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dc.contributor.authorRamos, Rogeres_ES
dc.contributor.authorManning, Brendan D.es_ES
dc.contributor.authorAviñó, Annaes_ES
dc.contributor.authorGargallo, Raimundoes_ES
dc.contributor.authorEritja Casadellà, Ramónes_ES
dc.date.accessioned2015-11-16T08:11:49Z-
dc.date.available2015-11-16T08:11:49Z-
dc.date.issued2009-04-
dc.identifier.citationHelvetica Chimica Actaes_ES
dc.identifier.urihttp://hdl.handle.net/10261/125048-
dc.description.abstractPeptides and oligodeoxynucleotides containing photolabile 2-nitrobenzyl groups as mid-sequences were prepared. Photocleavage of aqueous solutions of these compounds neared completion within 30 min to a few hours depending on the photolabile group used. A photolabile group was introduced in the loop of an intramolecular oligodeoxynucleotide hairpin. Melting curves of the hairpin with and without the complementary oligodeoxynucleotide showed a preference for the intramolecular hairpin form, but an intermolecular duplex was observed after photolysis. These results open the possibility of using photolabile DNA hairpins for the fabrication of patterned surfaces.es_ES
dc.language.isoenges_ES
dc.publisherJohn Wiley & Sonses_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccesses_ES
dc.subject2-nitrobenzyles_ES
dc.subjectAqueous solutionses_ES
dc.subjectDNA hairpines_ES
dc.subjectMelting curveses_ES
dc.subjectOligodeoxynucleotidees_ES
dc.subjectOligodeoxynucleotideses_ES
dc.subjectPatterned surfacees_ES
dc.subjectPhotocleavagees_ES
dc.titlePhotocleavage of peptides and oligodeoxynucleotides carrying 2-nitrobenzyl groupses_ES
dc.typeartículoes_ES
dc.identifier.doihttp://dx.doi.org/10.1002/hlca.200800361-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionDOI: 10.1002/hlca.200800361es_ES
dc.rights.licensehttp://www.sherpa.ac.uk/romeo/issn/0018-019X/es_ES
dc.relation.csices_ES
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