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Journal ArticleDOI

The First Analogues of LNA (Locked Nucleic Acids): Phosphorothioate-LNA and 2′-Thio-LNA

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TLDR
A 9-mer phosphorothioate-LNA with three LNA thymine monomers (1, X = O, Y = S, S, Base = thymin-1-yl) and nine-mer LNA with one, three or five 2-thio-Lna monomers were shown to recognize both complementary DNA and RNA with thermal affinities comparable to those of parent LNA as mentioned in this paper.
Abstract
LNA (Locked Nucleic Acids, 1, X = O, Y = O) is a novel oligonucleotide analogue capable of recognizing complementary DNA and RNA with unprecedented thermal affinities. Synthesis of the first chemically modified LNA analogues is reported. A 9-mer phosphorothioate-LNA containing three LNA thymine monomers (1, X = O, Y = S, Base = thymin-1-yl) and 9-mer LNAs containing one, three or five 2'-thio-LNA monomers (1, X = S, Y = O, Base = uracil-1-yl) were able to recognize both complementary DNA and RNA with thermal affinities comparable to those of parent LNA.

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References
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Journal ArticleDOI

The first analogues of LNA (locked nucleic acids): phosphorothioate-LNA and 2'-thio-LNA.

TL;DR: A 9-mer phosphorothioate-LNA containing three LNA thymine monomers were able to recognize both complementary DNA and RNA with thermal affinities comparable to those of parent LNA.
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