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 homology domain and N-terminus Ig-like domain (Ig CRH) behaves quite similarly. Both of these forms of the receptor are highly glycosylated. To address the importance of glycosylation toward receptor activity and stability, and possibly obtain nonglycosylated receptor for crystallization, mutations were made to replace four Asn residues which are N-glycosylated in the truncated receptor. Virtually no receptor was recovered from conditioned media of CHO cells transfected with this mutant construct, although a high-level of mRNA coding for receptor was detected; this mRNA was translated as determined by Western blots of cell lysates. These results indicate that the translated product is apparently not secreted from these cells. Cells transfected with mutant receptor cDNA were cotransfected with a cDNA construct expressing G-CSF in which the single O-glycosylation site was eliminated by mutation. Upon fermentation of the cotransfectants, we observed a large amount of receptor-ligand complex in the conditioned media. The purified unglycosylated complex appeared to be of the same binding stoichiometry and approximate binding affinity as that of complex formed by addition of purified ligand and unmutated receptor. These results show that while glycosylation of sG-CSFr is not necessary for ligand binding, it appears to be crucial in folding and export from the cell.

journal_name

Protein Expr Purif

authors

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

doi

10.1006/prep.1998.0942

subject

Has Abstract

pub_date

1998-10-01 00:00:00

pages

45-53

issue

1

eissn

1046-5928

issn

1096-0279

pii

S1046-5928(98)90942-1

journal_volume

14

pub_type

杂志文章
  • First characterization of extremely halophilic 2-deoxy-D-ribose-5-phosphate aldolase.

    abstract::2-Deoxy-d-ribose-5-phosphate aldolase (DERA) catalyzes the aldol reaction between two aldehydes and is thought to be a potential biocatalyst for the production of a variety of stereo-specific materials. A gene encoding DERA from the extreme halophilic archaeon, Haloarcula japonica, was overexpressed in Escherichia col...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2016.05.009

    authors: Ohshida T,Hayashi J,Satomura T,Kawakami R,Ohshima T,Sakuraba H

    更新日期:2016-10-01 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

  • Protective immunity induced by the vaccination of recombinant Proteus mirabilis OmpA expressed in Pichia pastoris.

    abstract::Proteus mirabilis (P. mirabilis) is a zoonotic pathogen that has recently presented a rising infection rate in the poultry industry. To develop an effective vaccine to protect chickens against P. mirabilis infection, OmpA, one of the major outer membrane proteins of P. mirabilis, was expressed in Pichia pastoris. The ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2014.10.001

    authors: Zhang Y,Yang S,Dai X,Liu L,Jiang X,Shao M,Chi S,Wang C,Yu C,Wei K,Zhu R

    更新日期:2015-01-01 00:00:00

  • Functional Expression and Purification of CYP93C20,a Plant Membrane-Associated Cytochrome P450 from Medicago truncatula.

    abstract::Plants possess very large numbers of biosynthetic cytochrome P450 enzymes. In spite of the importance of these enzymes for the synthesis of bioactive plant secondary metabolites, only two plant P450 structures has been obtained to date. Isoflavone synthase (IFS) is a membrane-associated cytochrome P450 enzyme catalyzi...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2010.11.012

    authors: Chang Z,Wang X,Wei R,Liu Z,Shan H,Fan G,Hu H

    更新日期:2010-12-04 00:00:00

  • Membrane protein expression and production: effects of polyhistidine tag length and position.

    abstract::Polyhistidine tags enable the facile purification of proteins by immobilized metal affinity chromatography (IMAC). Both the type and position of purification tags can affect significantly properties of a protein such as its expression level, behavior in solution, and its ability to form suitable samples (esp. suitable...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2003.10.010

    authors: Mohanty AK,Wiener MC

    更新日期:2004-02-01 00:00:00

  • Separation of native and latent forms of human antithrombin by hydrophobic interaction high-performance liquid chromatography.

    abstract::Hydrophobic interaction high-performance liquid chromatography (HIC-HPLC) was utilized for the separation of native human antithrombin (AT) and a partially denaturated form of AT, known as the latent form (L-AT). The AT used in this study is commercially available (Atenativ, Pharmacia & Upjohn, Sweden) and contains al...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.2000.1349

    authors: Karlsson G,Winge S

    更新日期:2001-02-01 00:00:00

  • A novel recombinant expression and purification approach for the full-length anti-apoptotic membrane protein Bcl-2.

    abstract::Programmed cell death (apoptosis) is an essential mechanism in life that tightly regulates embryogenesis and removal of harmful cells. Besides an extrinsic pathway, an intrinsic (mitochondrial) apoptotic pathway exists where mitochondria are actively involved in cellular clearance in response to internal stress signal...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2020.105628

    authors: Ådén J,Mushtaq AU,Dingeldein A,Wallgren M,Gröbner G

    更新日期:2020-08-01 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

  • Comparative analysis of native and cysteine-deficient HIV-1 reverse transcriptase.

    abstract::To study the subunit structure and the active site of human immunodeficiency virus reverse transcriptase (RT), the enzyme was expressed in E. coli and purified to homogeneity in large quantities. The recombinant enzyme consists of two major polypeptides of 66,000 and 53,000 Da in equimolar amounts and a minor species ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/1046-5928(92)90005-h

    authors: Fischer M,Lifshitz R,Katz T,Liefer I,Ben-Artzi H,Gorecki M,Panet A,Zeelon E

    更新日期:1992-08-01 00:00:00

  • Overexpression of the Bacillus subtilis and circulans xylanases in Escherichia coli.

    abstract::An efficient expression system for a low-molecular mass xylanase in Escherichia coli has been developed. A gene encoding the mature Bacillus circulans (Bc) xylanase was designed to imitate the frequency of degenerate codons used in E. coli. Appropriate degenerate codons were used to create multiple unique restriction ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1993.1026

    authors: Sung WL,Luk CK,Zahab DM,Wakarchuk W

    更新日期:1993-06-01 00:00:00

  • Preventing protein aggregation by its hyper-acidic fusion cognates in Escherichia coli.

    abstract::Preventing protein aggregation is crucial for various protein studies, and has a large potential for remedy of protein misfolding or aggregates-linked diseases. In this study, we demonstrated the hyper-acidic protein fusion partners, which were previously reported to enhance the soluble expression of aggregation-prone...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2011.06.004

    authors: Zou Z,Fan Y,Zhang C

    更新日期:2011-11-01 00:00:00

  • A single-step purification of biologically active recombinant human interleukin-5 from a baculovirus expression system.

    abstract::Recombinant human interleukin-5 (rhIL-5) was expressed in baculovirus-infected insect cells and purified to homogeneity from the culture medium in a single chromatographic step. Beginning with a cDNA encoding the full-length precursor form of human IL-5, including the authentic secretory leader sequence, recombinant b...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1995.1009

    authors: Brown PM,Scheid MP,O'Neill GP,Tagari PC,Nicholson DW

    更新日期:1995-02-01 00:00:00

  • Overexpression, purification, and characterization of a thermostable chitinase (Chi40) from Streptomyces thermoviolaceus OPC-520.

    abstract::A new procedure for the large-scale purification of the recombinant thermostable chitinase (Chi40) cloned from Streptomyces thermoviolaceus in various expression vectors in Escherichia coli is described. Chi40 was overproduced in the cytosolic and secreted forms. The cytosolic form (Chi40c) was highly overproduced and...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.2001.1490

    authors: Christodoulou E,Duffner F,Vorgias CE

    更新日期:2001-10-01 00:00:00

  • Expression, purification and preliminary characterization of glucagon receptor extracellular domain.

    abstract::Glucagon is a pancreatic hormone that plays pivotal roles in regulating glucose homeostasis and metabolism. Glucagon exerts its action by binding to its receptor, glucagon receptor (GCGR), one of class B G-protein coupled receptors (GPCRs). Diabetes is a bihormonal disease in which excessive glucagon secretion is a ma...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2013.04.004

    authors: Wu L,Zhai Y,Lu J,Wang Q,Sun F

    更新日期:2013-06-01 00:00:00

  • Expression in Escherichia coli of the elongation factor 1beta gene and its nucleotide T160C mutant from the archaeon Sulfolobus solfataricus.

    abstract::The guanine nucleotide exchange factor EF-1beta gene from the thermoacidophilic archaeon Sulfolobus solfataricus (SsEF-1beta) was amplified by PCR and cloned into the pT7-7 expression vector. One of four selected clones harbored the T160C nucleotide substitution leading to the Y54H amino acid change in a hydrophobic r...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1997.0806

    authors: Ianniciello G,Masullo M,Raimo G,Arcari P,Bocchini V

    更新日期:1998-02-01 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

  • Expression in Trichoderma reesei and characterisation of a thermostable family 3 beta-glucosidase from the moderately thermophilic fungus Talaromyces emersonii.

    abstract::The gene encoding a thermostable beta-glucosidase (cel3a) was isolated from the thermophilic fungus Talalaromyces emersonii by degenerate PCR and expressed in the filamentous fungus Trichoderma reesei. The cel3a gene encodes an 857 amino acid long protein with a calculated molecular weight of 90.59 kDa. Tal. emersonii...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2004.08.006

    authors: Murray P,Aro N,Collins C,Grassick A,Penttilä M,Saloheimo M,Tuohy M

    更新日期:2004-12-01 00:00:00

  • Expression of bioactive soluble human stem cell factor (SCF) from recombinant Escherichia coli by coproduction of thioredoxin and efficient purification using arginine in affinity chromatography.

    abstract::Stem cell factor (SCF) known as the c-kit ligand is a two disulfide bridge-containing cytokine in the regulation of the development and function of hematopoietic cell lineages and other cells such as mast cells, germ cells, and melanocytes. The secreted soluble form of SCF exists as noncovalently associated homodimer ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2014.09.015

    authors: Akuta T,Kikuchi-Ueda T,Imaizumi K,Oshikane H,Nakaki T,Okada Y,Sultana S,Kobayashi K,Kiyokawa N,Ono Y

    更新日期:2015-01-01 00:00:00

  • Codon engineering for improved antibody expression in mammalian cells.

    abstract::While well established in bacterial hosts, the effect of coding sequence variation on protein expression in mammalian systems is poorly characterized outside of viral proteins or proteins from distant phylogenetic families. The potential impact is substantial given the extensive use of mammalian expression systems in ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2007.05.017

    authors: Carton JM,Sauerwald T,Hawley-Nelson P,Morse B,Peffer N,Beck H,Lu J,Cotty A,Amegadzie B,Sweet R

    更新日期:2007-10-01 00:00:00

  • Discovery of a novel N-iminylamidase activity: substrate specificity, chemicoselectivity and catalytic mechanism.

    abstract::Enzymatic hydrolysis of the N-iminylamide was investigated in this study. An enzyme possessing N-iminylamidase activity from pig liver was purified to electrophoretic homogeneity. This enzyme was also active, however, with imides and appears to be identical to pig liver imidase. The identification was confirmed by cop...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2004.12.008

    authors: Huang CY,Yang YS

    更新日期:2005-03-01 00:00:00

  • Expression of biologically active recombinant pokeweed antiviral protein in methylotrophic yeast Pichia pastoris.

    abstract::Pokeweed antiviral protein (PAP)-I from the spring leaves of Phytolacca americana is a naturally occurring RNA-depurinating enzyme with broad-spectrum antiviral activity. Interest in PAP is growing due to its use as a potential anti-HIV agent. However, the clinical use of native PAP is limited due to inherent difficul...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1999.1181

    authors: Rajamohan F,Doumbia SO,Engstrom CR,Pendergras SL,Maher DL,Uckun FM

    更新日期:2000-03-01 00:00:00

  • Cloning, expression, and purification of recombinant bovine rotavirus hemagglutinin, VP8*, in Escherichia coli.

    abstract::Rotavirus VP8* subunit is the minor trypsin cleavage product of the spike protein VP4, which is the major determinant of the viral infectivity and neutralization. To study the structure-function relationship of this fragment and to obtain type-specific reagents, substantial amounts of this protein are needed. Thus, fu...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2005.09.014

    authors: Favacho AR,Kurtenbach E,Sardi SI,Gouvea VS

    更新日期:2006-04-01 00:00:00

  • Expression, purification and characterization of TMCO1 for structural studies.

    abstract::Transmembrane and coiled-coil domains 1 (TMCO1) has a highly conserved amino acid sequence among species, indicating a critical role of TMCO1 in cell physiology. The deficiency of TMCO1 in humans is associated with cerebrofaciothoracic dysplasia (CFTD), glaucoma, osteogenesis and the occurrence of cancer. TMCO1 was re...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2020.105803

    authors: Zhang N,Tang M,Wen M,Cao Y,OuYang B

    更新日期:2021-03-01 00:00:00

  • The heterologous expression strategies of antimicrobial peptides in microbial systems.

    abstract::Antimicrobial peptides (AMPs) consist of molecules acting on the defense systems of numerous organisms toward tumor and multiple pathogens, such as bacteria, fungi, viruses, and parasites. Compared to traditional antibiotics, AMPs are more stable and have lower propensity for developing resistance through functioning ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章,评审

    doi:10.1016/j.pep.2017.08.003

    authors: Deng T,Ge H,He H,Liu Y,Zhai C,Feng L,Yi L

    更新日期:2017-12-01 00:00:00

  • Rapid one-step isolation of mouse liver catalase by immobilized metal ion affinity chromatography.

    abstract::A novel and rapid procedure for the isolation of catalase from mouse liver, after prior treatment with the peroxisome proliferator perfluorooctanoic acid was developed using immobilized metal ion affinity chromatography involving chelation with zinc ions. The purification developed is simple, rapid (requiring 3 hours ...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1997.0827

    authors: Yang Q,DePierre JW

    更新日期:1998-03-01 00:00:00

  • Improvements of a high-throughput protein purification process using a calcium-dependent setup.

    abstract::The Human Secretome Project aims to produce and purify all human secreted proteins as full-length. In order to enable this, a robust, gentle and effective purification process is needed, where multiple proteins can be purified in parallel. For this reason, a purification system based on a Protein C-tag and the HPC4 an...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2020.105698

    authors: Kanje S,Enstedt H,Dannemeyer M,Uhlén M,Hober S,Tegel H

    更新日期:2020-11-01 00:00:00

  • Heterologous expression of 5'-methylthioadenosine phosphorylase from the archaeon Sulfolobus solfataricus: characterization of the recombinant protein and involvement of disulfide bonds in thermophilicity and thermostability.

    abstract::The gene for the extremely thermophilic and thermostable 5'-methylthioadenosine phosphorylase from the archaeon Sulfolobus solfataricus was expressed at a high level in Escherichia coli thus providing a basis for detailed structural and functional studies of the enzyme. The recombinant enzyme was purified to homogenei...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1006/prep.1999.1076

    authors: Cacciapuoti G,Fusco S,Caiazzo N,Zappia V,Porcelli M

    更新日期:1999-06-01 00:00:00

  • Expression of non-toxic mutant of Escherichia coli heat-labile enterotoxin in tobacco chloroplasts.

    abstract::Chloroplast transformation systems offer unique advantages in biotechnology, including high level of foreign gene expression, maternal inheritance, and polycistronic expression. We studied chloroplast expression of LTK63 (change Ser-->Lys at position 63 in the A subunit) which is the mutant of Escherichia coli heat-la...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2004.08.002

    authors: Kang TJ,Han SC,Kim MY,Kim YS,Yang MS

    更新日期:2004-11-01 00:00:00

  • Domain isolation, expression, purification and proteolytic activity of the metalloprotease PrtV from Vibrio cholerae.

    abstract::The metalloprotease PrtV from Vibrio cholerae serves an important function for the bacteria's ability to invade the mammalian host cell. The protein belongs to the family of M6 proteases, with a characteristic zinc ion in the catalytic active site. PrtV constitutes a 918 amino acids (102 kDa) multidomain pre-pro-prote...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2014.01.012

    authors: Edwin A,Grundström C,Wai SN,Ohman A,Stier G,Sauer-Eriksson AE

    更新日期:2014-04-01 00:00:00

  • Generation and expression of a minimal hybrid Ig-receptor formed between single domains from proteins L and G.

    abstract::The Ig-binding properties of protein L from Peptostreptococcus magnus and protein G from Streptococcus have been successfully combined through the construction of a novel hybrid protein, consisting of a single Ig-binding domain from each protein. The biophysical and biochemical properties of this construct have been c...

    journal_title:Protein expression and purification

    pub_type: 杂志文章

    doi:10.1016/j.pep.2007.11.007

    authors: Harrison SL,Housden NG,Bottomley SP,Cossins AJ,Gore MG

    更新日期:2008-03-01 00:00:00