Polyanionic carboxyethyl peptide nucleic acids (ce-PNAs): Synthesis and DNA binding

14Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

Abstract

New polyanionic modifications of polyamide nucleic acid mimics were obtained. Thymine decamers were synthesized from respective chiral α- and γ-monomers, and their enantiomeric purity was assessed. Here, we present the decamer synthesis, purification and characterization by MALDI-TOF mass spectrometry and an investigation of the hybridization properties of the decamers. We show that the modified γ-S-carboxyethyl-T10 PNA forms a stable triplex with polyadenine DNA.

Cite

CITATION STYLE

APA

Kirillova, Y., Boyarskaya, N., Dezhenkov, A., Tankevich, M., Prokhorov, I., Varizhuk, A., … Pozmogova, G. (2015). Polyanionic carboxyethyl peptide nucleic acids (ce-PNAs): Synthesis and DNA binding. PLoS ONE, 10(10). https://doi.org/10.1371/journal.pone.0140468

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free