RNA duplexes with biphenyl substituents as base replacements are less stable than DNA duplexes


Autoria(s): Brotschi, Christine; Leumann, Christian J.
Data(s)

2005

Resumo

Introduction of a hydrophobic biphenyl-C-nucleotide pair into a 11-mer RNA duplex is associated with a net penalty in the free energy of duplex formation of 2.0 kcal mol(-1) or 10 degrees C in T(m), relative to DNA. These differential stabilities are of relevance with respect to the transcriptional and translational aspects of hydrophobic base-pairs

Formato

application/pdf

Identificador

http://boris.unibe.ch/53097/1/reprint.pdf

Brotschi, Christine; Leumann, Christian J. (2005). RNA duplexes with biphenyl substituents as base replacements are less stable than DNA duplexes. Chemical communications(15), pp. 2023-2025. Royal Society of Chemistry 10.1039/B419278H <http://dx.doi.org/10.1039/B419278H>

doi:10.7892/boris.53097

info:doi:10.1039/B419278H

info:pmid:15834493

urn:issn:1359-7345

Idioma(s)

eng

Publicador

Royal Society of Chemistry

Relação

http://boris.unibe.ch/53097/

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Brotschi, Christine; Leumann, Christian J. (2005). RNA duplexes with biphenyl substituents as base replacements are less stable than DNA duplexes. Chemical communications(15), pp. 2023-2025. Royal Society of Chemistry 10.1039/B419278H <http://dx.doi.org/10.1039/B419278H>

Palavras-Chave #570 Life sciences; biology #540 Chemistry
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion

PeerReviewed