Base pairing involving artificial bases in vitro and in vivo
Author:
Affiliation:
1. Medicinal Chemistry
2. Rega Institute for Medical Research
3. KU Leuven
4. 3000 Leuven
5. Belgium
6. iSSB – CNRS FRE3561
7. University of Evry-Val-d'Essonne
8. F-91030 Évry Cedex
9. France
Abstract
Herein we report the synthesis, base pairing properties and in vivo transliteration of N8-glycosylated 8-aza-deoxyguanosine and 8-aza-9-deaza-deoxyguanosine nucleotides with 8-amino-deoxyinosine, 1-N-methyl-8-amino-deoxyinosine and 7,8-dihydro-8-oxo-deoxy-inosine/adenosine/guanosine as pairing partners.
Funder
European Research Council
Fonds Wetenschappelijk Onderzoek
KU Leuven
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/SC/C5SC03474D
Reference53 articles.
1. Understanding Nucleic Acids Using Synthetic Chemistry
2. A Four-Base Paired Genetic Helix with Expanded Size
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4. Efficient and sequence-independent replication of DNA containing a third base pair establishes a functional six-letter genetic alphabet
5. Highly specific unnatural base pair systems as a third base pair for PCR amplification
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