A dumbbell double nicked duplex dodecamer DNA with a PEG6 tether.

نویسندگان

  • Karolina Hyz
  • Wojciech Bocian
  • Robert Kawęcki
  • Elżbieta Bednarek
  • Jerzy Sitkowski
  • Lech Kozerski
چکیده

A hairpin dodecamer DNA motif with a dangling end composed of four bases was studied in order to find conditions which promote a dumbbell structure as the sole form in solution. It could be used as a model of a DNA duplex with two nicks on opposite strands, mimicking a target for topo II poisons. We have established two alternative means of obtaining a dumbbell in solution as the only form present at 0 °C. The first one is to use a relatively high concentration of a hairpin motif, ca. 3.5 mM, at low ionic strength, and second is to use a moderate hairpin motif concentration of ca. 2 mM at high ionic strength, 200 mM and 15% of methanol. An NMR-derived structure in a buffered water solution is presented. A representative structure ensemble of 10 structures was obtained from MD calculations utilizing the AMBER protocol and using NOESY-derived experiment cross peak volumes transferred to experimental restraints by the MARDIGRAS algorithm.

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DNA Synthesis on a Double-stranded DNA Template by the T4 Bacteriophage DNA Polymerase and the T4 Gene 32 DNA Unwinding Protein

T4 DNA polymerase cannot use a nicked duplex DNA molecule as a template-primer for DNA synthesis, apparently because it is unable to displace the 5’ end of the strand paired to the strand serving as the template. Addition of the T4 phage gene 32 DNA unwinding protein (32-protein) facilities strand displacement and allows the T4 DNA polymerase to synthesize DNA using nicked duplex T7 DNA as the ...

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DNA Synthesis on a Double-stranded DNA Template by the T4 Bacteriophage DNA Polymerase and the T4 Gene 32 DNA Unwinding Protein

T4 DNA polymerase cannot use a nicked duplex DNA molecule as a template-primer for DNA synthesis, apparently because it is unable to displace the 5’ end of the strand paired to the strand serving as the template. Addition of the T4 phage gene 32 DNA unwinding protein (32-protein) facilities strand displacement and allows the T4 DNA polymerase to synthesize DNA using nicked duplex T7 DNA as the ...

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DNA Synthesis on a Double-stranded DNA Template by the T4 Bacteriophage DNA Polymerase and the T4 Gene 32 DNA Unwinding Protein

T4 DNA polymerase cannot use a nicked duplex DNA molecule as a template-primer for DNA synthesis, apparently because it is unable to displace the 5’ end of the strand paired to the strand serving as the template. Addition of the T4 phage gene 32 DNA unwinding protein (32-protein) facilities strand displacement and allows the T4 DNA polymerase to synthesize DNA using nicked duplex T7 DNA as the ...

متن کامل

DNA Synthesis on a Double-stranded DNA Template by the T4 Bacteriophage DNA Polymerase and the T4 Gene 32 DNA Unwinding Protein

T4 DNA polymerase cannot use a nicked duplex DNA molecule as a template-primer for DNA synthesis, apparently because it is unable to displace the 5’ end of the strand paired to the strand serving as the template. Addition of the T4 phage gene 32 DNA unwinding protein (32-protein) facilities strand displacement and allows the T4 DNA polymerase to synthesize DNA using nicked duplex T7 DNA as the ...

متن کامل

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عنوان ژورنال:
  • Organic & biomolecular chemistry

دوره 9 12  شماره 

صفحات  -

تاریخ انتشار 2011