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HPLC Purification of In Vitro Transcribed Long RNA | SpringerLink
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In vitro transcription of DNA with phage RNA polymerases is currently the most efficient method to produce long sequence-specific RNA. While the reaction can yield large quantities of RNA, it contains impurities due to various unwanted activities of the polymerases....
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Keywords {🔍}
google, scholar, rna, article, pubmed, cas, mrna, weissman, res, protocol, muramatsu, cells, kariko, nucleic, cell, vitro, human, privacy, cookies, content, information, publish, synthetic, hplc, purification, innate, immune, access, polymerase, ther, acids, search, messenger, transcription, download, usa, springer, usd, personal, data, log, journal, research, metabolism, modulation, transcribed, long, drew, pardi, karikó,
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month download article/chapter suppress rna-mediated activation cell metabolism modulation van kuppeveld fj privacy choices/manage cookies synthetic messenger rna device instant download vitro transcribed rna low-cell-number superior translational capacity generate antineoplastic lymphocytes delivers encoded antigen diminishing pkr activation t7 rna polymerase human disseminated tumor produces mrna free synthetic modified mrna european economic area single-tube amplification metastatic melanoma patients nallagatla sr protein kinase pkr intrinsic cellular defenses nucleic acid contamination nucleic acid precipitation van hout-kuijer de vries ij grant numbers hl87688 author information authors editor information editors mrna encoding erythropoietin protamine-protected mrna protein-encoding mrna journal finder publish conditions privacy policy therapeutic rna development yield large quantities removes multiple contaminants increased translational capacity synthetic dna templates inhibits picornavirus infection chemically modified mrna mrna enhances translation highly efficient reprogramming phage rna polymerases accepting optional cookies formalin-fixed samples pluripotent stem cells molecular biology applications main content log
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ScholarlyArticle:
headline:HPLC Purification of In Vitro Transcribed Long RNA
pageEnd:54
pageStart:43
image:https://media.springernature.com/w153/springer-static/cover/book/978-1-62703-260-5.jpg
genre:
Springer Protocols
isPartOf:
name:Synthetic Messenger RNA and Cell Metabolism Modulation
isbn:
978-1-62703-260-5
978-1-62703-259-9
type:Book
publisher:
name:Humana Press
logo:
url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
type:ImageObject
type:Organization
author:
name:Drew Weissman
affiliation:
name:University of Pennsylvania
address:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
email:[email protected]
type:Person
name:Norbert Pardi
affiliation:
name:University of Pennsylvania
address:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
type:Person
name:Hiro Muramatsu
affiliation:
name:University of Pennsylvania
address:
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
type:Person
name:Katalin Karikó
affiliation:
name:University of Pennsylvania
address:
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
type:Person
keywords:RNA, In vitro transcription, Nucleoside modification, HPLC
description:In vitro transcription of DNA with phage RNA polymerases is currently the most efficient method to produce long sequence-specific RNA. While the reaction can yield large quantities of RNA, it contains impurities due to various unwanted activities of the polymerases. Here, we described an easily performed HPLC purification that removes multiple contaminants from in vitro transcribed RNA and is scalable. The purified RNA is translated at much greater levels, especially in primary cells and in vivo. HPLC purification of RNA containing modified nucleosides that suppress RNA-mediated activation of innate immune sensors leads to a non-immunogenic RNA with superior translational capacity.
datePublished:2013
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Book:
name:Synthetic Messenger RNA and Cell Metabolism Modulation
isbn:
978-1-62703-260-5
978-1-62703-259-9
Organization:
name:Humana Press
logo:
url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
type:ImageObject
name:University of Pennsylvania
address:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
name:University of Pennsylvania
address:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
name:University of Pennsylvania
address:
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
name:University of Pennsylvania
address:
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
ImageObject:
url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
name:Drew Weissman
affiliation:
name:University of Pennsylvania
address:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
email:[email protected]
name:Norbert Pardi
affiliation:
name:University of Pennsylvania
address:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
name:Hiro Muramatsu
affiliation:
name:University of Pennsylvania
address:
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
name:Katalin Karikó
affiliation:
name:University of Pennsylvania
address:
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
type:PostalAddress
type:Organization
PostalAddress:
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
name:Department of Medicine, University of Pennsylvania, Philadelphia, USA
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
name:Department of Neurosurgery, University of Pennsylvania, Philadelphia, USA
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