Nucleic Acids Research, Vol 25, Issue 24 5072-5076, Copyright © 1997 by Oxford University Press
S Jacutin, AJ Zhang, DH Russell, RA Gibbs and K Burgess
1-(2'-Deoxy-beta-d-ribofuranosyl)-3-nitropyrrole phosphate was incorporated
into a DNA decamer and analyzed via matrix-assisted laser desorption
ionization mass spectrometry (MALDI-MS). The extent and composition of the
various fragment peaks were compared with those in the MALDI-MS spectrum of
dT4AT5. The nitropyrrole-containing oligomer proved to be more robust. Two
different DNA template assays were then used to attempt to identify DNA
replicating enzymes that would incorporate the corresponding triphosphate,
i.e. 1-(2'-deoxy-beta-d- ribofuranosyl)-3-nitropyrrole triphosphate (dXTP).
It was shown that dXTP was not incorporated by some enzymes and it
inhibited others. However, DNA polymerase I Klenow fragment and avian
myeloblastosis virus reverse transcriptase incorporated dXTP in place of
dATP and then replicated the template overhang in the usual way. The
potential of dXTP as a surrogate for dATP in DNA sequencing with MALDI-MS
analysis is discussed.
ARTICLES
Test of the potential of a dATP surrogate for sequencing via MALDI-MS
Department of Chemistry, Texas A&M University, College Station, TX 77843-3255, USA.
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