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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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 |
work_keys_str_mv |
AT arguledagnija invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles AT cielensindulis invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles AT renhofaregina invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles AT strodsarnis invivopackagingofmrnainyeastproducedbacteriophagegaderivedviruslikeparticles |
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1717812790253584384 |