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PMID: 16719445 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

An efficiently extended class of unnatural base pairs.

Journal of the American Chemical Society ·Vol. 128 ·No. 21 ·2006-05-31 ·Pages 6780-1

Leconte AM, Matsuda S, Romesberg FE

Abstract

A third DNA base pair, which is synthesized efficiently and selectively, would have wide ranging applications from synthetic organisms to nucleic acids biotechnology. Hydrophobic unnatural nucleobases offer a promising route to such a pair, but are often limited by inefficient extension, defined as synthesis immediately following the unnatural pair. Here, we describe a simple screen which enables the characterization of large numbers of previously uncharacterized hetero base pairs. From this screen, we identified a class of unnatural base pairs which are extended more efficiently than any unnatural base pair reported to date. Screening, when complemented by further kinetic analysis, can improve the understanding of the determinants of efficient extension as well as identify viable hetero base pairs.

MeSH Terms
Base Pairing Biochemistry/methods DNA Polymerase I/chemistry Deoxyadenine Nucleotides/chemistry Deoxycytosine Nucleotides/chemistry Nucleotides/chemistry
Chemicals
Deoxyadenine Nucleotides Deoxycytosine Nucleotides Nucleotides 2'-deoxycytidine 5'-triphosphate DNA Polymerase I 2'-deoxyadenosine triphosphate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Leconte Aaron M
Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Matsuda Shigeo
Romesberg Floyd E
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11 references, click to expand
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Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
ISSN
0002-7863
Published
2006-05-31
Pages
6780-1
Language
English
Region
United States
NLM ID
7503056
PMCID
PMC2536686
Subset
IM
Grants
NIGMS NIH HHS · R01 GM060005 · United States
NIGMS NIH HHS · R01 GM060005-07 · United States
NIGMS NIH HHS · GM 60005 · United States
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