The influence of pH on the G-quadruplex binding selectivity of perylene derivatives

Three new perylene derivatives with branched ionizable side chains were synthesized, and their G-quadruplex binding specificities were compared by spectroscopic and electrophoretic analysis with two well-studied G-quadruplex ligands: PIPER and TmPyP4. The value of pH and consequent charge formation...

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Main Authors: Tuntiwechapikul W., Taka T., Bethencourt M., Makonkawkeyoon L., Randall Lee T.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-33745141952&partnerID=40&md5=16a2df1db67a778619993a7da18008a2
http://www.ncbi.nlm.nih.gov/pubmed/16713263
http://cmuir.cmu.ac.th/handle/6653943832/2062
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-20622014-08-30T02:00:26Z The influence of pH on the G-quadruplex binding selectivity of perylene derivatives Tuntiwechapikul W. Taka T. Bethencourt M. Makonkawkeyoon L. Randall Lee T. Three new perylene derivatives with branched ionizable side chains were synthesized, and their G-quadruplex binding specificities were compared by spectroscopic and electrophoretic analysis with two well-studied G-quadruplex ligands: PIPER and TmPyP4. The value of pH and consequent charge formation and self-aggregation of these perylene derivatives influences not only the type of G-quadruplex formation, but also the G-quadruplex binding selectivity. © 2006 Elsevier Ltd. All rights reserved. 2014-08-30T02:00:26Z 2014-08-30T02:00:26Z 2006 Article 0960894X 10.1016/j.bmcl.2006.04.078 16713263 BMCLE http://www.scopus.com/inward/record.url?eid=2-s2.0-33745141952&partnerID=40&md5=16a2df1db67a778619993a7da18008a2 http://www.ncbi.nlm.nih.gov/pubmed/16713263 http://cmuir.cmu.ac.th/handle/6653943832/2062 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Three new perylene derivatives with branched ionizable side chains were synthesized, and their G-quadruplex binding specificities were compared by spectroscopic and electrophoretic analysis with two well-studied G-quadruplex ligands: PIPER and TmPyP4. The value of pH and consequent charge formation and self-aggregation of these perylene derivatives influences not only the type of G-quadruplex formation, but also the G-quadruplex binding selectivity. © 2006 Elsevier Ltd. All rights reserved.
format Article
author Tuntiwechapikul W.
Taka T.
Bethencourt M.
Makonkawkeyoon L.
Randall Lee T.
spellingShingle Tuntiwechapikul W.
Taka T.
Bethencourt M.
Makonkawkeyoon L.
Randall Lee T.
The influence of pH on the G-quadruplex binding selectivity of perylene derivatives
author_facet Tuntiwechapikul W.
Taka T.
Bethencourt M.
Makonkawkeyoon L.
Randall Lee T.
author_sort Tuntiwechapikul W.
title The influence of pH on the G-quadruplex binding selectivity of perylene derivatives
title_short The influence of pH on the G-quadruplex binding selectivity of perylene derivatives
title_full The influence of pH on the G-quadruplex binding selectivity of perylene derivatives
title_fullStr The influence of pH on the G-quadruplex binding selectivity of perylene derivatives
title_full_unstemmed The influence of pH on the G-quadruplex binding selectivity of perylene derivatives
title_sort influence of ph on the g-quadruplex binding selectivity of perylene derivatives
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-33745141952&partnerID=40&md5=16a2df1db67a778619993a7da18008a2
http://www.ncbi.nlm.nih.gov/pubmed/16713263
http://cmuir.cmu.ac.th/handle/6653943832/2062
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