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Authordc.contributor.authorUrbina Donoso, Fabiola
Authordc.contributor.authorMorales Pison, Sebastián
Authordc.contributor.authorMaldonado Maldonado, Edio
Admission datedc.date.accessioned2020-11-24T19:01:07Z
Available datedc.date.available2020-11-24T19:01:07Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationPolymers 2020, 12, 1633es_ES
Identifierdc.identifier.other10.3390/polym12081633
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/177866
Abstractdc.description.abstractMulti-subunit enzymes are protein biopolymers that are involved in many cellular processes. The enzyme that carries out the process of transcription of mRNAs is RNA polymerase II (RNAPII), which is a multi-subunit enzyme in eukaryotes. This protein biopolymer starts the transcription from specific sites and is positioned by transcription factors, which form a preinitiation complex (PIC) on gene promoters. To recognize and position the RNAPII and the transcription factors on the gene promoters are needed specific DNA sequences in the gene promoters, which are named promoter elements. Those gene promoter elements can vary and therefore several kinds of promoters exist, however, it appears that all promoters can use a similar pathway for PIC formation. Those pathways are discussed in this review. The in vitro transcribed mRNA can be used as vaccines to fight infectious diseases, e.g., in immunotherapy against cancer and in nanotechnology to deliver mRNA for a missing protein into the cell. We have outlined a procedure to produce an mRNA vaccine against the SARS-CoV-2 virus, which is the causing agent of the big pandemic, COVID-19, affecting human beings all over the world. The potential advantages of using eukaryotic RNAPII to synthetize large transcripts are outlined and discussed. In addition, we suggest a method to cap the mRNA at the 5 ' terminus by using enzymes, which might be more effective than cap analogs. Finally, we suggest the construction of a future multi-talented RNAPII, which would be able to synthetize large mRNA and cap them in the test tube.es_ES
Patrocinadordc.description.sponsorshipCONICYT GRANT ID16I10145es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherMDPIes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourcePolymerses_ES
Keywordsdc.subjectProtein biopolymeres_ES
Keywordsdc.subjectmRNAes_ES
Keywordsdc.subjectTranscriptiones_ES
Keywordsdc.subjectVaccinees_ES
Keywordsdc.subjectImmunotherapyes_ES
Keywordsdc.subjectNanotechnologyes_ES
Títulodc.titleEnzymatic protein biopolymers as a tool to synthetize eukaryotic messenger Ribonucleic Acid (mRNA) with uses in vaccination, immunotherapy and nanotechnologyes_ES
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso abierto
Catalogueruchile.catalogadorctces_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile