Abstract
The replacement of the pyrophosphate moiety of deoxynucleoside triphosphates by L-aspartic acid allows incorporation of natural deoxynucleosides into DNA using HIV reverse transcriptase (RT) as enzyme, while retaining the canonical base-pair selectivity. N-Methylation of the L-aspartic acid leaving group results in a reduced fidelity of incorporation.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Aspartic Acid / chemistry*
-
Catalysis
-
DNA / chemical synthesis*
-
DNA / chemistry
-
Deoxycytidine Monophosphate / chemistry*
-
Deoxyguanine Nucleotides / chemistry*
-
HIV Reverse Transcriptase / chemistry*
-
Methylation
-
Molecular Conformation
-
Molecular Structure
-
Stereoisomerism
-
Thymidine Monophosphate / chemistry*
Substances
-
Deoxyguanine Nucleotides
-
Deoxycytidine Monophosphate
-
Aspartic Acid
-
Thymidine Monophosphate
-
2'-deoxyguanosine 5'-phosphate
-
DNA
-
HIV Reverse Transcriptase