Source:http://linkedlifedata.com/resource/pubmed/id/15479084
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
41
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pubmed:dateCreated |
2004-10-13
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pubmed:abstractText |
Toward the site-specific incorporation of amino acid analogues into proteins, a two-unnatural-base-pair system was developed for coupled transcription-translation systems with the expanded genetic code. A previously designed unnatural base pair between 2-amino-6-(2-thienyl)purine (denoted by s) and pyridin-2-one (denoted by y) was used for the site-specific incorporation of yTP into RNA opposite s in templates by T7 RNA polymerase. For the site-specific incorporation of sTP into RNA, a newly developed unnatural base, imidazolin-2-one (denoted by z), is superior to y as a template base for pairing with s in T7 transcription. The combination of the s-y and s-z pairs provides a powerful tool to prepare both y-containing mRNA and s-containing tRNA for efficient coupled transcription-translation systems, in which the genetic code is expanded by the codon-anticodon interactions mediated by the s-y pair. In addition, the nucleoside of s is strongly fluorescent, and thus the s-z pair enables the site-specific fluorescent labeling of RNA molecules. These unnatural-base-pair studies provide valuable information for understanding the mechanisms of replication and transcription.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2-amino-6-(2-thienyl)purine,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Directed RNA Polymerases,
http://linkedlifedata.com/resource/pubmed/chemical/Purines,
http://linkedlifedata.com/resource/pubmed/chemical/Pyridones,
http://linkedlifedata.com/resource/pubmed/chemical/RNA,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Transfer,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/bacteriophage T7 RNA polymerase
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0002-7863
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
126
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
13298-305
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15479084-Base Pairing,
pubmed-meshheading:15479084-Base Sequence,
pubmed-meshheading:15479084-DNA-Directed RNA Polymerases,
pubmed-meshheading:15479084-Genetic Code,
pubmed-meshheading:15479084-Molecular Sequence Data,
pubmed-meshheading:15479084-Nucleic Acid Conformation,
pubmed-meshheading:15479084-Purines,
pubmed-meshheading:15479084-Pyridones,
pubmed-meshheading:15479084-RNA,
pubmed-meshheading:15479084-RNA, Messenger,
pubmed-meshheading:15479084-RNA, Transfer,
pubmed-meshheading:15479084-Transcription, Genetic,
pubmed-meshheading:15479084-Viral Proteins
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pubmed:year |
2004
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pubmed:articleTitle |
A two-unnatural-base-pair system toward the expansion of the genetic code.
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pubmed:affiliation |
Research Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan. ihirao@postman.riken.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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