author_facet Liberles, D A
Dervan, P B
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Dervan, P B
author Liberles, D A
Dervan, P B
spellingShingle Liberles, D A
Dervan, P B
Proceedings of the National Academy of Sciences
Design of artificial sequence-specific DNA bending ligands.
Multidisciplinary
author_sort liberles, d a
spelling Liberles, D A Dervan, P B 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.93.18.9510 <jats:p>Proteins that bend DNA are important regulators of biological processes. Sequence-specific DNA bending ligands have been designed that bind two noncontiguous sites in the major groove and induce a bend in the DNA. An oligonucleotide containing pyrimidine segments separated by a central variable linker domain simultaneously binds by triple helix formation two 15-bp purine tracts separated by 10 bp. Bend angles of 61 degrees, 50 degrees, and 38 degrees directed towards the minor groove were quantitated by phasing analysis for linkers of four, five, and six T residues, respectively. The design and synthesis of nonnatural architectural factors may provide a new class of reagents for use in biology and human medicine.</jats:p> Design of artificial sequence-specific DNA bending ligands. Proceedings of the National Academy of Sciences
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title Design of artificial sequence-specific DNA bending ligands.
title_unstemmed Design of artificial sequence-specific DNA bending ligands.
title_full Design of artificial sequence-specific DNA bending ligands.
title_fullStr Design of artificial sequence-specific DNA bending ligands.
title_full_unstemmed Design of artificial sequence-specific DNA bending ligands.
title_short Design of artificial sequence-specific DNA bending ligands.
title_sort design of artificial sequence-specific dna bending ligands.
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.93.18.9510
publishDate 1996
physical 9510-9514
description <jats:p>Proteins that bend DNA are important regulators of biological processes. Sequence-specific DNA bending ligands have been designed that bind two noncontiguous sites in the major groove and induce a bend in the DNA. An oligonucleotide containing pyrimidine segments separated by a central variable linker domain simultaneously binds by triple helix formation two 15-bp purine tracts separated by 10 bp. Bend angles of 61 degrees, 50 degrees, and 38 degrees directed towards the minor groove were quantitated by phasing analysis for linkers of four, five, and six T residues, respectively. The design and synthesis of nonnatural architectural factors may provide a new class of reagents for use in biology and human medicine.</jats:p>
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author Liberles, D A, Dervan, P B
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container_issue 18
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description <jats:p>Proteins that bend DNA are important regulators of biological processes. Sequence-specific DNA bending ligands have been designed that bind two noncontiguous sites in the major groove and induce a bend in the DNA. An oligonucleotide containing pyrimidine segments separated by a central variable linker domain simultaneously binds by triple helix formation two 15-bp purine tracts separated by 10 bp. Bend angles of 61 degrees, 50 degrees, and 38 degrees directed towards the minor groove were quantitated by phasing analysis for linkers of four, five, and six T residues, respectively. The design and synthesis of nonnatural architectural factors may provide a new class of reagents for use in biology and human medicine.</jats:p>
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imprint Proceedings of the National Academy of Sciences, 1996
imprint_str_mv Proceedings of the National Academy of Sciences, 1996
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spelling Liberles, D A Dervan, P B 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.93.18.9510 <jats:p>Proteins that bend DNA are important regulators of biological processes. Sequence-specific DNA bending ligands have been designed that bind two noncontiguous sites in the major groove and induce a bend in the DNA. An oligonucleotide containing pyrimidine segments separated by a central variable linker domain simultaneously binds by triple helix formation two 15-bp purine tracts separated by 10 bp. Bend angles of 61 degrees, 50 degrees, and 38 degrees directed towards the minor groove were quantitated by phasing analysis for linkers of four, five, and six T residues, respectively. The design and synthesis of nonnatural architectural factors may provide a new class of reagents for use in biology and human medicine.</jats:p> Design of artificial sequence-specific DNA bending ligands. Proceedings of the National Academy of Sciences
spellingShingle Liberles, D A, Dervan, P B, Proceedings of the National Academy of Sciences, Design of artificial sequence-specific DNA bending ligands., Multidisciplinary
title Design of artificial sequence-specific DNA bending ligands.
title_full Design of artificial sequence-specific DNA bending ligands.
title_fullStr Design of artificial sequence-specific DNA bending ligands.
title_full_unstemmed Design of artificial sequence-specific DNA bending ligands.
title_short Design of artificial sequence-specific DNA bending ligands.
title_sort design of artificial sequence-specific dna bending ligands.
title_unstemmed Design of artificial sequence-specific DNA bending ligands.
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.93.18.9510