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Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA Independently of the Nature of the Coordinated Metal
Cyclam was attached to 1-, 2- and 3-pyrrole lexitropsins for the first time through a synthetically facile copper-catalyzed “click” reaction. The corresponding copper and zinc complexes were synthesized and characterized. The ligand and its complexes bound AT-rich DNA selectively over GC-rich DNA, a...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090394/ https://www.ncbi.nlm.nih.gov/pubmed/21573061 http://dx.doi.org/10.1371/journal.pone.0017446 |
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author | Lo, Anthony T. S. Salam, Noeris K. Hibbs, David E. Rutledge, Peter J. Todd, Matthew H. |
author_facet | Lo, Anthony T. S. Salam, Noeris K. Hibbs, David E. Rutledge, Peter J. Todd, Matthew H. |
author_sort | Lo, Anthony T. S. |
collection | PubMed |
description | Cyclam was attached to 1-, 2- and 3-pyrrole lexitropsins for the first time through a synthetically facile copper-catalyzed “click” reaction. The corresponding copper and zinc complexes were synthesized and characterized. The ligand and its complexes bound AT-rich DNA selectively over GC-rich DNA, and the thermodynamic profile of the binding was evaluated by isothermal titration calorimetry. The metal, encapsulated in a scorpion azamacrocyclic complex, did not affect the binding, which was dominated by the organic tail. |
format | Text |
id | pubmed-3090394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30903942011-05-13 Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA Independently of the Nature of the Coordinated Metal Lo, Anthony T. S. Salam, Noeris K. Hibbs, David E. Rutledge, Peter J. Todd, Matthew H. PLoS One Research Article Cyclam was attached to 1-, 2- and 3-pyrrole lexitropsins for the first time through a synthetically facile copper-catalyzed “click” reaction. The corresponding copper and zinc complexes were synthesized and characterized. The ligand and its complexes bound AT-rich DNA selectively over GC-rich DNA, and the thermodynamic profile of the binding was evaluated by isothermal titration calorimetry. The metal, encapsulated in a scorpion azamacrocyclic complex, did not affect the binding, which was dominated by the organic tail. Public Library of Science 2011-05-09 /pmc/articles/PMC3090394/ /pubmed/21573061 http://dx.doi.org/10.1371/journal.pone.0017446 Text en Lo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lo, Anthony T. S. Salam, Noeris K. Hibbs, David E. Rutledge, Peter J. Todd, Matthew H. Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA Independently of the Nature of the Coordinated Metal |
title | Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA
Independently of the Nature of the Coordinated Metal |
title_full | Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA
Independently of the Nature of the Coordinated Metal |
title_fullStr | Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA
Independently of the Nature of the Coordinated Metal |
title_full_unstemmed | Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA
Independently of the Nature of the Coordinated Metal |
title_short | Polyamide-Scorpion Cyclam Lexitropsins Selectively Bind AT-Rich DNA
Independently of the Nature of the Coordinated Metal |
title_sort | polyamide-scorpion cyclam lexitropsins selectively bind at-rich dna
independently of the nature of the coordinated metal |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090394/ https://www.ncbi.nlm.nih.gov/pubmed/21573061 http://dx.doi.org/10.1371/journal.pone.0017446 |
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