Isolation and characterisation of the rabies virus N°-P complex produced in insect cells

被引:52
作者
Mavrakis, M
Iseni, F
Mazza, C
Schoehn, G
Ebel, C
Gentzel, M
Franz, T
Ruigrok, RWH
机构
[1] European Mol Biol Lab, Grenoble Outstn, F-38042 Grenoble 9, France
[2] Univ Geneva, Sch Med, CMU, Dept Microbiol, CH-1211 Geneva, Switzerland
[3] UJF, CNRS, CEA, UMR 5075,Inst Biol Struct, F-38027 Grenoble 1, France
[4] European Mol Biol Lab, Bioanalyt Res Grp, D-69117 Heidelberg, Germany
[5] Univ Grenoble 1, EA 2939, Lab Virol Mol & Struct, Grenoble, France
关键词
D O I
10.1006/viro.2002.1748
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
When the nucleoprotein (N) of nonsegmented negative-strand RNA viruses is expressed in insect cells, it binds to cellular RNA and forms N-RNA complexes just like viral nucleocapsids. However, in virus-infected cells, N is prevented from binding to cellular RNA because a soluble complex is formed between IN and the viral phosphoprotein (P), the Ndegrees-P complex. N is only released from this complex for binding to newly made viral or complementary RNA. We coexpressed rabies virus IN and P proteins in insect cells and purified the Ndegrees-P complex. Characterisation by gel filtration, polyacrylamide gel electrophoresis, analytical ultra centrifugation, native mass spectroscopy, and electron microscopy showed that the complex consists of one N protein plus two P proteins, i.e., an Ndegrees-P-2 complex. (C) 2003 Elsevier Science (USA).
引用
收藏
页码:406 / 414
页数:9
相关论文
共 38 条
[1]   IN-VIVO INTERACTION OF RABIES VIRUS PHOSPHOPROTEIN (P) AND NUCLEOPROTEIN (N) - EXISTENCE OF 2 N-BINDING SITES ON P-PROTEIN [J].
CHENIK, M ;
CHEBLI, K ;
GAUDIN, Y ;
BLONDEL, D .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :2889-2896
[2]   MRC image processing programs [J].
Crowther, RA ;
Henderson, R ;
Smith, JM .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :9-16
[3]   AN N-TERMINAL DOMAIN OF THE SENDAI PARAMYXOVIRUS P-PROTEIN ACTS AS A CHAPERONE FOR THE NP PROTEIN DURING THE NASCENT CHAIN ASSEMBLY STEP OF GENOME REPLICATION [J].
CURRAN, J ;
MARQ, JB ;
KOLAKOFSKY, D .
JOURNAL OF VIROLOGY, 1995, 69 (02) :849-855
[4]   AN ACIDIC ACTIVATION-LIKE DOMAIN OF THE SENDAI VIRUS-P PROTEIN IS REQUIRED FOR RNA-SYNTHESIS AND ENCAPSIDATION [J].
CURRAN, J ;
PELET, T ;
KOLAKOFSKY, D .
VIROLOGY, 1994, 202 (02) :875-884
[5]   PARAMYXOVIRUS PHOSPHOPROTEINS FORM HOMOTRIMERS AS DETERMINED BY AN EPITOPE DILUTION ASSAY, VIA PREDICTED COILED COILS [J].
CURRAN, J ;
BOECK, R ;
LINMARQ, N ;
LUPAS, A ;
KOLAKOFSKY, D .
VIROLOGY, 1995, 214 (01) :139-149
[6]   VESICULAR STOMATITIS VIRUS-N AND NS PROTEINS FORM MULTIPLE COMPLEXES [J].
DAVIS, NL ;
ARNHEITER, H ;
WERTZ, GW .
JOURNAL OF VIROLOGY, 1986, 59 (03) :751-754
[7]  
EMERSON SU, 1987, RHABDOVIRUSES, P245
[8]   SPIDER and WEB: Processing and visualization of images in 3D electron microscopy and related fields [J].
Frank, J ;
Radermacher, M ;
Penczek, P ;
Zhu, J ;
Li, YH ;
Ladjadj, M ;
Leith, A .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :190-199
[9]   BOTH THE N-TERMINAL AND THE C-TERMINAL DOMAINS OF THE NOMINAL PHOSPHOPROTEIN OF RABIES VIRUS ARE INVOLVED IN BINDING TO THE NUCLEOPROTEIN [J].
FU, ZF ;
ZHENG, YM ;
WUNNER, WH ;
KOPROWSKI, H ;
DIETZSCHOLD, B .
VIROLOGY, 1994, 200 (02) :590-597
[10]   The transcriptional form of the phosphoprotein of vesicular stomatitis virus is a trimer: Structure and stability [J].
Gao, Y ;
Greenfield, NJ ;
Cleverley, DZ ;
Lenard, J .
BIOCHEMISTRY, 1996, 35 (46) :14569-14573