In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles

Bacteriophage GA coat protein formed self-assembly competent virus-like particles (VLPs) have been expressed previously in bacterial and yeast cells. On the basis of our previous experiments on the yeast vector pESC-URA / S. cerevisiae system containing two oppositely oriented promoters, new constru...

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Main Authors: Ārgule Dagnija, Cielēns Indulis, Renhofa Regīna, Strods Arnis
Format: Article
Language:English
Published: Sciendo 2017-08-01
Series:Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
Subjects:
ga
ms2
Online Access:https://doi.org/10.1515/prolas-2017-0045
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spelling doaj-11cbb9a07a124bfab94751a64f743a7e2021-09-05T13:59:55ZengSciendoProceedings of the Latvian Academy of Sciences. Section B, Natural Sciences1407-009X2017-08-0171426627410.1515/prolas-2017-0045prolas-2017-0045In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like ParticlesĀrgule Dagnija0Cielēns Indulis1Renhofa Regīna2Strods Arnis3Latvian Biomedical Research and Study Centre, 1 Rātsupītes Str., Rīga, LV-1067, LatviaLatvian Biomedical Research and Study Centre, 1 Rātsupītes Str., Rīga, LV-1067, LatviaLatvian Biomedical Research and Study Centre, 1 Rātsupītes Str., Rīga, LV-1067, LatviaLatvian Biomedical Research and Study Centre, 1 Rātsupītes Str., Rīga, LV-1067, LatviaBacteriophage GA coat protein formed self-assembly competent virus-like particles (VLPs) have been expressed previously in bacterial and yeast cells. On the basis of our previous experiments on the yeast vector pESC-URA / S. cerevisiae system containing two oppositely oriented promoters, new constructions were created with point-mutations in coat protein to mimic phage MS2-like RNA binding characteristics. Simultaneously, the MS2 operator sequence was added to mRNA desired for packaging. After the introduction of single-point mutations (S87N, K55N, R43K) and double-point mutations (S87N + K55N and S87N + R43K), the coat protein’s ability to form VLPs was retained, but yield from cells was decreased. Exchange of the 87th Ser to Asn in coat protein sequence in combination with bacteriophage MS2 translational operator provided specific packaging of the gene of interest (GFP). Although non-specific nucleic acid sequences were packaged, the remarkable specificity for packaging of the gene of interest can be achieved using the described approach.https://doi.org/10.1515/prolas-2017-0045virus-like particlesgams2operator
collection DOAJ
language English
format Article
sources DOAJ
author Ārgule Dagnija
Cielēns Indulis
Renhofa Regīna
Strods Arnis
spellingShingle Ārgule Dagnija
Cielēns Indulis
Renhofa Regīna
Strods Arnis
In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles
Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
virus-like particles
ga
ms2
operator
author_facet Ārgule Dagnija
Cielēns Indulis
Renhofa Regīna
Strods Arnis
author_sort Ārgule Dagnija
title In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles
title_short In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles
title_full In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles
title_fullStr In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles
title_full_unstemmed In Vivo Packaging of mRNA in Yeast-Produced Bacteriophage GA Derived Virus-Like Particles
title_sort in vivo packaging of mrna in yeast-produced bacteriophage ga derived virus-like particles
publisher Sciendo
series Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
issn 1407-009X
publishDate 2017-08-01
description Bacteriophage GA coat protein formed self-assembly competent virus-like particles (VLPs) have been expressed previously in bacterial and yeast cells. On the basis of our previous experiments on the yeast vector pESC-URA / S. cerevisiae system containing two oppositely oriented promoters, new constructions were created with point-mutations in coat protein to mimic phage MS2-like RNA binding characteristics. Simultaneously, the MS2 operator sequence was added to mRNA desired for packaging. After the introduction of single-point mutations (S87N, K55N, R43K) and double-point mutations (S87N + K55N and S87N + R43K), the coat protein’s ability to form VLPs was retained, but yield from cells was decreased. Exchange of the 87th Ser to Asn in coat protein sequence in combination with bacteriophage MS2 translational operator provided specific packaging of the gene of interest (GFP). Although non-specific nucleic acid sequences were packaged, the remarkable specificity for packaging of the gene of interest can be achieved using the described approach.
topic virus-like particles
ga
ms2
operator
url https://doi.org/10.1515/prolas-2017-0045
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AT cielensindulis invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles
AT renhofaregina invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles
AT strodsarnis invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles
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