<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T22:10:46Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/4746" metadataPrefix="etdms">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/4746</identifier><datestamp>2022-04-29T12:02:48Z</datestamp><setSpec>com_10259_4365</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>com_10259_4883</setSpec><setSpec>col_10259_4366</setSpec><setSpec>col_10259_4884</setSpec></header><metadata><thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.0/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.0/ http://www.ndltd.org/standards/metadata/etdms/1.0/etdms.xsd">
<title>Kinetic evidence for interaction of TMPyP4 with two different G-quadruplex conformations of human telomeric DNA</title>
<creator>Pérez Arnáiz, Cristina</creator>
<creator>Busto Vázquez, Natalia</creator>
<creator>Santolaya, Javier</creator>
<creator>Leal Villalba, José María</creator>
<creator>Barone, Giampaolo</creator>
<creator>García Ruiz, Begoña</creator>
<subject>Tel22 conformations</subject>
<subject>TMPyP4</subject>
<subject>Fast reactions</subject>
<subject>Molecular dynamics</subject>
<description>Background: Stabilization of G-quadruplex helices by small ligands has attracted growing attention because they&#xd;
inhibit the activity of the enzyme telomerase, which is overexpressed in> 80% cancer cells. TMPyP4, one of the&#xd;
most studied G-quadruplex ligands, is used as a model to show that the ligands can exhibit different binding&#xd;
features with different conformations of a human telomeric specific sequence.&#xd;
Methods: UV–Vis, FRET melting Assay, Isothermal Titration Calorimetry, Time-resolved Fluorescence lifetime,&#xd;
T-Jump and Molecular Dynamics.&#xd;
Results: TMPyP4 yields two different complexes with two Tel22 telomeric conformations in the presence of Na+&#xd;
or K+. T-Jump kinetic experiments show that the rates of formation and dissociation of these complexes in the&#xd;
ms time scale differ by one order of magnitude. MD simulations reveal that, in K+ buffer, “hybrid 1” conformation&#xd;
yields kinetic constants on interaction with TMPyP4 one order lower than “hybrid 2”. The binding&#xd;
involves π–π stacking with external loop bases.&#xd;
Conclusions: For the first time we show that for a particular buffer TMPyP4 interacts in a kinetically different&#xd;
way with the two Tel22 conformations even if the complexes formed are thermodynamically indistinguishable.&#xd;
General significance: G-quadruplexes, endowed with technological applications and potential impact on regulation&#xd;
mechanisms, define a new research field. The possibility of building different conformations from same&#xd;
sequence is a complex issue that confers G-quadruplexes very interesting features. The obtaining of reliable&#xd;
kinetic data constitutes an efficient tool to determine reaction mechanisms between conformations and small&#xd;
molecules.</description>
<date>2018-03-08</date>
<date>2019-03-01</date>
<date>2018-03</date>
<type>info:eu-repo/semantics/article</type>
<identifier>0304-4165</identifier>
<identifier>http://hdl.handle.net/10259/4746</identifier>
<identifier>10.1016/j.bbagen.2017.10.020</identifier>
<language>eng</language>
<relation>Biochimica et biophysica acta (BBA) - general subjects. 2018,  V. 1862, n. 3, p. 522-531</relation>
<relation>https://doi.org/10.1016/j.bbagen.2017.10.020</relation>
<relation>info:eu-repo/grantAgreement/“la&#xd;
Caixa” Foundation/OSLC-2012-007</relation>
<relation>info:eu-repo/grantAgreement/MINECO/CTQ2014-58812-C2-2-R</relation>
<relation>info:eu-repo/grantAgreement/JCyL/BU042U16</relation>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 International</rights>
<publisher>Elsevier</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>