<?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>2026-04-17T16:02:27Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2117/12060" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2117/12060</identifier><datestamp>2026-01-30T07:44:20Z</datestamp><setSpec>com_2072_1033</setSpec><setSpec>col_2072_452950</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Key building block of photoresponsive biomimetic systems</dc:title>
   <dc:creator>Revilla López, Guillermo</dc:creator>
   <dc:creator>Laurent,, Adele D.</dc:creator>
   <dc:creator>Perpete, Eric A.</dc:creator>
   <dc:creator>Jacquemin, Denis</dc:creator>
   <dc:creator>Torras Costa, Juan</dc:creator>
   <dc:creator>Assfeld, Xavier</dc:creator>
   <dc:creator>Alemán Llansó, Carlos</dc:creator>
   <dc:contributor>Universitat Politècnica de Catalunya. Departament d'Enginyeria Química</dc:contributor>
   <dc:contributor>Universitat Politècnica de Catalunya. IMEM - Innovació, Modelització i Enginyeria en (BIO) Materials</dc:contributor>
   <dc:subject>Àrees temàtiques de la UPC::Enginyeria química</dc:subject>
   <dc:subject>Biomimetics</dc:subject>
   <dc:subject>Biomimètica</dc:subject>
   <dc:description>The conformational, electrical, and optical intrinsic&#xd;
properties of L-phenylazophenylalanine (L-PAP), a nonproteinogenic&#xd;
photoresponsive amino acid used to modulate the binding&#xd;
affinity and activity of peptides and proteins, have been systematically&#xd;
investigated using quantum mechanical calculations, with&#xd;
special emphasis being put on the trans-to-cis isomerization of the&#xd;
azobenzene side group. Analyses of the conformational maps and&#xd;
the minimum-energy conformations, which were obtained using&#xd;
density functional theory calculations at the B3LYP/6-311þþG(d,&#xd;
p) level, indicate that the semiextended β is the most favored&#xd;
conformation for both the trans and cis isomers in the gas phase.&#xd;
However, water tends to stabilize the helical backbone arrangement,&#xd;
but only for the cis isomer since this is a sterically forbidden&#xd;
conformation for the trans one. On the other hand, time-dependent&#xd;
density functional theory calculations at the BMK/6-311þG(d,p)&#xd;
level indicate that the peptide backbone does not induce significant&#xd;
changes in the optical properties of the chromophore. This feature was evidenced by both the small dependence of the πfπ* and nfπ*&#xd;
transition wavelengths with the backbone dihedral anglesjandψand the resemblance between the transition wavelengths determined for&#xd;
L-PAP and free azobenzene. In contrast, the dipole moment has been identified as a key property for this photoresponsive amino acid&#xd;
because of its large dependence on both the peptide backbone and the isomerization state.</dc:description>
   <dc:description>Peer Reviewed</dc:description>
   <dc:description>Postprint (published version)</dc:description>
   <dc:date>2011-02-10</dc:date>
   <dc:type>Article</dc:type>
   <dc:identifier>Revilla-López, G. [et al.]. Key building block of photoresponsive biomimetic systems. "Journal of physical chemistry B", 10 Febrer 2011, vol. 115, núm. 5, p. 1232-1242.</dc:identifier>
   <dc:identifier>1520-6106</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2117/12060</dc:identifier>
   <dc:identifier>10.1021/jp108341a</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>http://pubs.acs.org/doi/pdfplus/10.1021/jp108341a</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights>
   <dc:rights>Restricted access - publisher's policy</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivs 3.0 Spain</dc:rights>
   <dc:format>11 p.</dc:format>
   <dc:format>application/pdf</dc:format>
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