Incorporation of (alpha-P-borano)-2',3'-dideoxycytidine 5'-triphosphate into DNA by drug-resistant MMLV reverse transcriptase and Taq DNA polymerase.

Nucleosides Nucleotides Nucleic Acids

Department of Chemistry, P.M. Gross Chemical Laboratory, Duke University, Durham, North Carolina 27708-0346, USA.

Published: December 2003

The Rp-stereoisomer of 5'-(alpha-P-borano)triphosphates of 2'-deoxycytidine (Rp-dCTPalphaB) and 2',3'-dideoxycytidine (Rp-ddCTPalphaB) were synthesized. Their steady-state kinetics of incorporation by ddNTP-resistant enzymes, e.g., MMLV reverse transcriptase (RT) and Taq DNA polymerase, were investigated and compared with incorporation of dCTP and ddCTP. The alpha-boranophosphate substitution in ddCTP results in a 28-fold increase in efficiency of incorporation of the Rp-ddCTPalphaB isomer by MMLV RT, yet has minimal effect on the efficiency of incorporation by Taq DNA polymerase.

Download full-text PDF

Source
http://dx.doi.org/10.1081/NCN-120023091DOI Listing

Publication Analysis

Top Keywords

taq dna
12
dna polymerase
12
mmlv reverse
8
reverse transcriptase
8
transcriptase taq
8
efficiency incorporation
8
incorporation
5
incorporation alpha-p-borano-2'3'-dideoxycytidine
4
alpha-p-borano-2'3'-dideoxycytidine 5'-triphosphate
4
dna
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!