0 175

Cited 8 times in

Soluble expression in Escherichia coli of murine endogenous retroviral transmembrane envelope protein having immunosuppressive activity.

Authors
Kim, KS; Kim, KH; Choi, SE; Yoon, JW; Kang, Y
Citation
Protein expression and purification, 16(1):19-26, 1999
Journal Title
Protein expression and purification
ISSN
1046-59281096-0279
Abstract
Recently, we cloned a fragment of the endogenous murine leukemia viral envelope gene from beta cell line (MIN6N8a) as a new autoantigen gene, whose product was reactive with nonobese diabetic (NOD) mice sera. As a result of determination of nucleotide sequence, this envelope protein had the CKS-17 peptide sequence having immunosuppressive activity. To investigate the role of our cloned transmembrane envelope protein in the pathogenesis of autoimmune insulin-dependent diabetes mellitus (IDDM) as an autoantigen or immunosuppressive modulator, a high amount of transmembrane envelope protein was essentially required. Therefore, the expression of our cloned retroviral transmembrane envelope gene was tried in Escherichia coli by a pET vector. However, the expression rate was very low (less than 2%) and most of the expressed protein was insoluble. To improve solubility, the hydrophobic transmembrane anchor domain of our envelope gene was deleted and then the expression of the hydrophilic transmembrane envelope protein was carried out by using the same pET expression system. The expressed protein was completely soluble and the expression yield was dramatically improved by around 25-fold increase. The hydrophilic transmembrane envelope protein was purified by one-step Ni-NTA affinity chromatography and then the fusion tag consisting of the six-histidine peptide and S peptide was removed by cleavage with enterokinase. The processed hydrophilic retroviral transmembrane envelope protein was still immune reactive with NOD sera and also showed immunosuppressive activity by down-regulating the Th1-type cytokine (interferon-gamma) and up-regulating the Th2-type cytokine (interleukin 10).
MeSH terms
Amino Acid SequenceAnimalsAutoantigens/geneticsAutoantigens/isolation & purificationBase SequenceCell LineDNA Primers/geneticsDiabetes Mellitus, Type 1/etiologyDiabetes Mellitus, Type 1/immunologyEscherichia coli/genetics*Gene ExpressionGenetic VectorsImmunosuppressive Agents/isolation & purificationInterferon-gamma/metabolismInterleukin-10/metabolismLeukemia Virus, Murine/genetics*Leukemia Virus, Murine/immunology*MiceMice, Inbred NODRecombinant Proteins/geneticsRecombinant Proteins/immunologyRecombinant Proteins/isolation & purificationViral Envelope Proteins/genetics*Viral Envelope Proteins/immunology*Viral Envelope Proteins/isolation & purification
DOI
10.1006/prep.1999.1042
PMID
10336856
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
Journal Papers > School of Medicine / Graduate School of Medicine > Physiology
AJOU Authors
윤, 지원강, 엽
Full Text Link
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse