Vaccine candidate MSP-1 from Plasmodium falciparum:: a redesigned 4917 bp polynucleotide enables synthesis and isolation of full-length protein from Escherichia coli and mammalian cells

被引:63
作者
Pan, WQ [1 ]
Ravot, E [1 ]
Tolle, R [1 ]
Frank, R [1 ]
Mosbach, R [1 ]
Türbachova, I [1 ]
Bujard, H [1 ]
机构
[1] Univ Heidelberg, ZMBH, D-69120 Heidelberg, Germany
关键词
D O I
10.1093/nar/27.4.1094
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Plasmodium falciparum malaria parasite is the causative agent of malaria tropica, Merozoites, one of the extracellular developmental stages of this parasite, expose at their surface the merozoite surface protein-1 complex (MSP-1), which results from the proteolytic processing of a 190-200 kDa precursor. MSP-1 is highly immunogenic in humans and numerous studies suggest that this protein is an effective target for a protective immune response, Although its function is unknown, there are indications that it may play a role during invasion of erythrocytes by merozoites, The parasite-derived msp-1 gene, which is similar to 5000 bp long, contains 74% AT, This high AT content has prevented stable cloning of the full-size gene in Escherichia coli and consequently its expression in heterologous systems. Here, we describe the synthesis of a 4917 bp gene encoding MSP-1 from the FCB-1 strain of P. falciparum adjusted for human codon preferences. The synthetic msp-1 gene (55% AT) was cloned, maintained and expressed in its entirety in E.coli as well as in CHO and HeLa cells. The purified protein is soluble and appears to possess native conformation because it reacts with a panel of mAbs specific for conformational epitopes, The strategy we used for synthesizing the full-length msp-1 gene was to assemble it from DNA fragments encoding all of the major proteolytic fragments normally generated at the parasite's surface, Thus, after subcloning we also obtained each of these MSP-1 processing products as hexahistidine fusion proteins in E.coli and isolated them by affinity chromatography on Ni2+ agarose, The availability of defined preparations of MSP-1 and its major processing products open up new possibilities for in-depth studies at the structural and functional level of this important protein, including the exploration of MSP-1-based experimental vaccines.
引用
收藏
页码:1094 / 1103
页数:10
相关论文
共 39 条
[1]   COREGULATION OF 2 GENE ACTIVITIES BY TETRACYCLINE VIA A BIDIRECTIONAL PROMOTER [J].
BARON, U ;
FREUNDLIEB, S ;
GOSSEN, M ;
BUJARD, H .
NUCLEIC ACIDS RESEARCH, 1995, 23 (17) :3605-3606
[2]  
BERHE S, 1998, THESIS U MARBURG
[3]   A SINGLE FRAGMENT OF A MALARIA MEROZOITE SURFACE PROTEIN REMAINS ON THE PARASITE DURING RED-CELL INVASION AND IS THE TARGET OF INVASION-INHIBITING ANTIBODIES [J].
BLACKMAN, MJ ;
HEIDRICH, HG ;
DONACHIE, S ;
MCBRIDE, JS ;
HOLDER, AA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (01) :379-382
[4]   Immunization of Aotus nancymai with recombinant C terminus of Plasmodium falciparum merozoite surface protein 1 in liposomes and alum adjuvant does not induce protection against a challenge infection [J].
Burghaus, PA ;
Wellde, BT ;
Hall, T ;
Richards, RL ;
Egan, AF ;
Riley, EM ;
Ballou, WP ;
Holder, AA .
INFECTION AND IMMUNITY, 1996, 64 (09) :3614-3619
[5]   A recombinant Baculovirus 42-kilodalton c-terminal fragment of Plasmodium falciparum merozoite surface protein 1 protects Aotus monkeys against malaria [J].
Chang, SP ;
Case, SE ;
Gosnell, WL ;
Kramer, KJ ;
Tam, LQ ;
Hashiro, CQ ;
Nikaido, CM ;
Gibson, HL ;
LeeNg, CT ;
Barr, PJ ;
Yokota, BT ;
Hui, GSN .
INFECTION AND IMMUNITY, 1996, 64 (01) :253-261
[6]   PLASMODIUM-FALCIPARUM - INTRAGENIC RECOMBINATION AND NONRANDOM ASSOCIATIONS BETWEEN POLYMORPHIC DOMAINS OF THE PRECURSOR TO THE MAJOR MEROZOITE SURFACE-ANTIGENS [J].
CONWAY, DJ ;
ROSARIO, V ;
ODUOLA, AMJ ;
SALAKO, LA ;
GREENWOOD, BM ;
MCBRIDE, JS .
EXPERIMENTAL PARASITOLOGY, 1991, 73 (04) :469-480
[7]   MEROZOITE SURFACE ANTIGEN-I OF PLASMODIUM [J].
COOPER, JA .
PARASITOLOGY TODAY, 1993, 9 (02) :50-54
[8]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[9]   SERUM ANTIBODIES FROM MALARIA-EXPOSED PEOPLE RECOGNIZE CONSERVED EPITOPES FORMED BY THE 2 EPIDERMAL GROWTH-FACTOR MOTIFS OF MSP1(19), THE CARBOXY-TERMINAL FRAGMENT OF THE MAJOR MEROZOITE SURFACE PROTEIN OF PLASMODIUM-FALCIPARUM [J].
EGAN, AF ;
CHAPPEL, JA ;
BURGHAUS, PA ;
MORRIS, JS ;
MCBRIDE, JS ;
HOLDER, AA ;
KASLOW, DC ;
RILEY, EM .
INFECTION AND IMMUNITY, 1995, 63 (02) :456-466
[10]   ABILITY OF RECOMBINANT OR NATIVE PROTEINS TO PROTECT MONKEYS AGAINST HETEROLOGOUS CHALLENGE WITH PLASMODIUM-FALCIPARUM [J].
ETLINGER, HM ;
CASPERS, P ;
MATILE, H ;
SCHOENFELD, HJ ;
STUEBER, D ;
TAKACS, B .
INFECTION AND IMMUNITY, 1991, 59 (10) :3498-3503