Nucleic Acids Research, 1990, Vol. 18, No. 12 3545-3555
© 1990
CHEMISTRY |
Sequence dependent effects in methylphosphonate deoxyribonucleotide double and triple helical complexes
Department of Chemistry and Laboratory for Microbial and Biochemical Sciences, Georgia State University Atlanta, GA 30303-3083 1Applied Biosystems 850 Lincoln Centre Drive, Foster City, CA 94404 2Molecular Pharmacology Laboratory, Food and Drug Administration Bethesda, MD 20892, USA
*To whom correspondence should be addressed
Received March 12, 1990. Revised May 15, 1990. Accepted May 15, 1990.
Deoxyribooligonucleotides containing 19 repeating bases of A, T or U were prepared with normal phosphodiester (dA19, dT19, dU19) or methyl-phosphonate (dA*19, dT*19, dU*19) linkages. Complexes of these strands have been investigated at 1: 1 and 1: 2 molar ratios (purine: pyrimidine) by thermal melting and gel electrophoresis. There are dramatic sequence dependent differences in stabilities of complexes containing methylphosphonate strands. Duplexes of dA*19 with dT19 or dU19 have sharp melting curves, increased Tm values, and slopes of Tm versus log (sodium ion activity) plots reduced by about one half relative to their unmodified ‘parent’ duplexes. Duplexes of dA19 with either dT*19 or dU*19, however, have broader melting curves, reduced Tm values at most salt concentrations and slopes of less than one tenth the values for the unmodified duplexes. Duplex stabilization due to reduced phosphate charge repulsion is offset in the pyrimidine methylphosphonate complexes by steric and other substituent effects. Triple helical complexes with dA19 + 2dT19 and dA19 + 2dU19, which can be detected by biphasic melting curves and gel electrophoresis, are stable at increased Na+ or Mg+2 concentrations. Surprisingly, however, no triple helix forms, even at very high salt concentrations, when any normal strand(s) is replaced by a methylphosphonate strand. Since triple helical complexes with methylphosphonates have been reported for shorter oligomers, inhibition with larger oligomers may vary due to their length and extent of substitution.