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

Citation
Wq. Pan et al., 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, NUCL ACID R, 27(4), 1999, pp. 1094-1103
Citations number
39
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEIC ACIDS RESEARCH
ISSN journal
03051048 → ACNP
Volume
27
Issue
4
Year of publication
1999
Pages
1094 - 1103
Database
ISI
SICI code
0305-1048(19990215)27:4<1094:VCMFPF>2.0.ZU;2-S
Abstract
The Plasmodium falciparum malaria parasite is the causative agent of malari a tropica, Merozoites, one of the extracellular developmental stages of thi s parasite, expose at their surface the merozoite surface protein-1 complex (MSP-1), which results from the proteolytic processing of a 190-200 kDa pr ecursor. 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 m sp-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 c oli and consequently its expression in heterologous systems. Here, we descr ibe 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 ge ne (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 appea rs to possess native conformation because it reacts with a panel of mAbs sp ecific for conformational epitopes, The strategy we used for synthesizing t he full-length msp-1 gene was to assemble it from DNA fragments encoding al l of the major proteolytic fragments normally generated at the parasite's s urface, Thus, after subcloning we also obtained each of these MSP-1 process ing products as hexahistidine fusion proteins in E.coli and isolated them b y affinity chromatography on Ni2+ agarose, The availability of defined prep arations of MSP-1 and its major processing products open up new possibiliti es for in-depth studies at the structural and functional level of this impo rtant protein, including the exploration of MSP-1-based experimental vaccin es.