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

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

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. © Springer-Verlag 2012.
Original languageEnglish
Pages (from-to)2461-2465
Number of pages5
JournalParasitology Research
Volume111
Issue number6
DOIs
StatePublished - Dec 1 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Cite this