In vitro human cell-free expression system for synthesis of malaria proteins

被引:2
作者
Yadavalli, R. [1 ]
Ledger, C. [1 ]
Sam-Yellowe, T. Y. [1 ]
机构
[1] Cleveland State Univ, Dept Biol Geol & Environm Sci, Coll Sci & Hlth Profess, Cleveland, OH 44115 USA
关键词
PLASMODIUM-FALCIPARUM; WHEAT-GERM; MEMBRANE; GLYCOSYLATION; PARASITES; VACCINES;
D O I
10.1007/s00436-012-3014-7
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
In this study, we performed cell-free expression of Plasmodium proteins using the in vitro human cell-free protein expression systems for DNA and mRNA. Malaria rhoptry genes (PFc14_0344, PFc0120w, PY01759, PY00763, PY07482, and PY04666) and a Maurer's cleft gene (PfA0680c) identified from proteome analysis studies were cloned into the pT7CFE1-CHis expression vector. Following a coupled transcription-translation procedure, expressed proteins were analyzed by His-tag staining and by western blotting using protein specific antibodies and nickel-horseradish peroxidase (HRP) for histidine detection. Antibodies against whole rhoptries of Plasmodium falciparum and Plasmodium yoelii merozoites and antibodies specific for the PfMC-2TM protein identified translated proteins. The rhoptry specific antibodies exhibited cross reactivity among the expressed proteins of P. falciparum and P. yoelii. The results demonstrate that the in vitro human cell-free protein expression system is suitable for rapid expression and screening of malaria vaccine candidates and diagnostic biomarkers.
引用
收藏
页码:2461 / 2465
页数:5
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