Synthesis and Improved Cross-Linking Properties of C5-Modified Furan Bearing PNAs.

ABSTRACT: Over the past decades, peptide nucleic acid/DNA (PNA:DNA) duplex stability has been improved via backbone modification, often achieved via introducing an amino acid side chain at the ?- or ?-position in the PNA sequence. It was previously shown that interstrand cross-linking can further enhance the binding event. In this work, we combined both strategies to fine-tune PNA crosslinking towards single stranded DNA sequences using a furan oxidation-based crosslinking method; for this purpose, ?-l-lysine and ?-l-arginine furan-PNA monomers were synthesized and incorporated in PNA sequences via solid phase synthesis. It was shown that the l-lysine ?-modification had a beneficial effect on crosslink efficiency due to pre-organization of the PNA helix and a favorable electrostatic interaction between the positively-charged lysine and the negatively-charged DNA backbone. Moreover, the crosslink yield could be optimized by carefully choosing the type of furan PNA monomer. This work is the first to describe a selective and biocompatible furan crosslinking strategy for crosslinking of ?-modified PNA sequences towards single-stranded DNA.

SUBMITTER: Elskens J 

PROVIDER: S-EPMC6150320 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature