The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine

Background: Merozoite surface protein 1 (MSP-1) is a major protein used by the Plasmodium during red blood cells invasion in malaria. MSP-119, one of MSP-1 is highly conserved, and  it is a potential malaria vaccine candidate because the monoclonal antibodies are capable blocking erythrocyte invasi...

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Main Authors: Amino V.A. Kusuma, Apon Z. Mustopa, Wike Z. Mustafawi, Suharsono Suharsono
Format: Article
Language:English
Published: Faculty of Medicine Universitas Indonesia 2018-02-01
Series:Medical Journal of Indonesia
Subjects:
Online Access:http://mji.ui.ac.id/journal/index.php/mji/article/view/2162
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spelling doaj-7d640edbd6d345ebbea5c6664ac523042020-11-25T02:39:24ZengFaculty of Medicine Universitas Indonesia Medical Journal of Indonesia0853-17732252-80832018-02-0126410.13181/mji.v26i4.21621192The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccineAmino V.A. Kusuma0Apon Z. Mustopa1Wike Z. Mustafawi2Suharsono Suharsono3Research Center for Biotechnology, Indonesian Institute of Science (LIPI), BogorResearch Center for Biotechnology, Indonesian Institute of Science (LIPI), BogorResearch Center for Biotechnology, Indonesian Institute of Science (LIPI), BogorResearch Center for Bioresources and Biotechnology, Bogor Agricultural University, Bogor Background: Merozoite surface protein 1 (MSP-1) is a major protein used by the Plasmodium during red blood cells invasion in malaria. MSP-119, one of MSP-1 is highly conserved, and  it is a potential malaria vaccine candidate because the monoclonal antibodies are capable blocking erythrocyte invasion in vitro. The aim of this study was to produce MSP-119 gene construct and the recombinant protein in Lactococcus lactis. Methods: Usp45-MSP-119, derived from codon optimization and the synthetic gene, was inserted into the pMAT cloning vector. A vector expressing MSP-119 included usp45 has been constructed by the manipulation of recombinant DNA using restriction enzymes. The MSP-119 protein was expressed to 45% ammonium sulfate precipitation and purified using Sephadex-G50 gel filtration chromatography. The expressed protein was characterized by SDS-PAGE and dot blot. Results: usp45-MSP-119 gene was amplified using specific primers and inserted into the multiple cloning sites in the expression vector pNZ8148 with size 3,538 bp as a recombinant vector. The protein of  MSP-119 was successfully expressed in L. lactis with molecular weight of 10.45 kDa. The dot blot was tested in 3 different comparisons between the host cells, non-induced cells, and induced cells with 10 ng/ml nisin. The results showed that 10 ng/ml nisin gave a positive reaction as detected by dot blot assay. Conclusion: This study confirmed that the usp45-MSP-119 gene was successfully inserted into the multiple cloning sites of the pNZ8148 expression vector and the MSP-119 protein expressed in the NICE system of the L. lactis host cell. http://mji.ui.ac.id/journal/index.php/mji/article/view/2162Lactococcus lactismalariamerozoite surface protein 1nisinusp45-MSP-119
collection DOAJ
language English
format Article
sources DOAJ
author Amino V.A. Kusuma
Apon Z. Mustopa
Wike Z. Mustafawi
Suharsono Suharsono
spellingShingle Amino V.A. Kusuma
Apon Z. Mustopa
Wike Z. Mustafawi
Suharsono Suharsono
The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine
Medical Journal of Indonesia
Lactococcus lactis
malaria
merozoite surface protein 1
nisin
usp45-MSP-119
author_facet Amino V.A. Kusuma
Apon Z. Mustopa
Wike Z. Mustafawi
Suharsono Suharsono
author_sort Amino V.A. Kusuma
title The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine
title_short The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine
title_full The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine
title_fullStr The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine
title_full_unstemmed The production of SPusp45-MSP-1<sub>19</sub> gene construct and its recombinant protein in <em>Lactococcus lactis</em> to be used as a malaria vaccine
title_sort production of spusp45-msp-1<sub>19</sub> gene construct and its recombinant protein in <em>lactococcus lactis</em> to be used as a malaria vaccine
publisher Faculty of Medicine Universitas Indonesia
series Medical Journal of Indonesia
issn 0853-1773
2252-8083
publishDate 2018-02-01
description Background: Merozoite surface protein 1 (MSP-1) is a major protein used by the Plasmodium during red blood cells invasion in malaria. MSP-119, one of MSP-1 is highly conserved, and  it is a potential malaria vaccine candidate because the monoclonal antibodies are capable blocking erythrocyte invasion in vitro. The aim of this study was to produce MSP-119 gene construct and the recombinant protein in Lactococcus lactis. Methods: Usp45-MSP-119, derived from codon optimization and the synthetic gene, was inserted into the pMAT cloning vector. A vector expressing MSP-119 included usp45 has been constructed by the manipulation of recombinant DNA using restriction enzymes. The MSP-119 protein was expressed to 45% ammonium sulfate precipitation and purified using Sephadex-G50 gel filtration chromatography. The expressed protein was characterized by SDS-PAGE and dot blot. Results: usp45-MSP-119 gene was amplified using specific primers and inserted into the multiple cloning sites in the expression vector pNZ8148 with size 3,538 bp as a recombinant vector. The protein of  MSP-119 was successfully expressed in L. lactis with molecular weight of 10.45 kDa. The dot blot was tested in 3 different comparisons between the host cells, non-induced cells, and induced cells with 10 ng/ml nisin. The results showed that 10 ng/ml nisin gave a positive reaction as detected by dot blot assay. Conclusion: This study confirmed that the usp45-MSP-119 gene was successfully inserted into the multiple cloning sites of the pNZ8148 expression vector and the MSP-119 protein expressed in the NICE system of the L. lactis host cell.
topic Lactococcus lactis
malaria
merozoite surface protein 1
nisin
usp45-MSP-119
url http://mji.ui.ac.id/journal/index.php/mji/article/view/2162
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