Solution structure and stability of a disulfide cross-linked nucleopeptide duplex
Autores
Gómez Pinto, Irene; Marchan Sancho, Vicente; Gago Badenas, Federico; Grandas, Anna; González, CarlosEditor
Royal Society of Chemistry
Fecha de publicación
2003Cita bibliográfica
CHEM. COMMUN. , 2003, 2558-2559
Tipo de documento
info:eu-repo/semantics/article
Versión
info:eu-repo/semantics/publishedVersion
Versión del editor
http://dx.doi.org/10.1039/B307300ADerechos de acceso
info:eu-repo/semantics/openAccess
Resumen
NMR methods are used to study the structure and stability of the duplex formed by the nucleopeptide [Ac- Cys- Gly- Ala-Hse( p(3')dGCATGC)- Ala-OH](2)[S-S], in which the oligonucleotide is self-complementary and the cysteine residues of the two peptide chains form a disulfide bridge; thermal transitions and NMR-derived structural calculations are consistent with a 3-D structure in which the oligonucleotide forms a standard B-DNA helix without significant distortions; the peptide chains are relatively disordered in solution and lie in the minor groove of the DNA helix; this nucleopeptide duplex exhibits a high melting temperature, indicating that peptide - oligonucleotide conjugates containing cysteines are suitable molecules to establish cross-links between DNA strands and stabilize the duplex.
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