Recombinant dengue type 1 virus NS5 protein expressed in Escherichia coli exhibits RNA-dependent RNA polymerase activity

被引:204
作者
Tan, BH
Fu, JL
Sugrue, RJ
Yap, EH
Chan, YC
Tan, YH
机构
[1] NATL UNIV SINGAPORE, INST MOLEC & CELL BIOL, SINGAPORE 119260, SINGAPORE
[2] NATL UNIV SINGAPORE, FAC MED, DEPT MICROBIOL, SINGAPORE 119260, SINGAPORE
关键词
D O I
10.1006/viro.1996.0067
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The complete nonstructural NS5 gene of dengue type 1 virus, Singapore strain S275/90 (D1-S275/90) was expressed in Escherichia coli as a glutathione S-transferase (GST) fusion protein (126 kDa). The GST-NS5 fusion protein was purified and the recombinant NS5 protein released from the fusion protein by thrombin cleavage. The recombinant NS5 had a predicted molecular weight of 100 kDa and reacted with antiserum against D1-S275/90 virus in Western blot analysis. The purified recombinant NS5 protein possessed RNA-dependent RNA polymerase activity which was inhibited (>99%) by antibodies against the recombinant NS5 protein. The polymerase product was shown to be a negative-stranded RNA molecule, of template size, which forms a double-stranded complex with the template RNA. (C) 1996 Academic Press, Inc.
引用
收藏
页码:317 / 325
页数:9
相关论文
共 43 条
[31]  
SHINA M, 1995, 4TH INT S POS STRAND, P69
[32]   SINGLE-STEP PURIFICATION OF POLYPEPTIDES EXPRESSED IN ESCHERICHIA-COLI AS FUSIONS WITH GLUTATHIONE S-TRANSFERASE [J].
SMITH, DB ;
JOHNSON, KS .
GENE, 1988, 67 (01) :31-40
[33]   NUCLEOTIDE-SEQUENCE AT THE 3' END OF JAPANESE ENCEPHALITIS-VIRUS GENOMIC RNA [J].
TAKEGAMI, T ;
WASHIZU, M ;
YASUI, K .
VIROLOGY, 1986, 152 (02) :483-486
[34]   ELECTROPHORETIC TRANSFER OF PROTEINS FROM POLYACRYLAMIDE GELS TO NITROCELLULOSE SHEETS - PROCEDURE AND SOME APPLICATIONS [J].
TOWBIN, H ;
STAEHELIN, T ;
GORDON, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (09) :4350-4354
[35]   POLIOVIRUS RNA-DEPENDENT RNA-POLYMERASE SYNTHESIZES FULL-LENGTH COPIES OF POLIOVIRION RNA, CELLULAR MESSENGER-RNA, AND SEVERAL PLANT-VIRUS RNAS INVITRO [J].
TUSCHALL, DM ;
HIEBERT, E ;
FLANEGAN, JB .
JOURNAL OF VIROLOGY, 1982, 44 (01) :209-216
[36]  
VANDYKE TA, 1982, J BIOL CHEM, V257, P4610
[37]   RNA-STIMULATED NTPASE ACTIVITY ASSOCIATED WITH YELLOW-FEVER VIRUS NS3 PROTEIN EXPRESSED IN BACTERIA [J].
WARRENER, P ;
TAMURA, JK ;
COLLETT, MS .
JOURNAL OF VIROLOGY, 1993, 67 (02) :989-996
[38]   INVITRO SYNTHESIS OF WEST NILE VIRUS PROTEINS INDICATES THAT THE AMINO-TERMINAL SEGMENT OF THE NS3 PROTEIN CONTAINS THE ACTIVE-CENTER OF THE PROTEASE WHICH CLEAVES THE VIRAL POLYPROTEIN AFTER MULTIPLE BASIC-AMINO-ACIDS [J].
WENGLER, G ;
CZAYA, G ;
FARBER, PM ;
HEGEMANN, JH .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :851-858
[39]   THE CARBOXY-TERMINAL PART OF THE NS-3-PROTEIN OF THE WEST NILE FLAVIVIRUS CAN BE ISOLATED AS A SOLUBLE-PROTEIN AFTER PROTEOLYTIC CLEAVAGE AND REPRESENTS AN RNA-STIMULATED NTPASE [J].
WENGLER, G ;
WENGLER, G .
VIROLOGY, 1991, 184 (02) :707-715
[40]   TERMINAL SEQUENCES OF THE GENOME AND REPLICATIVE-FORM RNA OF THE FLAVIVIRUS WEST NILE VIRUS - ABSENCE OF POLY(A) AND POSSIBLE ROLE IN RNA REPLICATION [J].
WENGLER, G ;
WENGLER, G .
VIROLOGY, 1981, 113 (02) :544-555