A four-step, inexpensive protocol for large-scale purification of goat uterine estrogen receptor.

Abstract:

:A relatively inexpensive yet highly efficient and extremely rapid procedure has been developed for the isolation and purification of estrogen receptor from the goat uterine cytosol. Greater than 1 mg of purified receptor protein could be obtained from 75 g of uterine tissue within a period of < 24 h, following this protocol. The procedure does not require the use of an ultracentrifuge, a cold room, or a column chromatography setup. The entire isolation procedure, which involves adsorption to and selective elution from different chromatography matrices, is carried out at the laboratory bench using beakers kept in an ice bath. Antibodies raised against this receptor cross-react with the goat uterine estrogen receptor activation factor, a DNA binding protein having no capacity to bind estradiol but which dimerizes with the nonactivated estrogen receptor, an estrogen receptor incapable of binding to DNA on its own.

journal_name

Protein Expr Purif

authors

Zafar A,Thampan RV

doi

10.1006/prep.1993.1070

subject

Has Abstract

pub_date

1993-12-01 00:00:00

pages

534-8

issue

6

eissn

1046-5928

issn

1096-0279

pii

S1046-5928(83)71070-3

journal_volume

4

pub_type

杂志文章
  • EcoliOverExpressionDB: a database of recombinant protein overexpression in E. coli.

    abstract:UNLABELLED:Recombinant protein production is a significant biotechnological process as it allows researchers to produce a specific protein in desired quantities. Escherichia coli (E. coli) is the most popular heterologous expression host for the production of recombinant proteins due to its advantages such as low cost,...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2013.11.014

    authors: Habibi N,Samian MR,Hashim SZ,Norouzi A

    更新日期:2014-03-01 00:00:00

  • High yield expression and purification of isotopically labelled human endothelin-1 for use in NMR studies.

    abstract::Human endothelin-1 (ET-1) is a potent vasocontractile 21-residue peptide hormone with significant pharmacological importance. An efficient and straightforward expression strategy that enables cost-effective incorporation of stable isotopes is not available thus far. In this report, we describe a cost-effective express...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2006.01.022

    authors: Mac TT,Beyermann M,Pires JR,Schmieder P,Oschkinat H

    更新日期:2006-08-01 00:00:00

  • Development of stable isotope and selenomethionine labeling methods for proteins expressed in Pseudomonas fluorescens.

    abstract::Pseudomonas fluorescens is a robust protein expression system that is very well suited for high throughput protein expression for structural genomics studies. Since NMR spectroscopy and X-ray crystallography are both used by various investigators in structure elucidation studies, the availability of target proteins la...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2008.12.012

    authors: Madduri K,Badger M,Li ZS,Xu X,Thornburgh S,Evans S,Dhadialla TS

    更新日期:2009-05-01 00:00:00

  • A new method for the purification of bioactive insulin-like growth factor-binding protein-3.

    abstract::We present a novel efficient procedure for high level purification of human IGFBP-3. Insulin-like growth factor-binding proteins (IGFBPs) are key regulators of insulin-like growth factor mediated signal transduction and thereby can profoundly influence cellular phenotypes. Certain IGFBPs, including IGFBP-3, have also ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2010.02.005

    authors: Pircher H,Matscheski A,Laich A,Hermann M,Moser B,Viertler HP,Micutkova L,Lindner H,Sarg B,Zwerschke W,Jansen-Dürr P

    更新日期:2010-06-01 00:00:00

  • Expression and purification of a putative H-NS nucleoid-associated protein from the phytopathogen Xylella fastidiosa.

    abstract::The H-NS protein is one of the major constituents of the nucleoid structure that has been implicated in the DNA packaging and in the global regulation of gene expression. The study of this transcriptional regulator is an effort to fight Xylella fastidiosa, a citrus pathogen responsible for a range of economically impo...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/S1046-5928(03)00193-1

    authors: Paula DP,Azzoni AR,Siqueira SF,Catani CF,Rosselli LK,de Souza AP

    更新日期:2003-11-01 00:00:00

  • Expression and purification of receptor for activated C-kinase 1 (RACK1).

    abstract::Receptor for activated C-kinase (RACK1) binds to protein kinase C and functions as an anchor for several other cellular components. Most in vitro studies of RACK1 have been carried out with RACK1 fused to a soluble fusion protein partner, such as GST or MBP. Here, we show that fusion complexes may exist as large solub...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/s1046-5928(03)00135-9

    authors: Bjørndal B,Trave G,Hageberg I,Lillehaug JR,Raae AJ

    更新日期:2003-09-01 00:00:00

  • Purification and partial characterization of acyl carrier protein from Euglena gracilis variety bacillaris.

    abstract::Acyl carrier protein (ACP) was purified from Euglena gracilis variety bacillaris in yields of about 1 mg/100 g (wet wt) of cells. Antibodies against the purified protein were raised in hens and isolated from eggs. Antibodies raised against Euglena ACP inhibited the Euglena chloroplast nonaggregated fatty acid syntheta...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/1046-5928(91)90072-q

    authors: Williams SG,Worsham LM,Ernst-Fonberg ML

    更新日期:1991-04-01 00:00:00

  • Method for efficient soluble expression and purification of recombinant human interleukin-15.

    abstract::Periplasmic expression of recombinant proteins ensures the production of biologically active proteins in a correctly folded state with several key advantages. This research focused on the in-frame cloning of rhIL-15 in pET-20 (+) vector with pelB-leader sequence to direct the protein to the bacterial periplasm. The ta...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2020.105746

    authors: Ahmed N,Afroze B,Abbas R,Khan MA,Akram M,Tahir S,Bakht S,Munir A,Shahid AA

    更新日期:2021-01-01 00:00:00

  • Rapid generation of stable cell lines expressing corticotropin-releasing hormone receptor for drug discovery.

    abstract::Human HEK293 cells that stably express the Epstein Barr nuclear antigen 1 (EBNA1) support the episomal replication of plasmids containing the Epstein Barr virus origin of replication (EBV oriP). A 293EBNA (293E) cell line expressing the human corticotropin-releasing hormone receptor subtype I (CRHR1) from an episomal ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1996.0701

    authors: Horlick RA,Sperle K,Breth LA,Reid CC,Shen ES,Robbins AK,Cooke GM,Largent BL

    更新日期:1997-04-01 00:00:00

  • Overexpression and purification of the Escherichia coli inner membrane enzyme acyl-acyl carrier protein synthase in an active form.

    abstract::Acyl-acyl carrier protein synthase (Aas) is widely used to synthesize thioester adducts of fatty acids between 8 and 18 carbons in length enzymatically to the phosphopantetheine group of acyl carrier protein. The enzyme is an 80.6-kDa inner membrane protein that functions in vivo as a 2-acylglycerophosphoethanolamine ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.2000.1206

    authors: Shanklin J

    更新日期:2000-04-01 00:00:00

  • Cloning, expression, purification, and biochemical characterisation of the FIC motif containing protein of Mycobacterium tuberculosis.

    abstract::The role of FIC (Filamentation induced by cAMP)(2) domain containing proteins in the regulation of many vital pathways, mostly through the transfer of NMPs from NTPs to specific target proteins (NMPylation), in microorganisms, higher eukaryotes, and plants is emerging. The identity and function of FIC domain containin...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2012.08.020

    authors: Mishra S,Bhagavat R,Chandra N,Vijayarangan N,Rajeswari H,Ajitkumar P

    更新日期:2012-11-01 00:00:00

  • High-level expression and characterization of Fusarium solani cutinase in Pichia pastoris.

    abstract::High-level extracellular production of Fusarium solani cutinase was achieved using a Pichia pastoris expression system. The cutinase-encoding gene was cloned into pPICZalphaA with the Saccharomyces cerevisiae alpha-factor signal sequence and methanol-inducible alcohol oxidase promoter by two different ways. The additi...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2009.06.021

    authors: Kwon MA,Kim HS,Yang TH,Song BK,Song JK

    更新日期:2009-11-01 00:00:00

  • Production and characterization of biologically active human GM-CSF secreted by genetically modified plant cells.

    abstract::Human granulocyte-macrophage colony-stimulating factor (GM-CSF), a hemopoietic growth factor, was produced and secreted from tobacco cell suspensions. The GM-CSF cDNA was carried by a binary vector under the control of the CaMV 35S promoter and the T7 terminator. In addition, a 5'-nontranslated region from the tobacco...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.2000.1232

    authors: James EA,Wang C,Wang Z,Reeves R,Shin JH,Magnuson NS,Lee JM

    更新日期:2000-06-01 00:00:00

  • Heat stability of Proteobacterial PII protein facilitate purification using a single chromatography step.

    abstract::The P(II) proteins comprise a family of widely distributed signal transduction proteins that integrate the signals of cellular nitrogen, carbon and energy status, and then regulate, by protein-protein interaction, the activity of a variety of target proteins including enzymes, transcriptional regulators and membrane t...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2011.09.008

    authors: Moure VR,Razzera G,Araújo LM,Oliveira MAS,Gerhardt ECM,Müller-Santos M,Almeida F,Pedrosa FO,Valente AP,Souza EM,Huergo LF

    更新日期:2012-01-01 00:00:00

  • Coexpression of G-CSF with an unglycosylated G-CSF receptor mutant results in secretion of a stable complex.

    abstract::Previously, we have shown that the entire extracellular domain of the granulocyte-colony stimulating factor receptor (sG-CSFr) produced in Chinese hamster ovary (CHO) cells forms a stable complex with its ligand G-CSF, at a stoichiometry of 2:2. A truncated receptor molecule consisting of the cytokine receptor homolog...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1998.0942

    authors: Horan TP,Simonet L,Jacobsen R,Mann M,Haniu M,Wen J,Arakawa T,Kuwamoto M,Martin F

    更新日期:1998-10-01 00:00:00

  • Heterologous expression of the avirulence gene product, NIP1, from the barley pathogen Rhynchosporium secalis.

    abstract::NIP1, the product of the avirulence gene AvrRrs1 from Rhynchosporium secalis, a fungal pathogen of barley, is a small secreted cysteine-rich protein. This protein is essential for the specific recognition of the fungus by host plants carrying the complementary resistance gene Rrs1. Different heterologous expression sy...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1999.1098

    authors: Gierlich A,van 't Slot KA,Li VM,Marie C,Hermann H,Knogge W

    更新日期:1999-10-01 00:00:00

  • Expression and purification of stable 33-kDa soluble human CD23 using the Drosophila S2 expression system.

    abstract::CD23, a 45-kDa type II membrane glycoprotein present on B cells, monocytes, and other human immune cells, is a low-affinity receptor for IgE. The extracellular region of the membrane-bound human CD23 is processed into at least four soluble (s) CD23 forms, with apparent molecular masses of 37, 33, 29, and 25 kDa. High ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.2001.1448

    authors: Khandekar SS,Mayer RJ,Cusimano DM,Katchur SR,Appelbaum ER

    更新日期:2001-07-01 00:00:00

  • Secretory expression and purification of Aspergillus niger glucose oxidase in Saccharomyces cerevisiae mutant deficient in PMR1 gene.

    abstract::The gene encoding glucose oxidase (GOD) from Aspergillus niger was expressed as a secretory product in the yeast Saccharomyces cerevisiae. Six consecutive histidine residues were fused to the C-terminus of GOD to facilitate purification. The recombinant GOD-His(6) secreted by S. cerevisiae migrated as a broad diffuse ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/s1046-5928(02)00035-9

    authors: Ko JH,Hahm MS,Kang HA,Nam SW,Chung BH

    更新日期:2002-08-01 00:00:00

  • High-throughput proteomics: protein expression and purification in the postgenomic world.

    abstract::Proteomics has become a major focus as researchers attempt to understand the vast amount of genomic information. Protein complexity makes identifying and understanding gene function inherently difficult. The challenge of studying proteins in a global way is driving the development of new technologies for systematic an...

    journal_title:Protein expression and purification

    pub_type: 杂志文章,评审

    doi:10.1006/prep.2001.1465

    authors: Lesley SA

    更新日期:2001-07-01 00:00:00

  • Functional expression and characterization of the myrosinase MYR1 from Brassica napus in Saccharomyces cerevisiae.

    abstract::Myrosinases are thioglucosidases that hydrolyze the natural plant products glucosinolates. We have expressed the myrosinase MYR1 from Brassica napus in Saccharomyces cerevisiae. The recombinant myrosinase was enzymatically active which shows that the MYR1, which in the plant is complex bound with myrosinase-binding pr...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1999.1158

    authors: Chen S,Halkier BA

    更新日期:1999-12-01 00:00:00

  • Enhancing the soluble expression of an amylase in Escherichia coli by the mutations related to its domain interactions.

    abstract::The sequence and structure of the target protein exert a marked effect on its soluble expression in Escherichia coli. The effects of the mutation of an amylase isolated from Bacillus licheniformis (BLA) on its soluble expression in E. coli were investigated. A random mutation library of BLA was constructed to screen f...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2015.12.010

    authors: Wang P,Qin W,Xu J,Yan Y,Tian J,Wu N,Yao B

    更新日期:2016-04-01 00:00:00

  • Novel self-cleavage activity of Staphylokinase fusion proteins: An interesting finding and its possible applications.

    abstract::Staphylokinase (SAK) is reported to have a serine protease domain with no proteolytic activity unlike other plasminogen activators like tissue plasminogen activator (t-PA) and urokinase. A unique protease property of Staphylokinase was observed when SAK was expressed as a fusion protein in inducible Escherichia coli e...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2009.07.011

    authors: Prasad B,Salunkhe SS,Padmanabhan S

    更新日期:2010-02-01 00:00:00

  • Co-expression as a convenient method for the production and purification of core histones in bacteria.

    abstract::Co-expression offers an important strategy for producing multiprotein complexes for biochemical and biophysical studies. We have found that co-expression of histones H2A and H2B (from yeast, chicken or Drosophila) leads to production of soluble heterodimeric H2AH2B complexes. Drosophila histones H3 and H4 can also be ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2010.03.013

    authors: Anderson M,Huh JH,Ngo T,Lee A,Hernandez G,Pang J,Perkins J,Dutnall RN

    更新日期:2010-08-01 00:00:00

  • Improved expression and characterization of Ca2+-ATPase and phospholamban in High-Five cells.

    abstract::The Ca2+-ATPase accounts for the majority of Ca2+ removed from the cytoplasm during cardiac muscle relaxation. The Ca2+-ATPase is regulated by phospholamban, a 52 amino acid phosphoprotein, which inhibits Ca2+-ATPase activity by decreasing the apparent affinity of the ATPase for Ca2+. To study the physical mechanism o...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2003.11.005

    authors: Waggoner JR,Huffman J,Griffith BN,Jones LR,Mahaney JE

    更新日期:2004-03-01 00:00:00

  • Baculovirus expression and purification of a soluble, mutant G-protein alpha subunit.

    abstract::The cDNA for the alpha i1 protein that had undergone site-directed mutagenesis to change glycine-2 to alanine was ligated into a baculovirus transfer vector. A recombinant virus was obtained by transfecting Sf9 cells with both the wild-type baculovirus DNA and the transfer vector and screening for recombinant plaques....

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1993.1010

    authors: Jones TL,Woodard C,Spiegel AM

    更新日期:1993-02-01 00:00:00

  • Methods for preparation of recombinant cytokine proteins V. mutant analogues of human interferon-gamma with higher stability and activity.

    abstract::Mutant analogues of recombinant human immune interferon (IFN-gamma) with higher stability and biological activity were prepared. Depending on the analogue, protein structure modification might involve introduction of an intramonomer disulfide bond (through replacements of Glu7Cys and Ser69Cys), C-terminal shortening b...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.2001.1565

    authors: Pechenov SE,Tikhonov RV,Shingarova LN,Korobko VG,Yakimov SA,Klyushnichenko VE,Babajantz AA,Beliaev DL,Kuznetzov VP,Shvetz VI,Wulfson AN

    更新日期:2002-03-01 00:00:00

  • Cloning, expression and functional characterization of two sesquiterpene synthase genes from moso bamboo (Phyllostachys edulis).

    abstract::The purpose of this work was to characterize the functions of two sesquiterpene synthase genes from moso bamboo (Phyllostachys edulis). Two novel sesquiterpene synthase genes, belonging to the Tpsa subfamily, were isolated from moso bamboo. MoTPS2 was 1641 bp in length and encoded a protein of 63 kDa, whereas MoTPS6 w...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2015.11.019

    authors: Chen X,Wang Y,Sun J,Wang J,Xun H,Tang F

    更新日期:2016-04-01 00:00:00

  • Construction of high-density display of CD147 ectodomain on VCSM13 phage via gpVIII: effects of temperature, IPTG, and helper phage infection-period.

    abstract::Production of VCSM13 phage displaying a high density of CD147 ectodomain (CD147Ex) was achieved when culturing conditions were modulated. A phagemid expressing CD147Ex was constructed and used to produce phage display CD147Ex gpVIII fusion protein in TG1 Escherichia coli. Displaying of CD147Ex via gpVIII was successfu...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2003.08.019

    authors: Intasai N,Arooncharus P,Kasinrerk W,Tayapiwatana C

    更新日期:2003-12-01 00:00:00

  • Generation and application of a 293 cell line stably expressing bovine interferon-gamma.

    abstract::A stable mammalian cell line expressing highly active bovine interferon-gamma (BoIFN-γ) was generated using Flp recombinase-mediated integration. This recombinant 293 cell line (B1) efficiently secreted FLAG-tagged BoIFN-γ protein into the culture supernatant, as determined by ELISA and Western blot. The recombinant B...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2014.04.012

    authors: Xu Z,Shan F,Shan F,Meng C,Zhou X,Zhang X,Chen X,Jiao X

    更新日期:2014-07-01 00:00:00

  • The identification and expression of the full-length HtrA2 gene from Penaeus monodon (black tiger shrimp).

    abstract::HtrA2 is an apoptosis-activating protein to enhance the apoptotic process by preventing the formation of the IAP-caspase complex, thus freeing caspase to trigger the apoptosis pathway. Here, we presented the full-length sequence of HtrA2 from the black tiger shrimp (PmHtrA2). The full-length PmHtrA2 transcript was 140...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2013.09.012

    authors: Suwannaboon R,Phiwsaiya K,Senapin S,Khunrae P,Rattanarojpong T

    更新日期:2013-12-01 00:00:00