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
References (11)
11 references, click to expand
-
Exploration of factors driving incorporation of unnatural dNTPS into DNA by Klenow fragment (DNA polymerase I) and DNA polymerase alpha.
Nucleic Acids Res. 2005;33(8):2620-8
PMID: 15879351
-
Kinetics of DNA polymerase I (Klenow fragment exo-) activity on damaged DNA templates: effect of proximal and distal template damage on DNA synthesis.
Biochemistry. 1997 Dec 9;36(49):15336-42
PMID: 9398262
-
Probing the active site tightness of DNA polymerase in subangstrom increments.
Proc Natl Acad Sci U S A. 2005 Nov 1;102(44):15803-8
PMID: 16249340
-
Difluorotoluene, a Nonpolar Isostere for Thymine, Codes Specifically and Efficiently for Adenine in DNA Replication.
J Am Chem Soc. 1997 Feb 26;119(8):2056-2057
PMID: 20737028
-
Minor Groove Interactions between Polymerase and DNA: More Essential to Replication than Watson-Crick Hydrogen Bonds?
J Am Chem Soc. 1999 Feb 14;121(10):2323-2324
PMID: 20852718
-
Efforts to expand the genetic alphabet: identification of a replicable unnatural DNA self-pair.
J Am Chem Soc. 2004 Jun 9;126(22):6923-31
PMID: 15174862
-
Escherichia coli DNA polymerase I (Klenow fragment) uses a hydrogen-bonding fork from Arg668 to the primer terminus and incoming deoxynucleotide triphosphate to catalyze DNA replication.
J Biol Chem. 2004 Aug 6;279(32):33043-6
PMID: 15210707
-
Efficient primer strand extension beyond oxadiazole carboxamide nucleobases.
J Am Chem Soc. 2005 Nov 23;127(46):16000-1
PMID: 16287267
-
Hydrophobicity, shape, and pi-electron contributions during translesion DNA synthesis.
J Am Chem Soc. 2006 Jan 11;128(1):143-9
PMID: 16390141
-
A two-unnatural-base-pair system toward the expansion of the genetic code.
J Am Chem Soc. 2004 Oct 20;126(41):13298-305
PMID: 15479084
-
The effect of minor-groove hydrogen-bond acceptors and donors on the stability and replication of four unnatural base pairs.
J Am Chem Soc. 2003 May 21;125(20):6134-9
PMID: 12785844