    abstract::The breaking of RNA strands by 2'-O-transphosphorylation is a ubiquitous reaction in biology, and enzymes that catalyze this reaction play key roles in RNA metabolism. The mechanisms of 2'-O-transphosphorylation in solution are relatively well studied, but complex and can involve different transition states depending ...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2017.07.017

    authors: Harris ME,York DM,Piccirilli JA,Anderson VE

    更新日期:2017-01-01 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

  • Fluorescence line narrowing spectroscopy: a tool for studying proteins.

    abstract::Perhaps the most important contribution of FLN is that it provides an experimental approach to relate physical changes in the protein to predicted dynamical behavior. It is clear that the sample is inhomogeneously broadened in a continuous manner, consistent with the damped motion of proteins. At the same time configu...

    journal_title:Methods in enzymology

    pub_type: 杂志文章,评审

    doi:10.1016/s0076-6879(97)78007-8

    authors: Vanderkooi JM,Angiolillo PJ,Laberge M

    更新日期:1997-01-01 00:00:00

  • Cellular Assays for Evaluating Calcium-Dependent Translocation of cPLA2α to Membrane.

    abstract::The group IVA phospholipase A2, commonly called cytosolic phospholipase A2α (cPLA2α), is a widely expressed enzyme that hydrolyzes membrane phospholipid to produce arachidonic acid and lysophospholipids, which are precursors for a number of bioactive lipid mediators. Arachidonic acid is metabolized through the cycloox...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/bs.mie.2016.09.006

    authors: Yun B,Leslie CC

    更新日期:2017-01-01 00:00:00

  • Viability assays to monitor yeast autophagy.

    abstract::In the yeast Saccharomyces cerevisiae, autophagy contributes to the sustaining of cell viability under starvation conditions, possibly through the supply of amino acids that is generated as a result of the degradation of cytosolic materials. Therefore, cellular viability is one of the best indexes for monitoring the c...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(08)03202-3

    authors: Noda T

    更新日期:2008-01-01 00:00:00

  • Conformational stability of cytochrome C probed by optical spectroscopy.

    abstract::Over the last 50 years cytochrome c has been used as a model system for studying electron transfer and protein folding processes. Recently, convincing evidence has been provided that this protein is also involved in other biological processes such as the apoptosis and α-synuclein aggregation. Numerous lines of evidenc...

    journal_title:Methods in enzymology

    pub_type: 杂志文章

    doi:10.1016/S0076-6879(09)66006-7

    authors: Schweitzer-Stenner R,Hagarman A,Verbaro D,Soffer JB

    更新日期:2009-01-01 00:00:00