| Literature DB >> 28332825 |
Chenguang Lou, Simone V Samuelsen, Niels Johan Christensen1, Birte Vester, Jesper Wengel.
Abstract
Mono- and diaminated 2'-amino-LNA monomers were synthesized and introduced into oligonucleotides. Each modification imparts significant stabilization of nucleic acid duplexes and triplexes, excellent sequence selectivity, and significant nuclease resistance. Molecular modeling suggested that structural stabilization occurs via intrastrand electrostatic attraction between the protonated amino groups of the aminated 2'-amino-LNA monomers and the host oligonucleotide backbone.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28332825 DOI: 10.1021/acs.bioconjchem.7b00061
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774